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thaliana","tax_id":3702}],"document_location":["DDESC","BSUMM","CLAIM"],"count":5379,"data_source":["USPTO_PSIPS"]},"has_sequence":true,"legal_status":{"ipr_type":"patent for invention","granted":true,"earliest_filing_date":"2001-08-24","grant_date":"2006-09-19","anticipated_term_date":"2023-03-23","discontinuation_date":"2018-10-22","has_disclaimer":false,"patent_status":"EXPIRED","publication_count":3,"has_spc":false,"has_grant_event":false,"has_entry_into_national_phase":false},"abstract":{"en":[{"text":"Clusters of plant genes that are regulated in response to one or more stress conditions are provided, as are isolated plant stress-regulated genes, including portions thereof comprising a coding sequence or a regulatory element, and to consensus sequences comprising a plant stress-regulated regulatory element. In addition, a recombinant polynucleotide, which includes a plant stress-regulated gene, or functional portion thereof, operatively linked to a heterologous nucleotide sequence, is provided, as are transgenic plants, which contain a plant stress-regulated gene or functional portion thereof that was introduced into a progenitor cell of the plant. Also provided are methods of using a plant stress-regulated gene to confer upon a plant a selective advantage to a stress condition, methods of identifying an agent that modulates the activity of a plant stress-regulated regulatory element, and methods of determining whether a plant has been exposed to a stress.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"}]},"abstract_lang":["en"],"has_abstract":true,"claim":{"en":[{"text":"1. An isolated polynucleotide, comprising SEQ ID NO: 1034.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"2. A recombinant nucleic acid molecule, comprising the isolated polynucleotide of claim 1 operatively linked to a heterologous nucleotide sequence.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"3. A vector, comprising the polynucleotide of claim 1 .","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"4. The vector of claim 3 , which is an expression vector.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"5. A cell containing the isolated polynucleotide of claim 1 .","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"},{"text":"6. The cell of claim 5 , which is a plant cell.","lang":"en","source":"USPTO_FULLTEXT","data_format":"ORIGINAL"}]},"claim_lang":["en"],"has_claim":true,"description":{"en":{"text":"This application claims the benefit under 35 U.S.C. 119(e) of U.S. Ser. No. 60/227,866, filed Aug. 24, 2000; U.S. Ser. No. 60/264,647, filed Jan. 26, 2001; and U.S. Ser. No. 60/300,111, filed Jun. 22, 2001, each of which is incorporated herein by reference in its entirety. Three CD-R compact discs, labeled “Copy 1”, “Copy 2”, and “CRF” and having the files listed below, are submitted herewith and are incorporated herein by reference. Copy 1 and Copy 2 each contain two text documents: 1) a file named SCRIP1300-3_SEQUENCE_LISTING, which contains the Sequence Listing, was created on Aug. 20, 2001 (and recorded on the CD-R on Aug. 21, 2001), and is 9,972 KB in size; and 2) a file named SCRIP1300-3_Table — 32, which contains Table 32, was created on Aug. 20, 2001 (and recorded on the CD-R on Aug. 21, 2001), and is 1,251 KB in size. The CRF contains a single file named SCRIP1300-3_SEQUENCE_LISTING, which contains the Sequence Listing, was created on Aug. 20, 2001 (and recorded on the CD-R on Aug. 21, 2001), is 9,972 KB in size, and is identical to the files having the same name on Copy 1 and Copy 2. BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates generally to plant genes, the expression of which are regulated in response to stress, and more specifically to the gene regulatory elements involved in a stress-induced response in plants, to uses of the coding sequences and regulatory elements of such plant stress-regulated genes, and to transgenic plants genetically modified to express such a coding sequence or to express a heterologous polynucleotide from such a regulatory element. 2. Background Information Microarray technology is a powerful tool that can be used to identify the presence and level of expression of a large number of polynucleotides in a single assay. A microarray is formed by linking a large number of discrete polynucleotide sequences, for example, a population of polynucleotides representative of a genome of an organism, to a solid support such as a microchip, glass slide, or the like, in a defined pattern. By contacting the microarray with a nucleic acid sample obtained from a cell of interest, and detecting those polynucleotides expressed in the cell can hybridize specifically to complementary sequences on the chip, the pattern formed by the hybridizing polynucleotides allows the identification of clusters of genes that are expressed in the cell. Furthermore, where each polynucleotide linked to the solid support is known, the identity of the hybridizing sequences from the nucleic acid sample can be identified. A strength of microarray technology is that it allows the identification of differential gene expression simply by comparing patterns of hybridization. For example, by comparing the hybridization pattern of nucleic acid molecules obtained from cells of an individual suffering from a disease with the nucleic acids obtained from the corresponding cells of a healthy individual, genes that are differentially expressed can be identified. The identification of such differentially expressed genes provides a means to identify new genes, and can provide insight as to the etiology of a disease. Microarray technology has been widely used to identify patterns of gene expression associated with particular stages of development or of disease conditions in animal model systems, and is being applied to the identification of specific patterns of gene expression in humans. The recent availability of information for the genomes of plants provides a means to adapt microarray technology to the study of plant gene expression. Plants and plant products provide the primary sustenance, either directly or indirectly, for all animal life, including humans. For the majority of the world's human population and for many animals, plants and plant products provide the sole source of nutrition. As the world population increases, the best hope to prevent widespread famine is to increase the quantity and improve the quality of food crops, and to make the crops available to the regions of the world most in need of food. Throughout history, a continual effort has been made to increase the yield and nutritious value of food crops. For centuries, plants having desirable characteristics such as greater resistance to drought conditions or increased size of fruit were crossbred and progeny plants exhibiting the desired characteristics were selected and used to produce seed or cuttings for propagation. Using such classical genetic methods, plants having, for example, greater disease resistance, increased yield, and better flavor have been obtained. The identification of plant genes involved in conferring a selective advantage on the plant to an environmental challenge would facilitate the generation and yield of plants, thereby increasing the available food supply to an increasing world population. The involvement of these genes in a single organism to responses to multiple stress conditions, however, remains unknown. Thus, a need exists to identify plant genes and polynucleotides that are involved in modulating the response of a plant to changing environmental conditions. The present invention satisfies this need and provides additional advantages. SUMMARY OF THE INVENTION The present invention relates to clusters of genes that are regulated in response to a stress condition in plants. Such clusters include, for example, plant polynucleotides whose expression is altered in response to two or more different stress conditions; and plant polynucleotides the expression of which are altered in response to one stress condition, but not to others. The identification of such clusters, using microarray technology, has allowed the identification of plant stress-regulated genes in Arabidopsis thaliana (see Tables 1 and 2); and homologs and orthologs thereof in other plant species (see Table 32). Thus, the invention provides isolated polynucleotide portions of Arabidopsis plant stress-regulated genes, and homologs and orthologs thereof; variants of such sequences, and polynucleotides encoding substantially similar plant stress-regulated polypeptides expressed therefrom. Such sequences include, for example, sequences encoding transcription factors; enzymes, including kinases; and structural proteins, including channel proteins (see Tables 29–31). Accordingly, the present invention also relates to an isolated polynucleotide comprising all or a portion of a plant stress-regulated gene, and to polynucleotide portions thereof, including a coding region (open reading frame), which encodes all or a portion of a stress-regulated polypeptide, for example, as set forth in SEQ ID NOS:1–2703; and a regulatory element involved in regulating the response of the plant to a stress condition such exposure to an abnormal level of salt, osmotic pressure, temperature or any combination thereof, for example, as set forth in SEQ ID NOS:2704–5379. The present invention also relates to a recombinant polynucleotide, which contains a nucleotide sequence of a plant stress-regulated gene or functional portion thereof operatively linked to a heterologous nucleotide sequence. In one embodiment, the recombinant polynucleotide comprises a plant stress-regulated gene regulatory element operatively linked to a heterologous nucleotide sequence, which is not regulated by the regulatory element in a naturally occurring plant. The heterologous nucleotide sequence, when expressed from the regulatory element, can confer a desirable phenotype to a plant cell containing the recombinant polynucleotide. In another embodiment, the recombinant polynucleotide comprises a coding region, or portion thereof, of a plant stress-regulated gene operatively linked to a heterologous promoter. The heterologous promoter provides a means to express an encoded stress-regulated polypeptide constitutively, or in a tissue-specific or phase-specific manner. Accordingly, in one aspect, the present invention provides an isolated polynucleotide comprising a nucleotide sequence of a plant gene that hybridizes under stringent conditions, preferably high stringency conditions, to any one of SEQ ID NOS:1–5379 (see Tables 1 and 2), including to a coding region (SEQ ID NOS:1–2703) or a regulatory region, which can alter transcription of an operatively linked nucleic acid sequence in response to an abiotic stress (SEQ ID NOS:2704–5379; see Table 2), or to a complement thereof. Additional aspects provide sequences that hybridize under stringent conditions, preferably high stringency conditions, to the complements of SEQ ID NO 1–1261 (cold responsive genes; Tables 3–6), SEQ ID NOS:2227–2427 (saline responsive genes; Tables 7–10), SEQ ID NOS:2428–2585 (osmotic responsive genes; Tables 11–14), SEQ ID NOS:1699–1969 (cold and osmotic responsive genes; Tables 15–17), SEQ ID NOS:1970–2226 (cold and saline responsive genes; Tables 18–20), SEQ ID NOS:2586–2703 (osmotic and saline responsive genes; Tables 21–23), and SEQ ID NOS:1262–1698 (cold, osmotic and saline responsive genes; Tables 24–26), and which can comprise regulatory regions that can alter transcription in response to cold stress, osmotic stress, saline stress, or combinations thereof (SEQ ID NOS:2704–5379; see Table 2). Also provided are nucleotide sequences complementary thereto, and expression cassettes, plants and seeds comprising any of the above isolated sequences. In another aspect, the present invention provides an isolated polynucleotide comprising a plant nucleotide sequence that hybridizes under stringent conditions, preferably high stringency conditions, to the complement of any one of SEQ ID NOS:1–2703 (Table 1), including to a coding region thereof (SEQ ID NOS:2704–5379), wherein expression of said coding region is altered in response to an abiotic stress. Additional aspects provide sequences that hybridize under high stringency conditions to the complements of SEQ ID NO 1–1261 (cold responsive genes; Tables 3–6), SEQ ID NOS:2227–2427 (saline responsive genes; Tables 7–10), SEQ ID NOS:2428–2585 (osmotic responsive genes; Tables 11–14), SEQ ID NOS:1699–1969 (cold and osmotic responsive genes; Tables 15–17), SEQ ID NOS:1970–2226 (cold and saline responsive genes; Tables 18–20), SEQ ID NOS:2586–2703 (osmotic and saline responsive genes; Tables 21–23), and SEQ ID NOS:1262–1698 (cold, osmotic and saline responsive genes; Tables 24–26), and which can comprise a coding region whose transcription is altered in response to cold stress, osmotic stress, saline stress, or a combination thereof. Also provided are nucleotide sequences complementary thereto, and expression cassettes, plants and seeds comprising any of the above sequences. The invention further relates to a method of producing a transgenic plant, which comprises at least one plant cell that exhibits altered responsiveness to a stress condition. In one embodiment, the method can be performed by introducing a polynucleotide portion of plant stress-regulated gene into a plant cell genome, whereby the polynucleotide portion of the plant stress-regulated gene modulates a response of the plant cell to a stress condition. The polynucleotide portion of the plant stress-regulated gene can encode a stress-regulated polypeptide or functional peptide portion thereof (see SEQ ID NOS:1–2703), wherein expression of the stress-regulated polypeptide or functional peptide portion thereof either increases the stress tolerance of the transgenic plant, or decreases the stress tolerance of the transgenic plant. The polynucleotide portion of the plant stress-regulated gene encoding the stress-regulated polypeptide or functional peptide portion thereof can be operatively linked to a heterologous promoter. The polynucleotide portion of the plant stress-regulated gene also can comprise a stress-regulated gene regulatory element (see SEQ ID NOS:2704–5379). The stress-regulated gene regulatory element can integrate into the plant cell genome in a site-specific manner, whereupon it can be operatively linked to a heterologous nucleotide sequence, which can be expressed in response to a stress condition specific for the regulatory element; or can be a mutant regulatory element, which is not responsive to the stress condition, whereby upon integrating into the plant cell genome, the mutant regulatory element disrupts an endogenous stress-regulated regulatory element of a plant stress-regulated gene, thereby altering the responsiveness of the plant stress-regulated gene to the stress condition. In one aspect, the invention provides a method for producing a transgenic plant by introducing into at least one plant cell a recombinant nucleic acid construct comprising i) all or a portion of any one of SEQ ID NOS:1–5379; ii) a polynucleotide comprising a coding region that hybridizes under conditions of high stringency to all or a portion of the complement of any one of SEQ ID NOS:1–2703; iii) a polynucleotide comprising a sequence that alters transcription of an operatively linked coding region in response to abiotic stress, and that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:2704–5379; iv) a polynucleotide having at least 90% sequence identity with any one of SEQ ID NO:1–5379; v) a fragment of any one of the sequences of iv), wherein the fragment comprises a coding region; or vi) a fragment of any one of the sequences of iv), wherein the fragment comprises a nucleotide sequence that alters transcription of an operatively linked coding region in response to abiotic stress; and regenerating a plant from the at least one plant cell. Another aspect provides a method for producing a transgenic plant comprising introducing into at least one plant cell a recombinant nucleic acid construct comprising i) any one of SEQ ID NOS:1–1261 or 2704–3955; ii) a polynucleotide comprising a coding region that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:1–1261; iii) a polynucleotide comprising a sequence that alters transcription of an operatively linked coding region in response to cold stress that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:2704–3955; iv) a polynucleotide that has at least 90% sequence identity with any one of SEQ ID NOS:1–1261 or 2704–3955; v) a fragment of any one of the sequences of iv), wherein the fragment comprises a coding region; or vi) a fragment of any one of the sequences of iv) wherein the fragment comprises a sequence or region that alters transcription of an operatively linked coding region in response to cold stress; and regenerating a plant from the at least one plant cell. In another aspect, the invention provides a method for producing a transgenic plant by introducing into at least one plant cell a recombinant nucleic acid construct comprising i) any one of SEQ ID NOS:2428–2585 or 5108–5263; ii) a polynucleotide comprising a coding region that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:2428–2585; iii) a polynucleotide comprising a sequence that alters transcription of an operatively linked coding region in response to osmotic stress that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:5108–5263; iv) a polynucleotide that has at least 90% sequence identity with any one of SEQ ID NOS:2428–2585 or 5108–5263; v) a fragment of any one of the sequences of iv), wherein the fragment comprises a coding region; or vi) a fragment of any one of the sequences of iv), wherein the fragment comprises a sequence or region that alters transcription of an operatively linked coding region in response to osmotic stress; and regenerating a plant from the at least one plant cell. Still another aspect provides a method for producing a transgenic plant comprising introducing into at least one plant cell a recombinant nucleic acid construct comprising i) any one of SEQ ID NOS:2227–2427 or 4910–5107; ii) a polynucleotide comprising a coding region that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:2227–2427; iii) a polynucleotide comprising a sequence that alters transcription of an operatively linked coding region in response to saline stress that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:2227–2427; iv) a polynucleotide that has at least 90% sequence identity with any one of SEQ ID NOS:4910–5107; v) a fragment of any one of the sequences of iv), wherein the fragment comprises a coding region; or vi) a fragment of any one of the sequences of iv) wherein the fragment comprises a sequence or region that alters transcription of an operatively linked coding region in response to saline stress; and regenerating a plant from the at least one plant cell. Yet another aspect provides a method for producing a transgenic plant comprising introducing into at least one plant cell a recombinant nucleic acid construct comprising i) any one of SEQ ID NOS:1699–1969 or 4389–4654; ii) a polynucleotide comprising a coding region that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:1699–1969; iii) a polynucleotide comprising a sequence that alters transcription of an operatively linked coding region in response to a combination of cold and osmotic stress that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:4389–4654; iv) a polynucleotide that has at least 90% sequence identity with any one of SEQ ID NOS:1699–1969 or 4389–4654; v) a fragment of any one of the sequences of iv), wherein the fragment comprises a coding region; or vi) a fragment of any one of the sequences of iv), wherein the fragment comprises a sequence or region that alters transcription of an operatively linked coding region in response to a combination of cold and osmotic stress; and regenerating a plant from the at least one plant cell. Yet another aspect provides a method for producing a transgenic plant comprising introducing into at least one plant cell a recombinant nucleic acid construct comprising i) any one of SEQ ID NOS:1970–2226 or 4655–4909; ii) a polynucleotide comprising a coding region that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:1970–2226; iii) a polynucleotide comprising a sequence that alters transcription of an operatively linked coding region in response to a combination of cold and saline stress that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:4655–4909; iv) a polynucleotide that has at least 90% sequence identity with any one of SEQ ID NOS:1970–2226 or 4655–4909; v) a fragment of any one of the sequences of iv), wherein the fragment comprises a coding region; or vi) a fragment of any one of the sequences of iv), wherein the fragment comprises a sequence or region that alters transcription of an operatively linked coding region in response to a combination of cold and saline stress; and regenerating a plant from the at least one plant cell. A further aspect provides a method for producing a transgenic plant comprising introducing into at least one plant cell a recombinant nucleic acid construct comprising i) any one of SEQ ID NOS:2586–2703 or 5264–5379; ii) a polynucleotide comprising a coding region that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:2586–2703; iii) a polynucleotide comprising a sequence that alters transcription of an operatively linked coding region in response to a combination of osmotic and saline stress that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS: 5264–5379; iv) a polynucleotide that has at least 90% sequence identity with any one of SEQ ID NOS:2586–2703 or 5264–5379; v) a fragment of any one of the sequences of iv), wherein the fragment comprises a coding region; or vi) a fragment of any one of the sequences of iv), wherein the fragment comprises a sequence or region that alters transcription of an operatively linked coding region in response to a combination of osmotic and saline stress; and regenerating a plant from the at least one plant cell. Another aspect provides a method for producing a transgenic plant comprising introducing into at least one plant cell a recombinant nucleic acid construct comprising i) any one of SEQ ID NOS:1262–1698 or 3956–4388; ii) a polynucleotide comprising a coding region that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:1262–1698; iii) a polynucleotide comprising a sequence that alters transcription of an operatively linked coding region in response to a combination of cold, osmotic and saline stress that hybridizes under conditions of high stringency to the complement of any one of SEQ ID NOS:3956–4388; iv) a polynucleotide that has at least 90% sequence identity with any one of SEQ ID NOS:1262–1698 or 3956–4388; v) a fragment of any one of the sequences of iv), wherein the fragment comprises a coding region; or vi) a fragment of any one of the sequences of iv) wherein the fragment comprises a sequence or region that alters transcription of an operatively linked coding region in response to a combination of cold, osmotic and saline stress; and regenerating a plant from the at least one plant cell. Further aspects include plants and uniform populations of plants made by the above methods as well as seeds and progeny from such plants. In another embodiment, a transgene introduced into a plant cell according to a method of the invention can encode a polypeptide that regulates expression from an endogenous plant stress-regulated gene. Such a polypeptide can be, for example, a recombinantly produced polypeptide comprising a zinc finger domain, which is specific for the regulatory element, and an effector domain, which can be a repressor domain or an activator domain. The polynucleotide encoding the recombinant polypeptide can be operatively linked to and expressed from a constitutively active, inducible or tissue specific or phase specific regulatory element. Expression of the recombinant polypeptide from a plant stress-regulated promoter as disclosed herein can be particularly advantageous in that the polypeptide can be coordinately expressed with the endogenous plant stress-regulated genes upon exposure to a stress condition. The invention also provides transgenic plants produced by a method as disclosed, as well as to a plant cell obtained from such transgenic plant, wherein said plant cell exhibits altered responsiveness to the stress condition; a seed produced by the transgenic plant; and a cDNA or genomic DNA library prepared from the transgenic plant, or from a plant cell from said transgenic plant, wherein said plant cell exhibits altered responsiveness to the stress condition. In one aspect, the invention provides an isolated nucleic acid molecule comprising a nucleotide sequence substantially similar to a sequence of any one of SEQ ID NOS:2704–5379, which can alter transcription of an operatively linked polynucleotide in a plant cell in response to an abiotic stress. Additional aspects of the invention provide isolated polynucleotides, including, for example, sequences substantially similar to any of SEQ ID NOS:2704–3955, which can alter transcription of an operatively linked polynucleotide in response to a cold stress; isolated polynucleotides substantially similar to a sequence of any of SEQ ID NOS:5108–5263, which can alter transcription of an operatively linked polynucleotide in response to an osmotic stress; isolated polynucleotides substantially similar to a sequence of any of SEQ ID NOS:4910–5107, which can alter transcription of an operatively linked polynucleotide in response to a saline stress; isolated polynucleotides substantially similar to a sequence of any of SEQ ID NOS:4389–4654, which can alter transcription of an operatively linked polynucleotide in response to a combination of cold and osmotic stresses; isolated polynucleotides substantially similar to a sequence of any of SEQ ID NOS:4655–4909, which can alter transcription of an operatively linked polynucleotide in response to a combination of cold and saline stresses; isolated polynucleotides substantially similar to a sequence of any of SEQ ID NOS:5264–5379, which can alter transcription of an operatively linked polynucleotide in response to a combination of osmotic and saline stresses; and isolated polynucleotides substantially similar to a sequence of any of SEQ ID NOS:3956–4388, which can alter transcription of an operatively linked polynucleotide in response to a combination of cold, osmotic and saline stresses. Related aspects of the invention provide an isolated nucleotide sequences that can alter transcription of an operatively linked polynucleotide in response to an abiotic stress, and that hybridize under stringent conditions, preferably highly stringent conditions, to the complement of any one of SEQ ID NOS:2704–5379. Additional aspects provide an isolated nucleotide sequence that can alter transcription of an operatively linked polynucleotide in response to cold stress, and that hybridizes under stringent conditions, preferably highly stringent conditions, to the complement of any one of SEQ ID NOS:2704–3955; a nucleotide sequence that alters transcription of an operatively linked polynucleotide in response to osmotic stress, and that hybridizes under stringent conditions, preferably highly stringent conditions, to the complement of any one of SEQ ID NOS:5108–5263; a nucleotide sequence that alters transcription of an operatively linked polynucleotide in response to saline stress, and that hybridizes under stringent conditions, preferably highly stringent conditions, to the complement of any one of SEQ ID NOS:4910–5107; a nucleotide sequence that alters transcription of an operatively linked polynucleotide in response to a combination of cold and osmotic stress, and that hybridizes under stringent conditions, preferably highly stringent conditions, to the complement of any one of SEQ ID NOS:4389–4654; a nucleotide sequence that alters transcription of an operatively linked polynucleotide in response to a combination of cold and saline stress, and that hybridizes under stringent conditions, preferably highly stringent conditions, to the complement of any one of SEQ ID NOS:4655–4909; a nucleotide sequence that alters transcription of an operatively linked polynucleotide in response to an combination of osmotic and saline stress, and that hybridizes under stringent conditions, preferably highly stringent conditions, to the complement of any one of SEQ ID NOS:5264–5379; and a nucleotide sequence that alters transcription of an operatively linked polynucleotide in response to a combination of cold, osmotic and saline stress, and that hybridizes under stringent conditions, preferably highly stringent conditions, to the complement of any one of SEQ ID NOS:3956–4388. Further aspects provide an expression cassette comprising as operatively linked components any of the above isolated nucleic acid sequences that alter transcription, a coding region, and a termination sequence. Also provided are host cells and seeds comprising such expression cassettes, plants containing such host cells and seeds and progeny of plants containing said host cells. In related aspects, the coding region of the expression cassettes comprise sequences encoding marker proteins and sequences involved in gene silencing such as antisense sequences, double stranded RNAi sequences, a triplexing agent, and sequences comprising dominant negative mutations. In additional related aspects, the coding regions comprise sequences encoding polypeptides that alter the response of a plant to an abiotic stress. The present invention also relates to a method of modulating the responsiveness of a plant cell to a stress condition. Such a method can be performed, for example, by introducing a polynucleotide portion of a plant stress-regulated genes described herein into the plant cell, thereby modulating the responsiveness of the plant cell to a stress condition. Such a method can result in the responsiveness of the plant cell being increased upon exposure to the stress condition, which, in turn, can result in increased or decreased tolerance of the plant cell to a stress condition; or can result in the responsiveness of the plant cell to the stress condition being decreased, which, in turn, can result in increased or decreased tolerance of the plant cell to a stress condition. In one embodiment, the polynucleotide portion of the plant stress-regulated gene can integrate into the genome of the plant cell, thereby modulating the responsiveness of the plant cell to the stress condition. In another embodiment, the polynucleotide portion of the plant stress-regulated gene encodes a stress-regulated polypeptide or functional peptide portion thereof, and can be operatively linked to a heterologous promoter. The polynucleotide portion of the plant stress-regulated gene also can contain a mutation, whereby upon integrating into the plant cell genome, the polynucleotide disrupts (knocks-out) an endogenous plant stress-regulated sequence, thereby modulating the responsiveness of the plant cell to the stress condition. Depending on whether the knocked-out gene encodes an adaptive or a maladaptive stress-regulated polypeptide, the responsiveness of the plant will be modulated accordingly. The present invention further relates to a method of modulating the activity of a biological pathway in a plant cell, wherein the pathway involves a stress-regulated polypeptide or a non-protein regulatory molecule. Such a method can be performed by introducing a polynucleotide portion of a plant stress-regulated gene, or a polynucleotide derived therefrom, for example a ribozyme derived from a nucleotide sequence as set forth in any of SEQ ID NOS:1–2703, into the plant cell, thereby modulating the activity of the biological pathway. The method can be performed with respect to a pathway involving any of the stress-regulated polypeptides as disclosed herein or encoded by the polynucleotides disclosed herein, as well as using homologs or orthologs thereof. In one embodiment, the method is performed by introducing a polynucleotide portion of a plant stress-regulated gene into the plant cell, wherein the plant stress-regulated gene comprises a nucleotide sequence as set forth in any of SEQ ID NOS:1–155, 157–228, 230–232, 234–557, 559–572, 574–605, 607–634, 636–786, 788–812, 814–1262, 1264–1386, 1387–1390, 1392–1404, 1406–1444, 1446–1483, 1485–1588, 1590–1608, 1610–1633, 1634–1725, 1727–1865, 1867–1917, 1919–1927, 1929–2855, 2857–2928, 2930–2932, 2934–3256, 3258–3271, 3273–3304, 3306–3323, 3325–3333, 3335–3485, 3487–3511, 3313–3956, 3958–4078, 4080–4097, 4099–4136, 4138–4175, 4177–4279, 4281–4299, 4301–4324, 4326–4414, 4416–4552, 4554–4602, and 4604–5379, thereby modulating the activity of the biological pathway. The present invention also relates to a method of identifying a polynucleotide that modulates a stress response in a plant cell. In one embodiment the method comprises determining gene expression in a plant exposed to at least one stress to produce an expression profile and identifying sequences whose expression is altered at least two fold compared to plants not exposed to the stress. Such an expression profile can be obtained, for example, by contacting an array of probes representative of a plant cell genome with nucleic acid molecules expressed in a plant cell exposed to the stress; and detecting one or more nucleic acid molecules expressed at a level different from a level of expression in the absence of the stress. The method can further comprise introducing the differentially expressed nucleic acid molecule into a plant cell; and detecting a modulated response of the genetically modified plant cell to a stress, thereby identifying a polynucleotide that modulates a stress response in a plant cell. The stress can be any stress, for example, an abiotic stress such as exposure to an abnormal level of cold, osmotic pressure, and salinity. The contacting is under conditions that allow for selective hybridization of a nucleic acid molecule with probe having sufficient complementarity, for example, under stringent hybridization conditions. Expression of the nucleic acid molecule can increase or decrease the tolerance of the plant cell to the stress, and the nucleic acid molecule can be expressed at a level that is less than or greater than the level of expression in the absence of the stress. In still another embodiment, the polynucleotide portion of the plant stress-regulated gene can comprise a stress-regulated regulatory element, which can be operatively linked to a heterologous nucleotide sequence, the expression of which can modulate the responsiveness of the plant cell to a stress condition. Such a heterologous nucleotide sequence can encode, for example, a stress-inducible transcription factor such as DREB1A. The heterologous nucleotide sequence also can encode a polynucleotide that is specific for a plant stress-regulated gene, for example, an antisense molecule, an RNAi molecule, a ribozyme, and a triplexing agent, any of which, upon expression in the plant cell, reduces or inhibits expression of a stress-regulated polypeptide encoded by the gene, thereby modulating the responsiveness of the plant cell to a stress condition, for example, an abnormal level of cold, osmotic pressure, and salinity. In another aspect, the method can include introducing a polynucleotide portion of a plant stress-regulated gene into the plant cell, wherein the plant stress-regulated gene includes a nucleotide sequence of a polynucleotide as set forth in any of SEQ ID NOS:1–155, 157–228, 230–232, 234–557, 559–572, 574–605, 607–634, 636–786, 788–812, 814–1262, 1264–1386, 1387–1390, 1392–1404, 1406–1444, 1446–1483, 1485–1588, 1590–1608, 1610–1633, 1634–1725, 1727–1865, 1867–1917, 1919–1927, 1929–2855, 2857–2928, 2930–2932, 2934–3256, 3258–3271, 3273–3304, 3306–3323, 3325–3333, 3335–3485, 3487–3511, 3313–3956, 3958–4078, 4080–4097, 4099–4136, 4138–4175, 4177–4279, 4281–4299, 4301–4324, 4326–4414, 4416–4552, 4554–4602, and 4604–5379, thereby modulating the responsiveness of the plant cell to a stress condition. The invention also relates to a plant cell obtained by any of the methods of modulating the responsiveness of a plant to a stress condition or combination of stress conditions, and to a plant comprising such a plant cell. The present invention further relates to a method of selecting a plant having an altered resistance to an abiotic stress condition or a combination of abiotic stress conditions, such a method being useful for marker-assisted breeding. Such a method can be performed, for example, by contacting nucleic acid molecules representative of expressed polynucleotides in a plant cell of a plant to be examined for having an altered resistance to an abiotic stress with a nucleic acid probes that selectively hybridizes under stringent conditions to a plant stress-regulated gene comprising a nucleotide sequence as set forth in any of SEQ ID NO:1–5379; detecting a level of selective hybridization of the nucleic acid probes to a nucleic acid molecule representative of an expressed polynucleotide in the plant cell, wherein the level of selective hybridization corresponds to the level of the expressed polynucleotide in the plant cell, which is indicative of resistance of the plant to an abiotic stress; and selecting a plant having a level of expression of a polynucleotide indicative of altered resistance to an abiotic stress condition. For example, the abiotic stress condition can be cold stress, and the nucleic acid probe can include at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1–1261 and 2704–3955, for example, at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1–155, 157–228, 230–232, 234–557, 559–572, 574–605, 607–634, 636–786, 788–812, 814–1261, 2704–2855, 2857–2928, 2930–2932, 2934–3256, 3258–3271, 3273–3304, 3306–3323, 3325–3333, 3335–3485, 3487–3511, and 3313–3955; or the abiotic stress condition can be saline stress, and the nucleic acid probe can include at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:2226–2427 and 4910–5107; or the abiotic stress condition can be osmotic stress, and the nucleic acid probe can include at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:2428–2585 and 5108–5263. In addition, a combination of abiotic stress conditions can be a combination of cold stress and osmotic stress, and the nucleic acid probe can include at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1669–1969 and 4389–4654, for example, at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1699–1725, 1727–1865, 1867–1917, 1919–1927, 1929–1969, 4389–4414, 4416–4552, 4554–4602, 4604–4612, and 4613–4654; or the combination of abiotic stress conditions can be a combination of cold stress and saline stress, and the nucleic acid probe can include at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS: 1970–2226 and 4655–4909; or the combination of abiotic stress conditions can be a combination of osmotic stress and saline stress, and the nucleic acid probe can include at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:2586–2703 and 5264–5379; or the combination of abiotic stress conditions can be a combination of cold stress, osmotic stress and saline stress, and the nucleic acid probe can include at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1262–1698 and 3956–4388, for example, at least about 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1262, 1264–1386, 1387–1390, 1392–1404, 1406–1444, 1446–1483, 1485–1588, 1590–1608, 1610–1633, 1634–1698, 3956, 3958–4078, 4080–4097, 4099–4136, 4138–4175, 4177–4279, 4281–4299, 4301–4324, and 4326–4388. The present invention also relates to a method of expressing a heterologous nucleotide sequence in a plant cell. Such a method can be performed, for example, by introducing into the plant cell a plant stress-regulated regulatory element operatively linked to the heterologous nucleotide sequence, whereby, upon exposure of the plant cell to a stress condition, the heterologous nucleotide sequence is expressed in the plant cell. In one embodiment, the stress-regulated gene regulatory element is any of the sequences described herein that are capable of altering transcription of an operatively linked sequence in response to an abiotic stress, for example, SEQ ID NOS:2704–5379. In another embodiment, stress-regulated gene regulatory element comprises a nucleotide sequence as set forth in any of SEQ ID NOS:2704–2855, 2857–2928, 2930–2932, 2934–3256, 3258–3271, 3273–3304, 3306–3323, 3325–3333, 3335–3485, 3487–3511, 3313–3956, 3958–4078, 4080–4097, 4099–4136, 4138–4175, 4177–4279, 4281–4299, 4301–4324, 4326–4414, 4416–4552, 4554–4602, and 4604–5379, whereby, upon exposure of the plant cell to stress condition, the heterologous nucleotide sequence is expressed in the plant cell. The heterologous nucleotide sequence can encode a selectable marker, a diagnostic marker, or a polypeptide that confers a desirable trait upon the plant cell, for example, a polypeptide that improves the nutritional value, digestibility or ornamental value of the plant cell, or a plant comprising the plant cell. The present invention additionally relates to a method of identifying a stress condition to which a plant cell was exposed by comparing an expression profile from a test plant suspected of having been exposed to at least one stress condition to an expression profile obtained from a reference plant, preferably of the same species, which has been exposed to the suspected stress condition. Such a method can be performed, for example, by contacting nucleic acid molecules representative of expressed polynucleotides in cells of the test plant with at least one nucleic acid probe under conditions suitable for selective hybridization to a complementary nucleotide sequence, wherein the probe comprises at least 15 nucleotides of a plant stress-regulated gene, wherein the stress-regulated gene does not have a nucleotide sequence of a polynucleotide as set forth in any of SEQ ID NOS:156, 229, 233, 558, 573, 606, 635, 787, 813, 1263, 1386, 1391, 1405, 1445, 1484, 1589, 1609, 1634, 1726, 1866, 1918 or 1928, or a nucleotide sequence complementary thereto, whereby detecting selective hybridization of at least one nucleic acid probe, or detecting a change in a level of selective hybridization as compared to a level of selective hybridization obtained using nucleic acid molecules representative of expressed polynucleotides in cells of a plant known not have been exposed to an abiotic stress, indicates that the test plant has been exposed to an abiotic stress, and whereby an absence of selective hybridization of at least one nucleic acid probe indicates that the test plant has not been exposed to an abiotic stress. For example, the abiotic stress is cold stress, and the probe can include at least 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1–155, 157–228, 230–232, 234–557, 559–572, 574–605, 607–634, 636–786, 788–812, 814–1261 or a nucleotide sequence complementary thereto; or the abiotic stress can be a saline stress, and the probe can include at least 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:2226–2427 or a nucleotide sequence complementary thereto; or the abiotic stress can be an osmotic stress, and the probe can include at least 15 nucleotides of a nucleotide sequence as set forth in two or more of SEQ ID NOS:2428–2585 or a nucleotide sequence complementary thereto. A method of identifying a stress condition to which a plant cell was exposed also can be performed, for example, by contacting nucleic acid molecules expressed in the test plant cell with an array of probes representative of the plant cell genome; detecting a profile of expressed nucleic acid molecules characteristic of a stress response, and comparing the expression pattern in the test plant to the expression pattern obtained from a reference plant thereby identifying the stress condition to which the plant cell was exposed. The contacting is under conditions that allow for selective hybridization of a nucleic acid molecule with probes having sufficient complementarity, for example, under stringent hybridization conditions. The profile can be characteristic of exposure to a single stress condition, for example, an abnormal level of cold, osmotic pressure, or salinity, or can be characteristic of exposure to more than one stress condition, for example, cold, increased osmotic pressure and increased salinity. In one embodiment, the nucleotide sequence of a gene whose expression is detected is selected from a polynucleotide comprising any of SEQ ID NOS:1–2703. In further embodiments, the nucleotide sequence of a gene that is expressed in response a particular stress or combination of stresses can comprise a polynucleotide expressed in response to cold stress (SEQ ID NOS:1–1261), osmotic stress (SEQ ID NOS:2428–2585), saline (salt) stress (SEQ ID NOS:2227–2427), a combination of cold and osmotic stress (SEQ ID NOS:1699–1969), a combination of saline and osmotic stress (SEQ ID NOS:1970–2226), a combination of osmotic and saline stress (SEQ ID NOS:2586–2703), or a combination of cold, osmotic and saline stress (SEQ ID NOS:1262–1698). In another embodiment, the method can be used for determining whether a test plant has been exposed to a combination of abiotic stress conditions. Such a method can be performed, for example, by contacting nucleic acid molecules representative of expressed polynucleotides in cells of the test plant with at least one nucleic acid probe under conditions suitable for selective hybridization to a complementary nucleotide sequence, whereby detecting selective hybridization of at least one nucleic acid probe, or detecting a change in a level of selective hybridization as compared to a level of selective hybridization obtained using nucleic acid molecules representative of expressed polynucleotides in cells of a plant known not have been exposed to a combination of stress conditions, indicates that the test plant has been exposed to a combination of abiotic stress conditions, and whereby an absence of selective hybridization of at least one nucleic acid probe indicates that the test plant has not been exposed to a combination of abiotic stress conditions. For example, the combination of abiotic stress conditions can be a combination of a cold stress and an osmotic stress, and the probe can include at least 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1699–1969, or a nucleotide sequence complementary thereto; or the combination of abiotic stress conditions can be a combination of a cold stress and a saline stress, and the probe can include at least 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1970–2226, or a nucleotide sequence complementary thereto; or the combination of abiotic stress conditions can be a combination of an osmotic stress and a saline stress, and the probe can included at least 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:2586–2703, or a nucleotide sequence complementary thereto; or the combination of abiotic stress conditions can be a combination of a cold stress, a saline stress and an osmotic stress, and the probe can include at least 15 nucleotides of a nucleotide sequence as set forth in any of SEQ ID NOS:1262–1698, or a nucleotide sequence complementary thereto. The present invention also relates to a method for monitoring a population of plants for exposure to a stress condition or combination of stress conditions. Such a method can be performed, for example, by introducing into the population of a plants a sentinel plant, wherein said sentinel plant is a transgenic plant, which contains plant cells containing a stress-regulated regulatory element operatively linked to a polynucleotide encoding a detectable marker; and examining the sentinel plant for expression of the detectable marker, which is indicative of exposure of the population of plants to a stress condition or combination of stress conditions. The stress condition or combination of stress conditions can be any such condition or conditions, particularly an abiotic stress condition or combination of abiotic stress conditions. The detectable marker can be any reporter molecule that is readily or conveniently detectable, particularly a marker that is visibly detectable, for example, a luminescent detectable marker such as luciferin, or a fluorescent detectable marker such as a green fluorescent protein, a yellow fluorescent protein, a cyan fluorescent protein, a red fluorescent protein, or an enhanced or modified form thereof. The present invention further relates to a transgenic plant, which contains a nucleic acid construct comprising a polynucleotide portion of plant stress-regulated polynucleotide. In one embodiment, the transgenic plant exhibits altered responsiveness to a stress condition as compared to a corresponding reference plant not containing the construct. Such a transgenic plant can contain, for example, a construct that disrupts an endogenous stress-regulated gene in the plant, thereby reducing or inhibiting expression of the gene in response to a stress condition. Such a knock-out can increase or decrease tolerance of the plant to a stress condition. The transgene also can comprise a coding sequence of a plant stress-regulated gene, which can be operatively linked to a heterologous regulatory element such as a constitutively active regulatory element, an regulated regulatory element, a tissues specific or phase specific regulatory element, or the like. In another embodiment, the transgenic plant contains a nucleic acid construct comprising a plant stress-regulated regulatory element, which can be operatively linked to a heterologous nucleotide sequence that can encode a polypeptide. Expression of the heterologous polypeptide can confer a desirable characteristic on the plant, for example, can improve the nutritional or ornamental value of the transgenic plant. In still another embodiment, the transgenic plant contains multiple nucleic acid constructs, which can be multiple copies of the same construct, or can be two or more different constructs. The present invention also relates to a plant stress-regulated regulatory element, which is obtained from a plant stress-regulated polynucleotide disclosed herein for example any of SEQ ID NOS:2704–5379; a homolog or ortholog thereof The invention also provides a method of identifying an agent, for example a transcription factor, that specifically binds to or activates a plant stress-regulated regulatory element. Such a method can be performed, for example, by contacting the regulatory element with a plant cell extract, and identifying polypeptides that specifically bind to the regulatory element. Confirmation that the specifically binding polypeptide is a transcription factor can be demonstrated using, for example, the stress-regulated regulatory element operably linked to a reporter gene, and detecting expression of the reporter gene. Control constructs comprising a regulatory element, other than a plant stress-regulated regulatory element, operatively linked to a reporter molecule can be used to confirm that the transcription factor is specific for the plant stress-regulated regulatory element. A polynucleotide encoding such a transcription factor also can be obtained. The present invention also relates to a method of using a polynucleotide portion of a plant stress-regulated gene to confer a selective advantage on a plant cell. In one embodiment, such a method is performed by introducing a plant stress-regulated regulatory element into a plant cell such as those described herein, wherein, upon exposure of the plant cell to a stress condition to which the regulatory element is responsive, a nucleotide sequence operatively linked to the regulatory element is expressed, thereby conferring a selective advantage to plant cell. The operatively linked nucleotide sequence can be, for example, a transcription factor, the expression of which induces the further expression of polynucleotides involved in a stress response, thereby enhancing the response of a plant to the stress condition. In another embodiment, a coding sequence of a plant stress-regulated gene as disclosed herein is introduced into the cell, thereby providing the plant with a selective advantage in response to a stress condition. In still another embodiment, the method results in the knock-out of a plant stress-regulated gene as disclosed herein in a first population of plants, thereby providing a selective advantage to a stress condition in a second population of plants. The invention further relates to a method of identifying an agent that modulates the activity of a stress-regulated regulatory element of a plant. In a particular embodiment, is provided a method for identifying an agent that alters the activity of an abiotic stress responsive regulatory element comprising contacting the agent or a composition containing an agent to be tested with at least one abiotic stress responsive regulatory element, preferably selected from the group consisting of SEQ ID NOS:2704–5379 (see Table 2), and determining the effect of the agent on the ability of the regulatory sequence to regulate transcription. In further embodiments, the regulatory elements are associated with particular stresses or combination of stresses such as cold stress (SEQ ID NOS:2704–3955), osmotic stress (SEQ ID NOS:5108–5263), saline stress (SEQ ID NOS:4910–5107), a combination of cold and osmotic stress (SEQ ID NOS:4389–4654), a combination of cold and saline stress (SEQ ID NOS:4655–4909), a combination of osmotic and saline stress (SEQ ID NOS:5264–5379), or a combination of cold, osmotic and saline stress (SEQ ID NOS:3956–4388). In one embodiment, the regulatory element can be operatively linked to a heterologous polynucleotide encoding a reporter molecule, and an agent that modulates the activity of the stress-regulated regulatory element can be identified by detecting a change in expression of the reporter molecule due to contacting the regulatory element with the agent. Such a method can be performed in vitro in a plant cell-free system, or in a plant cell in culture or in a plant in situ. In another embodiment, the agent is contacted with a transgenic plant containing an introduced plant stress-regulated regulatory element, and an agent that modulates the activity of the regulatory element is identified by detecting a phenotypic change in the transgenic plant. The methods of the invention can be performed in the presence or absence of the stress condition to which the particularly regulatory element is responsive. Another aspect provides a method for identifying an agent that alters abiotic stress responsive polynucleotide expression in a plant or plant cell comprising contacting a plant or plant cell with a test agent; subjecting the plant cell or plant cell to an abiotic stress or combination of stresses before, during or after contact with the agent to be tested; obtaining an expression profile of the plant or plant cell and comparing the expression profile of the plant or plant cell to an expression profile from a plant or plant cell not exposed to the abiotic stress or combination of stresses. In one embodiment, the expression profile comprises expression data for at least one nucleotide sequence comprising any of SEQ ID NOS:1–5379 (see Tables 1 and 2). In additional embodiments, the expression profile comprises expression data for at least one, and preferably two or more sequences associated with a particular abiotic stress or combination of stresses such as cold stress (SEQ ID NOS:1–1261 and 2704–3955), osmotic stress (SEQ ID NOS:2428–2585 and 5108–5263), saline stress (SEQ ID NOS:2227–2427 and 4910–5107), a combination of cold and osmotic stress (SEQ ID NOS:1699–1969 and 4389–4654), a combination of cold and saline stress (SEQ ID NOS:1970–2226 and 4655–4909), a combination of osmotic and saline stress (SEQ ID NOS:2586–2703 and 5264–5379), or a combination of cold, osmotic and saline stress (SEQ ID NOS:1262–1698 and 3956–4388). Still another aspect provides nucleotide probes useful for detecting an abiotic stress response in plants, the probes comprising a nucleotide sequence of at least 15, 25, 50 or 100 nucleotides that hybridizes under stringent, preferably highly stringent, conditions to at least one sequence comprising any of SEQ ID NOS:1–2703. Also provided are nucleotide probes comprising at least 15, 25, 50 or 100 nucleotides in length that hybridize under stringent, preferably highly stringent conditions, to at least one gene associated with a particular stress or combination of stresses, for example cold stress, (SEQ ID NOS:1–1261), osmotic stress (SEQ ID NOS:2428–2585), saline stress (SEQ ID NOS:2227–2427), a combination of cold and osmotic stress (SEQ ID NOS:1699–1969), a combination of cold and saline stress (SEQ ID NOS: 1970–2226), a combination of osmotic and saline stress (SEQ ID NOS:2586–2703), or a combination of cold, osmotic, and saline stress (SEQ ID NOS:1262–1698). An additional aspect provides a method for marker-assisted breeding to select plants having an altered resistance to abiotic stress comprising obtaining nucleic acid molecules from the plants to be selected; contacting the nucleic acid molecules with one or more probes that selectively hybridize under stringent, preferably highly stringent, conditions to a nucleic acid sequence selected from the group consisting of SEQ ID NOS:1–2703; detecting the hybridization of the one or more probes to the nucleic acid sequences wherein the presence of the hybridization indicates the presence of a gene associated with altered resistance to abiotic stress; and selecting plants on the basis of the presence or absence of such hybridization. Marker-assisted selection can also be accomplished using one or more probes which selectively hybridize under stringent, preferably highly stringent conditions, to a nucleotide sequence comprising a polynucleotide expressed in response associated with a particular stress, for example, a nucleotide sequence comprising any of SEQ ID NOS:1–1261 (cold stress), SEQ ID NOS:2428–2585 (osmotic stress), SEQ ID NOS:2227–2427 (saline stress), SEQ ID NOS:1699–1969 (cold and osmotic stress), SEQ ID NOS:1970–2226 (cold and saline stress), SEQ ID NOS:2586–2703 (osmotic and saline stress), or SEQ ID NOS:1262–1698 (cold, osmotic and saline stress). In each case marker-assisted selection can be accomplished using a probe or probes to a single sequence or multiple sequences. If multiple sequences are used they can be used simultaneously or sequentially. A further aspect provides a method for monitoring a population of plants comprising providing at least one sentinel plant containing a recombinant polynucleotide comprising a stress responsive regulatory sequence selected from the group consisting of SEQ ID NOS:2704–5379 which is operatively linked to a nucleotide sequence encoding a detectable marker, for example a fluorescent protein. Additional aspects provide the use of various regulatory sequences including those associated with cold stress (SEQ ID NOS:2704–3955), osmotic stress (SEQ ID NOS:5108–5263), saline stress (SEQ ID NOS:4910–5107), cold and osmotic stress (SEQ ID NOS:4389–4654), cold and saline stress (SEQ ID NOS:4655–4909), osmotic and saline stress (SEQ ID NOS:5264–5379), and cold, osmotic and saline stress (SEQ ID NOS:3956–4388), or fragments thereof wherein such fragments can alter transcription of an operatively linked nucleotide sequence in response to an abiotic stress. A further aspect provides a computer readable medium having stored thereon computer executable instructions for performing a method comprising receiving data on gene expression in a test plant of at least one nucleic acid molecule having at least 70%, preferably at least 80%, more preferably at least 90%, and most preferably at least 95% nucleotide sequence identity to one or more polynucleotide sequences as set forth in any of SEQ ID NOS:1–2703; and comparing expression data from the test plant to expression data for the same polynucleotide sequence or sequences in a plant that has been exposed to at least one abiotic stress. Yet a further aspect provides a computer readable medium having stored thereon a data structure comprising, sequence data for at least one, and preferably a plurality of nucleic acid molecules having at least 70%, preferably at least 80%, more preferably at least 90%, and most preferably at least 95% nucleotide sequence identity to a polynucleotide comprising any of SEQ ID NOS:1–2703, or the complement thereof; and a module receiving the nucleic acid molecule sequence data which compares the nucleic acid molecule sequence data to at least one other nucleic acid sequence. DETAILED DESCRIPTION OF THE INVENTION The present invention relates to clusters of genes that are induced in response to one or a combination of abiotic stress conditions. Abiotic stress conditions, such as a shortage or excess of solar energy, water and nutrients, and salinity, high and low temperature, or pollution (e.g., heavy metals), can have a major impact on plant growth and can significantly reduce the yield, for example, of cultivars. Under conditions of abiotic stress, the growth of plant cells is inhibited by arresting the cell cycle in late G1, before DNA synthesis, or at the G2/M boundary (see Dudits, Plant Cell Division, Portland Press Research, Monograph; Francis, Dudits, and Inze, eds., 1997; chap. 2, page 21; Bergounioux, Protoplasma 142:127–136, 1988). The identification of stress-regulated gene clusters, using microarray technology, provides a means to identify plant stress-regulated genes. As used herein, the term “cluster,” when used in reference to stress-regulated genes, refers to nucleotide sequences of genes that have been selected by drawing Venn diagrams, and selecting those genes that are regulated only by a selected stress condition. In general, a cluster of stress-regulated genes includes at least 5, 10, 15, or 20 genes, including polynucleotide portions thereof, each of which is responsive to the same selected stress condition or conditions. The selected stress condition can be a single stress condition, for example, cold, osmotic stress or salinity stress (see Tables 3–14), or can be a selected combination of stress conditions, for example, cold, osmotic stress and salinity stress (see Tables 15–26). In addition, a cluster can be selected based on specifying that all of the genes are coordinately regulated, for example, they all start at a low level and are induced to a higher level. However, a cluster of saline stress-regulated genes, for example, that was selected for coordinate regulation from low to high, also can be decreased in response to cold or mannitol. By varying the parameters used for selecting a cluster of gene nucleotide sequences, those genes that are expressed in a specific manner following a stress can be identified. As used herein in reference to a polynucleotide or polynucleotide portion of a gene or nucleic acid molecule, the term “isolated” means a polynucleotide, polynucleotide portion of a gene, or nucleic acid molecule that is free of one or both of the nucleotide sequences that normally flank the polynucleotide in a genome of a naturally-occurring organism from which the polynucleotide is derived. The term includes, for example, a polynucleotide or fragment thereof that is incorporated into a vector or expression cassette; into an autonomously replicating plasmid or virus; into the genomic DNA of a prokaryote or eukaryote; or that exists as a separate molecule independent of other polynucleotides. It also includes a recombinant polynucleotide that is part of a hybrid polynucleotide, for example, one encoding a polypeptide sequence. The terms “polynucleotide,” “oligonucleotide,” and “nucleic acid sequence” are used interchangeably herein to refer to a polymeric (2 or more monomers) form of nucleotides of any length, either ribonucleotides or deoxyribonucleotides. Although nucleotides are usually joined by phosphodiester linkages, the term also includes polymers containing neutral amide backbone linkages composed of aminoethyl glycine units. The terms are used only to refer to the primary structure of the molecule. Thus, the term includes double stranded and single stranded DNA molecules, including a sense strand or an antisense strand, and RNA molecules as well as genomic DNA, cDNA, mRNA and the like. It will be recognized that such polynucleotides can be modified, for example, by including a label such as a radioactive, fluorescent or other tag, by methylation, by the inclusion of a cap structure, by containing a substitution of one or more of the naturally occurring nucleotides with a nucleotide analog, by containing an internucleotide modification such as having uncharged linkages (e.g., methyl phosphonates, phosphotriesters, phosphoramidates, carbamates, or the like), by containing a pendant moiety such as a protein (e.g., a nuclease, toxin, antibody, signal peptide, poly-L-lysine, or the like), by containing an intercalator such as acridine or psoralen, by containing a chelator, which can be a metal such as boron, an oxidative metal, or a radioactive metal, by containing an alkylator, or by having a modified linkage (e.g., an alpha anomeric nucleic acid). The term “recombinant nucleic acid molecule” refers to a polynucleotide produced by human intervention. A recombinant nucleic acid molecule can contain two or more nucleotide sequences that are linked in a manner such that the product is not found in a cell in nature. In particular, the two or more nucleotide sequences can be operatively linked and, for example, can encode a fusion polypeptide, or can comprise a nucleotide sequence and a regulatory element. A recombinant nucleic acid molecule also can be based on, but different, from a naturally occurring polynucleotide, for example, a polynucleotide having one or more nucleotide changes such that a first codon, which normally is found in the polynucleotide, is replaced with a degenerate codon that encodes the same or a conservative amino acid, or such that a sequence of interest is introduced into the polynucleotide, for example, a restriction endonuclease recognition site or a splice site, a promoter, a DNA replication initiation site, or the like. As used herein, the term “abiotic stress” or “abiotic stress condition” refers to the exposure of a plant, plant cell, or the like, to a non-living (“abiotic”) physical or chemical agent or condition that has an adverse effect on metabolism, growth, development, propagation and/or survival of the plant (collectively “growth”). An abiotic stress can be imposed on a plant due, for example, to an environmental factor such as water (e.g., flooding, drought, dehydration), anaerobic conditions (e.g., a low level of oxygen), abnormal osmotic conditions, salinity or temperature (e.g., hot/heat, cold, freezing, frost), a deficiency of nutrients or exposure to pollutants, or by a hormone, second messenger or other molecule. Anaerobic stress, for example, is due to a reduction in oxygen levels (hypoxia or anoxia) sufficient to produce a stress response. A flooding stress can be due to prolonged or transient immersion of a plant, plant part, tissue or isolated cell in a liquid medium such as occurs during monsoon, wet season, flash flooding or excessive irrigation of plants, or the like. A cold stress or heat stress can occur due to a decrease or increase, respectively, in the temperature from the optimum range of growth temperatures for a particular plant species. Such optimum growth temperature ranges are readily determined or known to those skilled in the art. Dehydration stress can be induced by the loss of water, reduced turgor, or reduced water content of a cell, tissue, organ or whole plant. Drought stress can be induced by or associated with the deprivation of water or reduced supply of water to a cell, tissue, organ or organism. Saline stress (salt stress) can be associated with or induced by a perturbation in the osmotic potential of the intracellular or extracellular environment of a cell. Osmotic stress also can be associated with or induced by a change, for example, in the concentration of molecules in the intracellular or extracellular environment of a plant cell, particularly where the molecules cannot be partitioned across the plant cell membrane. As disclosed herein, clusters of plant stress-regulated genes (Example 1; see, also, Tables 1–31) and homologs and orthologs thereof (Table 32) have been identified. Remarkably, several of the stress-regulated genes previously were known to encode polypeptides having defined cellular functions, including roles as transcription factors, enzymes such as kinases, and structural proteins such as channel proteins (see Tables 29–31). The identification of Arabidopsis stress-regulated genes provides a means to identify homologous and orthologous genes and gene sequences in other plant species using well known procedures and algorithms based on identity (or homology) to the disclosed sequences. Thus, the invention provides polynucleotide sequences comprising plant stress-regulated genes that are homologs or orthologs, variants, or otherwise substantially similar to the polynucleotides disclosed herein, and having an E value≦1×10 −8 , which can be identified, for example, by a BLASTN search using the Arabidopsis polynucleotides of Tables 1 and 2 (SEQ ID NOS:1–5379) as query sequences (see Table 32, on CD). A polynucleotide sequence of a stress-regulated gene as disclosed herein can be particularly useful for performing the methods of the invention on a variety of plants, including but not limited to, corn ( Zea mays ), Brassica sp. (e.g., B. napus, B. rapa, B. juncea ), particularly those Brassica species useful as sources of seed oil, alfalfa ( Medicago sativa ), rice ( Oryza sativa ), rye ( Secale cereale ), sorghum ( Sorghum bicolor, Sorghum vulgare ), millet (e.g., pearl millet ( Pennisetum glaucum ), proso millet ( Panicum miliaceum ), foxtail millet ( Setaria italica ), finger millet ( Eleusine coracana )), sunflower ( Helianthus annuus ), safflower ( Carthamus tinctorius ), wheat ( Triticum aestivum ), soybean ( Glycine max ), tobacco ( Nicotiana tabacum ), potato ( Solanum tuberosum ), peanuts ( Arachis hypogaea ), cotton ( Gossypium barbadense, Gossypium hirsutum ), sweet potato ( Ipomoea batatus ), cassava ( Manihot esculenta ), coffee ( Cofea spp.), coconut ( Cocos nucifera ), pineapple ( Ananas comosus ), citrus trees ( Citrus spp.), cocoa ( Theobroma cacao ), tea ( Camellia sinensis ), banana ( Musa spp.), avocado ( Persea ultilane ), fig ( Ficus casica ), guava ( Psidium guajava ), mango ( Mangifera indica ), olive ( Olea europaea ), papaya ( Carica papaya ), cashew ( Anacardium occidentale ), macadamia ( Macadamia integrifolia ), almond ( Prunus amygdalus ), sugar beets ( Beta vulgaris ), sugarcane ( Saccharum spp.), oats, duckweed ( Lemna ), barley, tomatoes ( Lycopersicon esculentum ), lettuce (e.g., Lactuca sativa ), green beans ( Phaseolus vulgaris ), lima beans ( Phaseolus limensis ), peas ( Lathyrus spp.), and members of the genus Cucumis such as cucumber ( C. sativus ), cantaloupe ( C. cantalupensis ), and musk melon ( C. melo ). Ornamentals such as azalea ( Rhododendron spp.), hydrangea ( Macrophylla hydrangea ), hibiscus ( Hibiscus rosasanensis ), roses ( Rosa spp.), tulips ( Tulipa spp.), daffodils ( Narcissus spp.), petunias ( Petunia hybrida ), carnation ( Dianthus caryophyllus ), poinsettia ( Euphorbia pulcherrima ), and chrysanthemum are also included. Additional ornamentals within the scope of the invention include impatiens, Begonia, Pelargonium, Viola, Cyclamen, Verbena, Vinca, Tagetes, Primula, Saint Paulia, Agertum, Amaranthus, Antihirrhinum, Aquilegia, Cineraria, Clover, Cosmo, Cowpea, Dahlia, Datura, Delphinium, Gerbera, Gladiolus, Gloxinia, Hippeastrum, Mesembryanthemum, Salpiglossos, and Zinnia. Conifers that may be employed in practicing the present invention include, for example, pines such as loblolly pine ( Pinus taeda ), slash pine ( Pinus elliotii ), ponderosa pine ( Pinus ponderosa ), lodgepole pine ( Pinus contorta ), and Monterey pine ( Pinus radiata ), Douglas-fir ( Pseudotsuga menziesii ); Western hemlock ( Tsuga ultilane ); Sitka spruce ( Picea glauca ); redwood ( Sequoia sempervirens ); true firs such as silver fir ( Abies amabilis ) and balsam fir ( Abies balsamea ); and cedars such as Western red cedar ( Thuja plicata ) and Alaska yellow-cedar ( Chamaecyparis nootkatensis ). Leguminous plants which may be used in the practice of the present invention include beans and peas. Beans include guar, locust bean, fenugreek, soybean, garden beans, cowpea, mung bean, lima bean, fava bean, lentils, chickpea, etc. Legumes include, but are not limited to, Arachis , e.g., peanuts, Vicia , e.g., crown vetch, hairy vetch, adzuki bean, mung bean, and chickpea, Lupinus , e.g., lupine, trifolium, Phaseolus , e.g., common bean and lima bean, Pisum , e.g., field bean, Melilotus , e.g., clover, Medicago , e.g., alfalfa, Lotus , e.g., trefoil, lens, e.g., lentil, and false indigo. Preferred forage and turf grass for use in the methods of the invention include alfalfa, orchard grass, tall fescue, perennial ryegrass, creeping bent grass, and redtop. Other plants within the scope of the invention include Acacia , aneth, artichoke, arugula, blackberry, canola, cilantro, clementines, escarole, eucalyptus, fennel, grapefruit, honey dew, jicama, kiwifruit, lemon, lime, mushroom, nut, okra, orange, parsley, persimmon, plantain, pomegranate, poplar, radiata pine, radicchio, Southern pine, sweetgum, tangerine, triticale, vine, yams, apple, pear, quince, cherry, apricot, melon, hemp, buckwheat, grape, raspberry, chenopodium, blueberry, nectarine, peach, plum, strawberry, watermelon, eggplant, pepper, cauliflower, Brassica , e.g., broccoli, cabbage, ultilan sprouts, onion, carrot, leek, beet, broad bean, celery, radish, pumpkin, endive, gourd, garlic, snapbean, spinach, squash, turnip, ultilane, chicory, groundnut and zucchini. As used herein, the term “substantially similar”, when used herein with respect to a nucleotide sequence, means a nucleotide sequence corresponding to a reference nucleotide sequence, wherein the corresponding sequence encodes a polypeptide or comprises a regulatory element having substantially the same structure and function as the polypeptide encoded by the reference nucleotide sequence, for example, where only changes in amino acids not affecting the polypeptide function occur. For purposes of the present invention, a reference (or query) sequence is a polynucleotide sequence as set forth in any of SEQ ID NOS:1–2703 or a polypeptide encoded thereby. Desirably, a substantially similar nucleotide sequence encodes the polypeptide encoded by the reference nucleotide sequence. The percentage of identity between the substantially similar nucleotide sequence and the reference nucleotide sequence desirably is at least 60%, more desirably at least 75%, preferably at least 90%, more preferably at least 95%, still more preferably at least 99% and including 100%. A nucleotide sequence is “substantially similar” to reference nucleotide sequence hybridizes to the reference nucleotide sequence in 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50° C. with washing in 2×SSC, 0.1% SDS at 50° C., more desirably in 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50° C. with washing in 1×SSC, 0.1% SDS at 50° C. (stringent conditions), more desirably still in 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50° C. with washing in 0.5×SSC, 0.1% SDS at 50° C. (high stringency), preferably in 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50° C. with washing in 0.1×SSC, 0.1% SDS at 50° C. (very high stringency), more preferably in 7% sodium dodecyl sulfate (SDS), 0.5 M NaPO 4 , 1 mM EDTA at 50° C. with washing in 0.1×SSC, 0.1% SDS at 65° C. (extremely high stringency). In addition, the term “substantially similar,” when used in reference to a polypeptide sequence, means that an amino acid sequence relative to a reference (query) sequence shares at least about 65% amino acid sequence identity, particularly at least about 75% amino acid sequence identity, and preferably at least about 85%, more preferably at least about 90%, and most preferably at least about 95% or greater amino acid sequence identity. Generally, sequences having an E≦10 −8 are considered to be substantially similar to a query sequence. Such sequence identity can take into account conservative amino acid changes that do not substantially affect the function of a polypeptide. As such, homologs or orthologs of the Arabidopsis stress-regulated nucleotide sequences disclosed herein, variants thereof, and polypeptides substantially similar to the polynucleotide sequence of Arabidopsis stress-regulated genes set forth in SEQ ID NOS:1–5379 are encompassed within the present invention and, therefore, useful for practicing the methods of the invention (see, for example, Table 32, which is on the CD-R filed herewith, and incorporated herein by reference). Homology or identity is often measured using sequence analysis software such as the Sequence Analysis Software Package of the Genetics Computer Group (University of Wisconsin Biotechnology Center, 1710 University Avenue, Madison, Wis. 53705). Such software matches similar sequences by assigning degrees of homology to various deletions, substitutions and other modifications. The terms “homology” and “identity,” when used herein in the context of two or more nucleic acids or polypeptide sequences, refer to two or more sequences or subsequences that are the same or have a specified percentage of amino acid residues or of nucleotides that are the same when compared and aligned for maximum correspondence over a comparison window or designated region as measured using any number of sequence comparison algorithms or by manual alignment and visual inspection. For sequence comparison, typically one sequence acts as a reference sequence, to which test sequences are compared. When using a sequence comparison algorithm, test and reference sequences are entered into a computer, subsequence coordinates are designated, if necessary, and sequence algorithm program parameters are designated. Default program parameters can be used, or alternative parameters can be designated. The sequence comparison algorithm then calculates the percent sequence identities for the test sequences relative to the reference sequence, based on the program parameters. The term “comparison window” is used broadly herein to include reference to a segment of any one of the number of contiguous positions, for example, about 20 to 600 positions, for example, amino acid or nucleotide position, usually about 50 to about 200 positions, more usually about 100 to about 150 positions, in which a sequence may be compared to a reference sequence of the same number of contiguous positions after the two sequences are optimally aligned. Methods of alignment of sequence for comparison are well-known in the art. Optimal alignment of sequences for comparison can be conducted, for example, by the local homology algorithm of Smith and Waterman ( Adv. Appl. Math. 2:482, 1981), by the homology alignment algorithm of Needleman and Wunsch ( J. Mol. Biol. 48:443, 1970), by the search for similarity method of Person and Lipman ( Proc. Natl. Acad. Sci., USA 85:2444, 1988), each of which is incorporated herein by reference; by computerized implementations of these algorithms (GAP, BESTFIT, FASTA, and TFASTA in the Wisconsin Genetics Software Package, Genetics Computer Group, 575 Science Dr., Madison, Wis.); or by manual alignment and visual inspection. Other algorithms for determining homology or identity include, for example, in addition to a BLAST program (Basic Local Alignment Search Tool at the National Center for Biological Information), ALIGN, AMAS (Analysis of Multiply Aligned Sequences), AMPS (Protein Multiple Sequence Alignment), ASSET (Aligned Segment Statistical Evaluation Tool), BANDS, BESTSCOR, BIOSCAN (Biological Sequence Comparative Analysis Node), BLIMPS (BLocks IMProved Searcher), FASTA, Intervals & Points, BMB, CLUSTAL V, CLUSTAL W, CONSENSUS, LCONSENSUS, WCONSENSUS, Smith-Waterman algorithm, DARWIN, Las Vegas algorithm, FNAT (Forced Nucleotide Alignment Tool), Framealign, Framesearch, DYNAMIC, FILTER, FSAP (Fristensky Sequence Analysis Package), GAP (Global Alignment Program), GENAL, GIBBS, GenQuest, ISSC (Sensitive Sequence Comparison), LALIGN (Local Sequence Alignment), LCP (Local Content Program), MACAW (Multiple Alignment Construction & Analysis Workbench), MAP (Multiple Alignment Program), MBLKP, MBLKN, PIMA (Pattern-Induced Multi-sequence Alignment), SAGA (Sequence Alignment by Genetic Algorithm) and WHAT-IF. Such alignment programs can also be used to screen genome databases to identify polynucleotide sequences having substantially identical sequences. A number of genome databases are available for comparison. Several databases containing genomic information annotated with some functional information are maintained by different organizations, and are accessible via the internet, for example, at world wide web addresses (url's) “wwwtigr.org/tdb”; “genetics.wisc.edu”; “genome-www.stanford.edu/˜ball”; “hiv-web.lanl.gov”; “ncbi.nlm.nih.gov”; “ebi.ac.uk”; “Pasteur.fr/other/biology”; and “genome.wi.mit.edu”. In particular, the BLAST and BLAST 2.0 algorithms using default parameters are particularly useful for identifying polynucleotide and polypeptides encompassed within the present invention (Altschul et al. ( Nucleic Acids Res. 25:3389–3402, 1977 ; J. Mol. Biol. 215:403–410, 1990, each of which is incorporated herein by reference). Software for performing BLAST analyses is publicly available through the National Center for Biotechnology Information (http://www.ncbi.nlm.nih.gov). This algorithm involves first identifying high scoring sequence pairs (HSPs) by identifying short words of length W in the query sequence, which either match or satisfy some positive-valued threshold score T when aligned with a word of the same length in a database sequence. T is referred to as the neighborhood word score threshold (Altschul et al., supra, 1977, 1990). These initial neighborhood word hits act as seeds for initiating searches to find longer HSPs containing them. The word hits are extended in both directions along each sequence for as far as the cumulative alignment score can be increased. Cumulative scores are calculated using, for nucleotide sequences, the parameters M (reward score for a pair of matching residues; always >0). For amino acid sequences, a scoring matrix is used to calculate the cumulative score. Extension of the word hits in each direction are halted when: the cumulative alignment score falls off by the quantity X from its maximum achieved value; the cumulative score goes to zero or below, due to the accumulation of one or more negative-scoring residue alignments; or the end of either sequence is reached. The BLAST algorithm parameters W, T, and X determine the sensitivity and speed of the alignment. The BLASTN program (for nucleotide sequences) uses as defaults a wordlength (W) of 11, an expectation (E) of 10, M=5, N=4 and a comparison of both strands. For amino acid sequences, the BLASTP program uses as defaults a wordlength of 3, and expectations (E) of 10, and the BLOSUM62 scoring matrix (see Henikoff and Henikoff, Proc. Natl. Acad. Sci., USA 89:10915, 1989) alignments (B) of 50, expectation (E) of 10, M=5, N=4, and a comparison of both strands. The BLAST algorithm also performs a statistical analysis of the similarity between two sequences (see, for example, Karlin and Altschul, Proc. Natl. Acad. Sci. USA 90:5873, 1993, which is incorporated herein by reference). One measure of similarity provided by BLAST algorithm is the smallest sum probability (P(N)), which provides an indication of the probability by which a match between two nucleotide or amino acid sequences would occur by chance. For example, a nucleic acid is considered similar to a references sequence if the smallest sum probability in a comparison of the test nucleic acid to the reference nucleic acid is less than about 0.2, more preferably less than about 0.01, and most preferably less than about 0.001. Significantly, upon identifying polynucleotides that are substantially similar to those of SEQ ID NOS:1–5379, the identified polynucleotides can be used as query sequences in a BLAST search to identify polynucleotides and polypeptides substantially similar thereto. It should be noted that the nucleotide sequences set forth as SEQ ID NOS:1–2703 comprise coding sequences, whereas the nucleotide sequences set forth as SEQ ID NOS:2704–5379 comprise regulatory sequences. In addition, the coding sequences and regulatory sequences are related in that, for example, SEQ ID NO:1 is the coding sequence of a plant cold regulated gene having a 5′ upstream (regulatory) sequence set forth as SEQ ID NO:2704 (see Table 2). Similarly, SEQ ID NO:2705 comprises a regulatory region of SEQ ID NO:2, SEQ ID NO:2706 comprises a regulatory region of SEQ ID NO:3, and so forth as shown in Table 2. As such, reference herein, for example, to a “polynucleotide comprising SEQ ID NO:1” can, unless indicated otherwise, include at least SEQ ID NO:2704. In some cases, the entire coding region of a plant stress regulated gene or the 5′ upstream sequence has not yet been determined (see, for example, SEQ ID NO:43 in Table 3, where “none” indicates that 5′ upstream regulatory sequences have not yet been determined). However, the determination of a complete coding sequence where only a portion is known or of regulatory sequences where a portion of the coding sequence is known can be made using methods as disclosed herein or otherwise known in the art. In one embodiment, protein and nucleic acid sequence homologies are evaluated using the Basic Local Alignment Search Tool (“BLAST”). In particular, five specific BLAST programs are used to perform the following task: (1) BLASTP and BLAST3 compare an amino acid query sequence against a protein sequence database;(2) BLASTN compares a nucleotide query sequence against a nucleotide sequence database;(3) BLASTX compares the six-frame conceptual translation products of a query nucleotide sequence (both strands) against a protein sequence database;(4) TBLASTN compares a query protein sequence against a nucleotide sequence database translated in all six reading frames (both strands); and(5) TBLASTX compares the six-frame translations of a nucleotide query sequence against the six-frame translations of a nucleotide sequence database. The BLAST programs identify homologous sequences by identifying similar segments, which are referred to herein as “high-scoring segment pairs,” between a query amino or nucleic acid sequence and a test sequence which is preferably obtained from a protein or nucleic acid sequence database. High-scoring segment pairs are preferably identified (i.e., aligned) by means of a scoring matrix, many of which are known in the art. Preferably, the scoring matrix used is the BLOSUM62 matrix (Gonnet et al., Science 256:1443–1445, 1992; Henikoff and Henikoff, Proteins 17:49–61, 1993, each of which is incorporated herein by reference). Less preferably, the PAM or PAM250 matrices may also be used (Schwartz and Dayhoff, eds., “Matrices for Detecting Distance Relationships: Atlas of Protein Sequence and Structure” (Washington, National Biomedical Research Foundation 1978)). BLAST programs are accessible through the U.S. National Library of Medicine, for example, on the world wide web at address (url) “ncbi.nlm.nih.gov”. The parameters used with the above algorithms may be adapted depending on the sequence length and degree of homology studied. In some embodiments, the parameters may be the default parameters used by the algorithms in the absence of instructions from the user. The term “substantially similar” also is used in reference to a comparison of expression profiles of nucleotide sequences, wherein a determination that an expression profile characteristic of a stress response is substantially similar to the profile of nucleic acid molecules expressed in a plant cell being examined (“test plant”) is indicative of exposure of the test plant cell to one or a combination of abiotic stress conditions. When used in reference to such a comparison of expression profiles, the term “substantially similar” means that the individual nucleotide sequences in the test plant cell profile are altered in the same manner as the corresponding nucleotide sequences in the expression profile characteristic of the stress response. By way of example, where exposure to saline results in an increased expression of nucleotide sequences A, B and C, and a decreased expression of nucleotide sequences D and E, as indicated by the expression profile characteristic of a saline stress response, a determination that corresponding nucleotide sequences A, B and C in the test plant cell are increased and that nucleotides sequences D and E are decreased is indicative of exposure of the test plant cell to a saline stress condition. It should be recognized that, where, for example, only nucleotide sequences A, B, D and E are examined in the test plant cell, an increase in A and B and a decrease in D and E expression of the test plant cells is considered to be substantially similar to the expression profile characteristic of a saline stress condition and, therefore, is indicative of exposure of the plant cell to a saline stress condition. Similarly, where the levels of expression of the nucleotide sequences examined in a test plant are altered in the same manner, i.e., are increased or are decreased, as that observed in an expression profile characteristic of a particular stress response, the absolute levels of expression may vary, for example, two-fold, five-fold, ten-fold, or the like. Nevertheless, the expression profile of the test plant cell is considered to be substantially similar to the expression profile characteristic of the particular stress response and, therefore, indicative of exposure of the plant cell to the stress condition. As disclosed herein, clusters of stress-regulated genes (and their products), some of which also have been described as having cellular functions such as enzymatic activity or roles as transcription factors, are involved in the response of plant cells to various abiotic stresses (see Tables 29–31; see, also, Tables 1 and 32). As such, the polynucleotide sequences comprising the genes in a cluster likely share common stress-regulated regulatory elements, including, for example, cold-regulated regulatory elements (SEQ ID NOS:2704–3955), salinity-regulated regulatory elements (SEQ ID NOS:4910–5107, and osmotic pressure-regulated regulatory elements (SEQ ID NO:5108–5263), as well as regulatory elements that are responsive to a combination of stress conditions, but not to any of the individual stress conditions, alone (SEQ ID NOS:3956–4909 and 5263–5379). The identification of such clusters of genes thus provides a means to identify the stress-regulated regulatory elements that control the level of expression of these genes. As used herein, the term “plant stress-regulated gene” means a polynucleotide sequence of a plant, the transcription of which is altered in response to exposure to a stress condition, and the regulatory elements linked to such a polynucleotide sequence and involved in the stress response, which can be induction or repression. In general, plant stress gene regulatory elements are contained within a sequence including approximately two kilobases upstream (5′) of the transcription or translation start site and two kilobases downstream (3′) of the transcription or translation termination site. In the absence of an abiotic stress condition, the stress-regulated gene can normally be unexpressed in the cells, can be expressed at a basal level, which is induced to a higher level in response to the stress condition, or can be expressed at a level that is reduced (decreased) in response to the stress condition. The coding region of a plant stress-regulated gene encodes a stress-regulated polypeptide, and also can be the basis for expression of a functional RNA molecule such as an antisense molecule or ribozyme. A stress-regulated polypeptide can have an adaptive effect on a plant, thereby allowing the plant to better tolerate stress conditions; or can have a maladaptive effect, thereby decreasing the ability of the plant to tolerate the stress conditions. The present invention provides an isolated plant stress-regulated regulatory element, which regulates expression of an operatively linked nucleotide sequence in a plant in response a stress condition. As disclosed herein, a plant stress-regulated regulatory element can be isolated from a polynucleotide sequence of a plant stress-regulated gene comprising a nucleotide sequence as set forth in SEQ ID NOS:1–2703, for example any of SEQ ID NOS:2704–5379 (see Table 2). It is recognized that certain of the polynucleotides set forth as SEQ ID NOS:1–5379 previously have been described as being involved in a stress-regulated response in plants, including SEQ ID NOS:156, 229, 233, 558, 573, 606, 625, 635, 787, 813, 1263, 1386, 1391, 1405, 1445, 1484, 1589, 1609, 1634, 1726, 1866, 1918, and 1928 and, therefore, are not encompassed, in whole or in part, within the compositions of the invention, and are encompassed within only certain particular methods of the invention, for example, methods of making a transgenic plant that is resistant to two or more stress conditions, since, even where such a gene was known to be expressed in response to a single stress condition such as cold or saline (e.g., SEQ ID NO:1263), it was not known prior to the present disclosure that any of these genes was responsive to a combination of stress conditions (for example, a combination of cold and osmotic stress for SEQ ID NOS:1726, 1866, 1918, and 1928; or a combination of cold, osmotic and saline stress for SEQ ID NOS:1263, 1386, 1391, 1405, 1445, 1484, 1589, 1609, and 1634). Methods for identifying and isolating the stress-regulated regulatory element from the disclosed polynucleotides, or genomic DNA clones corresponding thereto, are well known in the art. For example, methods of making deletion constructs or linker-scanner constructs can be used to identify nucleotide sequences that are responsive to a stress condition. Generally, such constructs include a reporter gene operatively linked to the sequence to be examined for regulatory activity. By performing such assays, a plant stress-regulated regulatory element can be defined within a sequence of about 500 nucleotides or fewer, generally at least about 200 nucleotides or fewer, particularly about 50 to 100 nucleotides, and more particularly at least about 20 nucleotides or fewer. Preferably the minimal (core) sequence required for regulating a stress response of a plant is identified. The nucleotide sequences of the genes of a cluster also can be examined using a homology search engine such as described herein to identify sequences of conserved identity, particularly in the nucleotide sequence upstream of the transcription start site. Since all of the genes in a cluster as disclosed are induced in response to a particular stress condition or a particular combination of stress conditions, some or all of the nucleotide sequences can share conserved stress-regulated regulatory elements. By performing such a homology search, putative stress-regulated regulatory elements can be identified. The ability of such identified sequences to function as a plant stress-regulated regulatory element can be confirmed, for example, by operatively linking the sequence to a reporter gene and assaying the construct for responsiveness to a stress condition. As used herein, the term “regulatory element” means a nucleotide sequence that, when operatively linked to a coding region of a gene, effects transcription of the coding region such that a ribonucleic acid (RNA) molecule is transcribed from the coding region. A regulatory element generally can increase or decrease the amount of transcription of a nucleotide sequence, for example, a coding sequence, operatively linked to the element with respect to the level at which the nucleotide sequence would be transcribed absent the regulatory element. Regulatory elements are well known in the art and include promoters, enhancers, silencers, inactivated silencer intron sequences, 3′-untranslated or 5′-untranslated sequences of transcribed sequence, for example, a poly-A signal sequence, or other protein or RNA stabilizing elements, or other gene expression control elements known to regulate gene expression or the amount of expression of a gene product. A regulatory element can be isolated from a naturally occurring genomic DNA sequence or can be synthetic, for example, a synthetic promoter. Regulatory elements can be constitutively expressed regulatory element, which maintain gene expression at a relative level of activity (basal level), or can be regulated regulatory elements. Constitutively expressed regulatory elements can be expressed in any cell type, or can be tissue specific, which are expressed only in particular cell types, phase specific, which are expressed only during particular developmental or growth stages of a plant cell, or the like. A regulatory element such as a tissue specific or phase specific regulatory element or an inducible regulatory element useful in constructing a recombinant polynucleotide or in a practicing a method of the invention can be a regulatory element that generally, in nature, is found in a plant genome. However, the regulatory element also can be from an organism other than a plant, including, for example, from a plant virus, an animal virus, or a cell from an animal or other multicellular organism. A regulatory element useful for practicing method of the present is a promoter element. Useful promoters include, but are not limited to, constitutive, inducible, temporally regulated, developmentally regulated, spatially-regulated, chemically regulated, stress-responsive, tissue-specific, viral and synthetic promoters. Promoter sequences are known to be strong or weak. A strong promoter provides for a high level of gene expression, whereas a weak promoter provides for a very low level of gene expression. An inducible promoter is a promoter that provides for the turning on and off of gene expression in response to an exogenously added agent, or to an environmental or developmental stimulus. A bacterial promoter such as the P tac promoter can be induced to varying levels of gene expression depending on the level of isothiopropylgalactoside added to the transformed bacterial cells. An isolated promoter sequence that is a strong promoter for heterologous nucleic acid is advantageous because it provides for a sufficient level of gene expression to allow for easy detection and selection of transformed cells and provides for a high level of gene expression when desired. Within a plant promoter region there are several domains that are necessary for full function of the promoter. The first of these domains lies immediately upstream of the structural gene and forms the “core promoter region” containing consensus sequences, normally 70 base pairs immediately upstream of the gene. The core promoter region contains the characteristic CAAT and TATA boxes plus surrounding sequences, and represents a transcription initiation sequence that defines the transcription start point for the structural gene. The presence of the core promoter region defines a sequence as being a promoter: if the region is absent, the promoter is non-functional. The core promoter region, however, is insufficient to provide full promoter activity. A series of regulatory sequences upstream of the core constitute the remainder of the promoter. These regulatory sequences determine expression level, the spatial and temporal pattern of expression and, for an important subset of promoters, expression under inductive conditions (regulation by external factors such as light, temperature, chemicals, hormones). To define a minimal promoter region, a DNA segment representing the promoter region is removed from the 5′ region of the gene of interest and operably linked to the coding sequence of a marker (reporter) gene by recombinant DNA techniques well known to the art. The reporter gene is operably linked downstream of the promoter, so that transcripts initiating at the promoter proceed through the reporter gene. Reporter genes generally encode proteins which are easily measured, including, but not limited to, chloramphenicol acetyl transferase (CAT), beta-glucuronidase (GUS), green fluorescent protein (GFP), β-galactosidase (β-GAL), and luciferase. The construct containing the reporter gene under the control of the promoter is then introduced into an appropriate cell type by transfection techniques well known to the art. To assay for the reporter protein, cell lysates are prepared and appropriate assays, which are well known in the art, for the reporter protein are performed. For example, if CAT were the reporter gene of choice, the lysates from cells transfected with constructs containing CAT under the control of a promoter under study are mixed with isotopically labeled chloramphenicol and acetyl-coenzyme A (acetyl-CoA). The CAT enzyme transfers the acetyl group from acetyl-CoA to the 2-position or 3-position of chloramphenicol. The reaction is monitored by thin layer chromatography, which separates acetylated chloramphenicol from unreacted material. The reaction products are then visualized by autoradiography. The level of enzyme activity corresponds to the amount of enzyme that was made, which in turn reveals the level of expression from the promoter of interest. This level of expression can be compared to other promoters to determine the relative strength of the promoter under study. In order to be sure that the level of expression is determined by the promoter, rather than by the stability of the mRNA, the level of the reporter mRNA can be measured directly, for example, by northern blot analysis. Once activity is detected, mutational and/or deletional analyses may be employed to determine the minimal region and/or sequences required to initiate transcription. Thus, sequences can be deleted at the 5′ end of the promoter region and/or at the 3′ end of the promoter region, and nucleotide substitutions introduced. These constructs are then introduced to cells and their activity determined. The choice of promoter will vary depending on the temporal and spatial requirements for expression, and also depending on the target species. In some cases, expression in multiple tissues is desirable. While in others, tissue-specific, e.g., leaf-specific, seed-specific, petal-specific, anther-specific, or pith-specific, expression is desirable. Although many promoters from dicotyledons have been shown to be operational in monocotyledons and vice versa, ideally dicotyledonous promoters are selected for expression in dicotyledons, and monocotyledonous promoters for expression in monocotyledons. There is, however, no restriction to the origin or source of a selected promoter. It is sufficient that the promoters are operational in driving the expression of a desired nucleotide sequence in the particular cell. A range of naturally-occurring promoters are known to be operative in plants and have been used to drive the expression of heterologous (both foreign and endogenous) genes and nucleotide sequences in plants: for example, the constitutive 35S cauliflower mosaic virus (CaMV) promoter, the ripening-enhanced tomato polygalacturonase promoter (Bird et al., 1988), the E8 promoter (Diekman and Fischer, 1988) and the fruit specific 2A1 promoter (Pear et al., 1989). Many other promoters, e.g., U2 and U5 snRNA promoters from maize, the promoter from alcohol dehydrogenase, the Z4 promoter from a gene encoding the Z4 22 kD zein protein, the Z10 promoter from a gene encoding a 10 kD zein protein, a Z27 promoter from a gene encoding a 27 kD zein protein, the A20 promoter from the gene encoding a 19 kD zein protein, inducible promoters, such as the light inducible promoter derived from the pea rbcS gene and the actin promoter from rice, e.g., the actin 2 promoter (WO 00/70067); seed specific promoters, such as the phaseolin promoter from beans, may also be used. The nucleotide sequences of the stress-regulated genes of this invention can also be expressed under the regulation of promoters that are chemically regulated. This enables the nucleic acid sequence or encoded polypeptide to be synthesized only when the crop plants are treated with the inducing chemicals. Chemical induction of gene expression is detailed in EP 0 332 104 and U.S. Pat. No. 5,614,395. In some instances it may be desirable to link a constitutive promoter to a polynucleotide comprising a stress regulated gene of the invention. Examples of some constitutive promoters include the rice actin 1 (Wang et al., 1992; U.S. Pat. No. 5,641,876), CaMV 35S (Odell et al., 1985), CaMV 19S (Lawton et al., 1987), nos, Adh, sucrose synthase; and the ubiquitin promoters. In other situations it may be desirable to limit expression of stress-related sequences to specific tissues or stages of development. As used herein, the term “tissue specific or phase specific regulatory element” means a nucleotide sequence that effects transcription in only one or a few cell types, or only during one or a few stages of the life cycle of a plant, for example, only for a period of time during a particular stage of growth, development or differentiation. The terms “tissue specific” and “phase specific” are used together herein in referring to a regulatory element because a single regulatory element can have characteristics of both types of regulatory elements. For example, a regulatory element active only during a particular stage of plant development also can be expressed only in one or a few types of cells in the plant during the particular stage of development. As such, any attempt to classify such regulatory elements as tissue specific or as phase specific can be difficult. Accordingly, unless indicated otherwise, all regulatory elements having the characteristic of a tissue specific regulatory element, or a phase specific regulatory element, or both are considered together for purposes of the present invention. Examples of tissue specific promoters which have been described include the lectin (Vodkin, 1983; Lindstrom et al., 1990) corn alcohol dehydrogenase 1 (Vogel et al., 1989; Dennis et al., 1984), corn light harvesting complex (Simpson, 1986; Bansal et al., 1992), corn heat shock protein (Odell et al., 1985), pea small subunit RuBP carboxylase (Poulsen et al., 1986), Ti plasmid mannopine synthase and Ti plasmid nopaline synthase (Langridge et al., 1989), petunia chalcone isomerase (vanTunen et al., 1988), bean glycine rich protein 1 (Keller et al., 1989), truncated CaMV 35s (Odell et al., 1985), potato patatin (Wenzler et al., 1989), root cell (Yamamoto et al., 1990), maize zein (Reina et al., 1990; Kriz et al., 1987; Wandelt et al., 1989; Langridge et al., 1983; Reina et al., 1990), globulin-1 (Belanger et al., 1991), α-tubulin, cab (Sullivan et al., 1989), PEPCase (Hudspeth & Grula, 1989), R gene complex-associated promoters (Chandler et al., 1989), histone, and chalcone synthase promoters (Franken et al., 1991). Tissue specific enhancers are described by Fromm et al. (1989). Several other tissue-specific regulated genes and/or promoters have been reported in plants, including genes encoding seed storage proteins such as napin, cruciferin, beta-conglycinin, and phaseolin, zein or oil body proteins such as oleosin, genes involved in fatty acid biosynthesis, including acyl carrier protein, stearoyl-ACP desaturase, fatty acid desaturases (fad 2-1), and other genes expressed during embryonic development such as Bce4 (see, for example, EP 255378 and Kridl et al., 1991). Particularly useful for seed-specific expression is the pea vicilin promoter (Czako et al., 1992). (See also U.S. Pat. No. 5,625,136, which is incorporated herein by reference.) Other useful promoters for expression in mature leaves are those that are switched on at the onset of senescence, such as the SAG promoter from Arabidopsis (Gan et al., 1995). A class of fruit-specific promoters expressed at or during antithesis through fruit development, at least until the beginning of ripening, is discussed in U.S. Pat. No. 4,943,674. cDNA clones that are preferentially expressed in cotton fiber have been isolated (John et al., 1992). cDNA clones from tomato displaying differential expression during fruit development have been isolated and characterized (Mansson et al., 1985, Slater et al., 1985). The promoter for polygalacturonase gene is active in fruit ripening. The polygalacturonase gene is described in U.S. Pat. Nos. 4,535,060, 4,769,061, 4,801,590, and 5,107,065, each of which is incorporated herein by reference. Other examples of tissue-specific promoters include those that direct expression in leaf cells following damage to the leaf (for example, from chewing insects), in tubers (for example, patatin gene promoter), and in fiber cells (an example of a developmentally-regulated fiber cell protein is E6 (John et al., 1992). The E6 gene is most active in fiber, although low levels of transcripts are found in leaf, ovule and flower. Additional tissue specific or phase specific regulatory elements include, for example, the AGL8/FRUITFULL regulatory element, which is activated upon floral induction (Hempel et al., Development 124:3845–3853, 1997, which is incorporated herein by reference); root specific regulatory elements such as the regulatory elements from the RCP1 gene and the LRP1 gene (Tsugeki and Fedoroff, Proc. Natl. Acad., USA 96:12941–12946, 1999; Smith and Fedoroff, Plant Cell 7:735–745, 1995, each of which is incorporated herein by reference); flower specific regulatory elements such as the regulatory elements from the LEAFY gene and the APETELA1 gene (Blazquez et al., Development 124:3835–3844, 1997, which is incorporated herein by reference; Hempel et al., supra, 1997); seed specific regulatory elements such as the regulatory element from the oleosin gene (Plant et al., Plant Mol. Biol. 25:193–205, 1994, which is incorporated herein by reference), and dehiscence zone specific regulatory element. Additional tissue specific or phase specific regulatory elements include the Zn13 promoter, which is a pollen specific promoter (Hamilton et al., Plant Mol. Biol. 18:211–218, 1992, which is incorporated herein by reference); the UNUSUAL FLORAL ORGANS (UFO) promoter, which is active in apical shoot meristem; the promoter active in shoot meristems (Atanassova et al., Plant J. 2:291, 1992, which is incorporated herein by reference), the cdc2a promoter and cyc07 promoter (see, for example, Ito et al., Plant Mol. Biol. 24:863, 1994; Martinez et al., Proc. Natl. Acad. Sci., USA 89:7360, 1992; Medford et al., Plant Cell 3:359, 1991; Terada et al., Plant J. 3:241, 1993; Wissenbach et al., Plant J. 4:411, 1993, each of which is incorporated herein by reference); the promoter of the APETELA3 gene, which is active in floral meristems (Jack et al., Cell 76:703, 1994, which is incorporated herein by reference; Hempel et al., supra, 1997); a promoter of an agamous-like (AGL) family member, for example, AGL8, which is active in shoot meristem upon the transition to flowering (Hempel et al., supra, 1997); floral abscission zone promoters; L1-specific promoters; and the like. The tissue-specificity of some “tissue-specific” promoters may not be absolute and may be tested by one skilled in the art using the diphtheria toxin sequence. One can also achieve tissue-specific expression with “leaky” expression by a combination of different tissue-specific promoters (Beals et al., 1997). Other tissue-specific promoters can be isolated by one skilled in the art (see U.S. Pat. No. 5,589,379). Several inducible promoters (“gene switches”) have been reported, many of which are described in the review by Gatz (1996) and Gatz (1997). These include tetracycline repressor system, Lac repressor system, copper inducible systems, salicylate inducible systems (such as the PR1a system), glucocorticoid (Aoyama et al., 1997) and ecdysone inducible systems. Also included are the benzene sulphonamide (U.S. Pat. No. 5,364,780) and alcohol (WO 97/06269 and WO 97/06268) inducible systems and glutathione S-transferase promoters. In some instances it might be desirable to inhibit expression of a native DNA sequence within a plant's tissues to achieve a desired phenotype. In this case, such inhibition might be accomplished with transformation of the plant to comprise a constitutive, tissue-independent promoter operably linked to an antisense nucleotide sequence, such that constitutive expression of the antisense sequence produces an RNA transcript that interferes with translation of the mRNA of the native DNA sequence. Inducible regulatory elements also are useful for purposes of the present invention. As used herein, the term “inducible regulatory element” means a regulatory element that, when exposed to an inducing agent, effects an increased level of transcription of a nucleotide sequence to which it is operatively linked as compared to the level of transcription, if any, in the absence of an inducing agent. Inducible regulatory elements can be those that have no basal or constitutive activity and only effect transcription upon exposure to an inducing agent, or those that effect a basal or constitutive level of transcription, which is increased upon exposure to an inducing agent. Inducible regulatory elements that effect a basal or constitutive level of expression generally are useful in a method or composition of the invention where the induced level of transcription is substantially greater than the basal or constitutive level of expression, for example, at least about two-fold greater, or at least about five-fold greater. Particularly useful inducible regulatory elements do not have a basal or constitutive activity, or increase the level of transcription at least about ten-fold greater than a basal or constitutive level of transcription associated with the regulatory element. Inducible promoters that have been described include the ABA- and turgor-inducible promoters, the promoter of the auxin-binding protein gene (Schwob et al., 1993), the UDP glucose flavonoid glycosyl-transferase gene promoter (Ralston et al., 1988), the MPI proteinase inhibitor promoter (Cordero et al., 1994), and the glyceraldehyde-3-phosphate dehydrogenase gene promoter (Kohler et al., 1995; Quigley et al., 1989; Martinez et al., 1989). The term “inducing agent” is used to refer to a chemical, biological or physical agent or environmental condition that effects transcription from an inducible regulatory element. In response to exposure to an inducing agent, transcription from the inducible regulatory element generally is initiated de novo or is increased above a basal or constitutive level of expression. Such induction can be identified using the methods disclosed herein, including detecting an increased level of RNA transcribed from a nucleotide sequence operatively linked to the regulatory element, increased expression of a polypeptide encoded by the nucleotide sequence, or a phenotype conferred by expression of the encoded polypeptide. An inducing agent useful in a method of the invention is selected based on the particular inducible regulatory element. For example, the inducible regulatory element can be a metallothionein regulatory element, a copper inducible regulatory element or a tetracycline inducible regulatory element, the transcription from which can be effected in response to metal ions, copper or tetracycline, respectively (Furst et al., Cell 55:705–717, 1988; Mett et al., Proc. Natl. Acad. Sci. USA 90:4567–4571, 1993; Gatz et al., Plant J. 2:397–404, 1992; Roder et al., Mol. Gen. Genet. 243:32–38, 1994, each of which is incorporated herein by reference). The inducible regulatory element also can be an ecdysone regulatory element or a glucocorticoid regulatory element, the transcription from which can be effected in response to ecdysone or other steroid (Christopherson et al., Proc. Natl. Acad. Sci., USA 89:6314–6318, 1992; Schena et al., Proc. Natl. Acad. Sci., USA 88:10421–10425, 1991, each of which is incorporated herein by reference). In addition, the regulatory element can be a cold responsive regulatory element or a heat shock regulatory element, the transcription of which can be effected in response to exposure to cold or heat, respectively (Takahashi et al., Plant Physiol. 99:383–390, 1992, which is incorporated herein by reference). Additional regulatory elements useful in the methods or compositions of the invention include, for example, the spinach nitrite reductase gene regulatory element (Back et al., Plant Mol. Biol. 17:9, 1991, which is incorporated herein by reference); a light inducible regulatory element (Feinbaum et al., Mol. Gen. Genet. 226:449, 1991; Lam and Chua, Science 248:471, 1990, each of which is incorporated herein by reference), a plant hormone inducible regulatory element (Yamaguchi-Shinozaki et al., Plant Mol. Biol. 15:905, 1990; Kares et al., Plant Mol. Biol. 15:225, 1990, each of which is incorporated herein by reference), and the like. An inducible regulatory element also can be a plant stress-regulated regulatory element of the invention. In addition to the known stress conditions that specifically induce or repress expression from such elements, the present invention provides methods of identifying agents that mimic a stress condition. Accordingly, such stress mimics are considered inducing or repressing agents with respect to a plant stress-regulated regulatory element. In addition, a recombinant polypeptide comprising a zinc finger domain, which is specific for the regulatory element, and an effector domain, particularly an activator, can be useful as an inducing agent for a plant stress-regulated regulatory element. Furthermore, such a recombinant polypeptide provides the advantage that the effector domain can be a repressor domain, thereby providing a repressing agent, which decreases expression from the regulatory element. In addition, use of such a method of modulating expression of an endogenous plant stress-regulated gene provides the advantage that the polynucleotide encoding the recombinant polypeptide can be introduced into cells of the plant, thus providing a transgenic plant that can be regulated coordinately with the endogenous plant stress-regulated gene upon exposure to a stress condition. A polynucleotide encoding such a recombinant polypeptide can be operatively linked to and expressed from a constitutively active, inducible or tissue specific or phase specific regulatory element. In one embodiment, the promoter may be a gamma zein promoter, an oleosin ole16 promoter, a globulin I promoter, an actin I promoter, an actin c1 promoter, a sucrose synthetase promoter, an INOPS promoter, an EXM5 promoter, a globulin2 promoter, a b-32, ADPG-pyrophosphorylase promoter, an LtpI promoter, an Ltp2 promoter, an oleosin ole17 promoter, an oleosin ole18 promoter, an actin 2 promoter, a pollen-specific protein promoter, a pollen-specific pectate lyase promoter, an anther-specific protein promoter (Huffman), an anther-specific gene RTS2 promoter, a pollen-specific gene promoter, a tapeturn-specific gene promoter, tapeturn-specific gene RAB24 promoter, a anthranilate synthase alpha subunit promoter, an alpha zein promoter, an anthranilate synthase beta subunit promoter, a dihydrodipicolinate synthase promoter, a Thi 1 promoter, an alcohol dehydrogenase promoter, a cab binding protein promoter, an H3C4 promoter, a RUBISCO SS starch branching enzyme promoter, an ACCase promoter, an actin3 promoter, an actin7 promoter, a regulatory protein GF14-12 promoter, a ribosomal protein L9 promoter, a cellulose biosynthetic enzyme promoter, an S-adenosyl-L-homocysteine hydrolase promoter, a superoxide dismutase promoter, a C-kinase receptor promoter, a phosphoglycerate mutase promoter, a root-specific RCc3 mRNA promoter, a glucose-6 phosphate isomerase promoter, a pyrophosphate-fructose 6-phosphate-1-phosphotransferase promoter, an ubiquitin promoter, a beta-ketoacyl-ACP synthase promoter, a 33 kDa photosystem 11 promoter, an oxygen evolving protein promoter, a 69 kDa vacuolar ATPase subunit promoter, a metallothionein-like protein promoter, a glyceraldehyde-3-phosphate dehydrogenase promoter, an ABA- and ripening-inducible-like protein promoter, a phenylalanine ammonia lyase promoter, an adenosine triphosphatase S-adenosyl-L-homocysteine hydrolase promoter, an a-tubulin promoter, a cab promoter, a PEPCase promoter, an R gene promoter, a lectin promoter, a light harvesting complex promoter, a heat shock protein promoter, a chalcone synthase promoter, a zein promoter, a globulin-1 promoter, an ABA promoter, an auxin-binding protein promoter, a UDP glucose flavonoid glycosyl-transferase gene promoter, an NTI promoter, an actin promoter, an opaque 2 promoter, a b70 promoter, an oleosin promoter, a CaMV 35S promoter, a CaMV 19S promoter, a histone promoter, a turgor-inducible promoter, a pea small subunit RuBP carboxylase promoter, a Ti plasmid mannopine synthase promoter, Ti plasmid nopaline synthase promoter, a petunia chalcone isomerase promoter, a bean glycine rich protein I promoter, a CaMV 35S transcript promoter, a potato patatin promoter, or a S-E9 small subunit RuBP carboxylase promoter. In addition to promoters, a variety of 5′ and 3′ transcriptional regulatory sequences are also available for use in the present invention. Transcriptional terminators are responsible for the termination of transcription and correct mRNA polyadenylation. The 3′-untranslated regulatory DNA sequence preferably includes from about 50 to about 1,000, more preferably about 100 to about 1,000, nucleotide base pairs and contains plant transcriptional and translational termination sequences. Appropriate transcriptional terminators and those which are known to function in plants include the CaMV 35S terminator, the tml terminator, the nopaline synthase terminator, the pea rbcS E9 terminator, the terminator for the T7 transcript from the octopine synthase gene of Agrobacterium tumefaciens , and the 3′ end of the protease inhibitor I or II genes from potato or tomato, although other 3′ elements known to those of skill in the art can also be employed. Alternatively, one also could use a gamma coixin, oleosin 3 or other terminator from the genus Coix . Preferred 3′ elements include those from the nopaline synthase gene of Agrobacterium tumefaciens (Bevan et al., 1983), the terminator for the T7 transcript from the octopine synthase gene of Agrobacterium tumefaciens , and the 3′ end of the protease inhibitor I or II genes from potato or tomato. As the DNA sequence between the transcription initiation site and the start of the coding sequence, i.e., the untranslated leader sequence, can influence gene expression, one may also wish to employ a particular leader sequence. Preferred leader sequences are contemplated to include those that include sequences predicted to direct optimum expression of the attached sequence, i.e., to include a preferred consensus leader sequence that may increase or maintain mRNA stability and prevent inappropriate initiation of translation. The choice of such sequences will be known to those of skill in the art in light of the present disclosure. Sequences that are derived from genes that are highly expressed in plants will be most preferred. Other sequences that have been found to enhance gene expression in transgenic plants include intron sequences (e.g., from Adh1, bronze1, actin1, actin2 (WO 00/760067), or the sucrose synthase intron) and viral leader sequences (e.g., from TMV, MCMV and AMV). For example, a number of non-translated leader sequences derived from viruses are known to enhance expression. Specifically, leader sequences from tobacco mosaic virus (TMV), maize chlorotic mottle virus (MCMV), and alfalfa mosaic virus (AMV) have been shown to be effective in enhancing expression (e.g., Gallie et al., 1987; Skuzeski et al., 1990). Other leaders known in the art include but are not limited to picornavirus leaders, for example, EMCV leader (encephalomyocarditis virus 5′ non-coding region; Elroy-Stein et al., 1989); potyvirus leaders, for example, TEV leader (tobacco etch virus); MDMV leader (maize dwarf mosaic virus); human immunoglobulin heavy chain binding protein (BiP) leader, (Macejak et al., 1991); untranslated leader from the coat protein mRNA of AMV (AMV RNA 4; Jobling et al., 1987), TMV (Gallie et al., 1989), and MCMV (Lommel et al., 1991; see also, della Cioppa et al., 1987). Regulatory elements such as Adh intron 1 (Callis et al., 1987), sucrose synthase intron (Vasil et al., 1989) or TMV omega element (Gallie, et al., 1989), may further be included where desired. Examples of enhancers include elements from the CaMV 35S promoter, octopine synthase genes (Ellis et al., 1987), the rice actin I gene, the maize alcohol dehydrogenase gene (Callis et al., 1987), the maize shrunken I gene (Vasil et al., 1989), TMV Omega element (Gallie et al., 1989) and promoters from non-plant eukaryotes (e.g. yeast; Ma et al., 1988). Vectors for use in accordance with the present invention may be constructed to include the ocs enhancer element, which was first identified as a 16 bp palindromic enhancer from the octopine synthase (ocs) gene of ultilane (Ellis et al., 1987), and is present in at least 10 other promoters (Bouchez et al., 1989). The use of an enhancer element, such as the ocs element and particularly multiple copies of the element, will act to increase the level of transcription from adjacent promoters when applied in the context of monocot transformation. The methods of the invention provide genetically modified plant cells, which can contain, for example, a coding region, or peptide portion thereof, of a plant stress-regulated gene operatively linked to a heterologous inducible regulatory element; or a plant stress-regulated regulatory element operatively linked to a heterologous nucleotide sequence encoding a polypeptide of interest. In such a plant, the expression from the inducible regulatory element can be effected by exposing the plant cells to an inducing agent in any of numerous ways depending, for example, on the inducible regulatory element and the inducing agent. For example, where the inducible regulatory element is a cold responsive regulatory element present in the cells of a transgenic plant, the plant can be exposed to cold conditions, which can be produced artificially, for example, by placing the plant in a thermostatically controlled room, or naturally, for example, by planting the plant in an environment characterized, at least in part, by attaining temperatures sufficient to induce transcription from the promoter but not so cold as to kill the plants. By examining the phenotype of such transgenic plants, those plants that ectopically express a gene product that confers increased resistance of the plant to cold can be identified. Similarly, a transgenic plant containing a metallothionein promoter can be exposed to metal ions such as cadmium or copper by watering the plants with a solution containing the inducing metal ions, or can be planted in soil that is contaminated with a level of such metal ions that is toxic to most plants. The phenotype of surviving plants can be observed, those expressing desirable traits can be selected. As used herein, the term “phenotype” refers to a physically detectable characteristic. A phenotype can be identified visually by inspecting the physical appearance of a plant following exposure, for example, to increased osmotic conditions; can be identified using an assay to detecting a product produced due to expression of reporter gene, for example, an RNA molecule, a polypeptide such as an enzyme, or other detectable signal such as disclosed herein; or by using any appropriate tool useful for identifying a phenotype of a plant, for example, a microscope, a fluorescence activated cell sorter, or the like. A transgenic plant containing an inducible regulatory element such as a steroid inducible regulatory element can be exposed to a steroid by watering the plants with a solution containing the steroid. The use of an inducible regulatory element that is induced upon exposure to a chemical or biological inducing agent that can be placed in solution or suspension in an aqueous medium can be particularly useful because the inducing agent can be applied conveniently to a relatively large crop of transgenic plants containing the inducible regulatory element, for example, through a watering system or by spraying the inducing agent over the field. As such, inducible regulatory elements that are responsive to an environmental inducing agent, for example, cold; heat; metal ions or other potentially toxic agents such as a pesticides, which can contaminate a soil; or the like; or inducible regulatory elements that are regulated by inducing agents that conveniently can be applied to plants, can be particularly useful in a method or composition of the invention, and allow the identification and selection of plants that express desirable traits and survive and grow in environments that otherwise would not support growth of the plants. As disclosed herein, the present invention provides plant stress-regulated regulatory elements, which are identified based on the expression of clusters of plant genes in response to stress. As used herein, the term “stress-regulated regulatory element of a plant” or “plant stress-regulated regulatory element” means a nucleotide sequence of a plant genome that can respond to a stress such that expression of a gene product encoded by a gene comprising the regulatory element (a stress-inducible gene) is increased above or decreased below the level of expression of the gene product in the absence of the stress condition. The regulatory element can be any gene regulatory element, including, for example, a promoter, an enhancer, a silencer, or the like. In one embodiment, the plant stress-regulated regulatory element is a plant stress-regulated promoter. For purposes of modulating the responsiveness of a plant to a stress condition, it can be useful to introduce a modified plant stress-regulated regulatory element into a plant. Such a modified regulatory element can have any desirable characteristic, for example, it can be inducible to a greater level than the corresponding wild-type promoter, or it can be inactivated such that, upon exposure to a stress, there is little or no induction of expression of a nucleotide sequence operatively linked to the mutant element. A plant stress-regulated regulatory element can be modified by incorporating random mutations using, for example, in vitro recombination or DNA shuffling (Stemmer et al., Nature 370: 389–391, 1994; U.S. Pat. No. 5,605,793, each of which is incorporated herein by reference). Using such a method, millions of mutant copies of the polynucleotide, for example, stress-regulated regulatory element, can be produced based on the original nucleotide sequence, and variants with improved properties, such as increased inducibility can be recovered. A mutation method such as DNA shuffling encompasses forming a mutagenized double-stranded polynucleotide from a template double-stranded polynucleotide, wherein the template double-stranded polynucleotide has been cleaved into double stranded random fragments of a desired size, and comprises the steps of adding to the resultant population of double-stranded random fragments one or more single or double stranded oligonucleotides, wherein the oligonucleotides comprise an area of identity and an area of heterology to the double stranded template polynucleotide; denaturing the resultant mixture of double stranded random fragments and oligonucleotides into single stranded fragments; incubating the resultant population of single stranded fragments with a polymerase under conditions that result in the annealing of the single stranded fragments at the areas of identity to form pairs of annealed fragments, the areas of identity being sufficient for one member of a pair to prime replication of the other, thereby forming a mutagenized double-stranded polynucleotide; and repeating the second and third steps for at least two further cycles, wherein the resultant mixture in the second step of a further cycle includes the mutagenized double-stranded polynucleotide from the third step of the previous cycle, and the further cycle forms a further mutagenized double-stranded polynucleotide. Preferably, the concentration of a single species of double stranded random fragment in the population of double stranded random fragments is less than 1% by weight of the total DNA. In addition, the template double stranded polynucleotide can comprise at least about 100 species of polynucleotides. The size of the double stranded random fragments can be from about 5 base pairs to 5 kilobase pairs. In a further embodiment, the fourth step of the method comprises repeating the second and the third steps for at least 10 cycles. A plant stress-regulated regulatory element of the invention is useful for expressing a nucleotide sequence operatively linked to the element in a cell, particularly a plant cell. As used herein, the term “expression” refers to the transcription and/or translation of an endogenous gene or a transgene in plants. In the case of an antisense molecule, for example, the term “expression” refers to the transcription of the polynucleotide encoding the antisense molecule. As used herein, the term “operatively linked,” when used in reference to a plant stress-regulated regulatory element, means that the regulatory element is positioned with respect to a second nucleotide sequence such that the regulatory element effects transcription or transcription and translation of the nucleotide sequence in substantially the same manner, but not necessarily to the same extent, as it does when the regulatory element is present in its natural position in a genome. Transcriptional promoters, for example, generally act in a position and orientation dependent manner and usually are positioned at or within about five nucleotides to about fifty nucleotides 5′ (upstream) of the start site of transcription of a gene in nature. In comparison, enhancers and silencers can act in a relatively position or orientation independent manner and, therefore, can be positioned several hundred or thousand nucleotides upstream or downstream from a transcription start site, or in an intron within the coding region of a gene, yet still be operatively linked to a coding region so as to effect transcription. The second nucleotide sequence, i.e., the sequence operatively linked to the plant stress-regulated regulatory element, can be any nucleotide sequence, including, for example, a coding region of a gene or cDNA; a sequence encoding an antisense molecule, an RNAi molecule, ribozyme, triplexing agent (see, for example, Frank-Kamenetskii and Mirkin, Ann. Rev. Biochem. 64:65–95, 1995), or the like; or a sequence that, when transcribed, can be detected in the cell using, for example, by hybridization or amplification, or when translated produces a detectable signal. The term “coding region” is used broadly herein to include a nucleotide sequence of a genomic DNA or a cDNA molecule comprising all or part of a coding region of the coding strand. A coding region can be transcribed from an operatively linked regulatory element, and can be translated into a full length polypeptide or a peptide portion of a polypeptide. It should be recognized that, in a nucleotide sequence comprising a coding region, not all of the nucleotides in the sequence need necessarily encode the polypeptide and, particularly, that a gene transcript can contain one or more introns, which do not encode an amino acid sequence of a polypeptide but, nevertheless, are part of the coding region, particularly the coding strand, of the gene. The present invention also relates to a recombinant polynucleotide, which contains a polynucleotide portion of a plant stress-regulated gene operatively linked to a heterologous nucleotide sequence. As used herein, the term “polynucleotide portion of plant stress-regulated sequence” means a contiguous nucleotide sequence of the plant stress-regulated gene that provides a function. The portion can be any portion of the sequence, particularly a coding sequence, or a sequence encoding a peptide portion of the stress-regulated polypeptide; the stress-regulated regulatory element; a sequence useful as an antisense molecule or triplexing agent; or a sequence useful for disrupting (knocking-out) an endogenous plant stress-regulated gene. A heterologous nucleotide sequence is a nucleotide sequence that is not normally part of the plant stress-regulated gene from which the polynucleotide portion of the plant stress-regulated gene-component of the recombinant polynucleotide is obtained; or, if it is a part of the plant stress-regulated gene from which the polynucleotide portion is obtained, it is an orientation other than it would normally be in, for example, is an antisense sequence, or comprises at least partially discontinuous as compared to the genomic structure, for example, a single exon operatively linked to the regulatory element. In general, where the polynucleotide portion of the plant stress-regulated gene comprises the coding sequence in a recombinant polynucleotide of the invention, the heterologous nucleotide sequence will function as a regulatory element. The regulatory element can be any heterologous regulatory element, including, for example, a constitutively active regulatory element, an inducible regulatory element, or a tissue specific or phase specific regulatory element, as disclosed above. Conversely, where the polynucleotide portion of the plant stress-regulated polynucleotide comprises the stress-regulated regulatory element of a recombinant polynucleotide of the invention, the heterologous nucleotide sequence generally will be a nucleotide sequence that can be transcribed and, if desired, translated. Where the heterologous nucleotide sequence is expressed from a plant stress-regulated regulatory element, it generally confers a desirable phenotype to a plant cell containing the recombinant polynucleotide, or provides a means to identify a plant cell containing the recombinant polynucleotide. It should be recognized that a “desirable” phenotype can be one that decreases the ability of a plant cell to compete where the plant cell, or a plant containing the cell, is an undesired plant cell. Thus, a heterologous nucleotide sequence can allow a plant to grow, for example, under conditions in which it would not normally be able to grow. A heterologous nucleotide sequence can be, or encode, a selectable marker. As used herein, the term “selectable marker” is used herein to refer to a molecule that, when present or expressed in a plant cell, provides a means to identify a plant cell containing the marker. As such, a selectable marker can provide a means for screening a population of plants, or plant cells, to identify those having the marker. A selectable marker also can confer a selective advantage to the plant cell, or a plant containing the cell. The selective advantage can be, for example, the ability to grow in the presence of a negative selective agent such as an antibiotic or herbicide, compared to the growth of plant cells that do not contain the selectable marker. The selective advantage also can be due, for example, to an enhanced or novel capacity to utilize an added compound as a nutrient, growth factor or energy source. A selectable advantage can be conferred, for example, by a single polynucleotide, or its expression product, or to a combination of polynucleotides whose expression in a plant cell gives the cell with a positive selective advantage, a negative selective advantage, or both. Examples of selectable markers include those that confer antimetabolite resistance, for example, dihydrofolate reductase, which confers resistance to methotrexate (Reiss, Plant Physiol . (Life Sci. Adv.) 13:143–149, 1994); neomycin phosphotransferase, which confers resistance to the aminoglycosides neomycin, kanamycin and paromycin (Herrera-Estrella, EMBO J. 2:987–995, 1983) and hygro, which confers resistance to hygromycin (Marsh, Gene 32:481–485, 1984), trpB, which allows cells to utilize indole in place of tryptophan; hisD, which allows cells to utilize histinol in place of histidine (Hartman, Proc. Natl. Acad. Sci., USA 85:8047, 1988); mannose-6-phosphate isomerase which allows cells to utilize mannose (WO 94/20627); ornithine decarboxylase, which confers resistance to the ornithine decarboxylase inhibitor, 2-(difluoromethyl)-DL-ornithine (DFMO; McConlogue, 1987, In: Current Communications in Molecular Biology, Cold Spring Harbor Laboratory ed.); and deaminase from Aspergillus terreus , which confers resistance to Blasticidin S (Tamura, Biosci. Biotechnol. Biochem. 59:2336–2338, 1995). Additional selectable markers include those that confer herbicide resistance, for example, phosphinothricin acetyltransferase gene, which confers resistance to phosphinothricin (White et al., Nucl. Acids Res. 18:1062, 1990; Spencer et al., Theor. Appl. Genet. 79:625–631, 1990), a mutant EPSPV-synthase, which confers glyphosate resistance (Hinchee et al., Bio/Technology 91:915–922, 1998), a mutant acetolactate synthase, which confers imidazolione or sulfonylurea resistance (Lee et al., EMBO J. 7:1241–1248, 1988), a mutant psbA, which confers resistance to atrazine (Smeda et al., Plant Physiol. 103:911–917, 1993), or a mutant protoporphyrinogen oxidase (see U.S. Pat. No. 5,767,373), or other markers conferring resistance to an herbicide such as glufosinate. In addition, markers that facilitate identification of a plant cell containing the polynucleotide encoding the marker include, for example, luciferase (Giacomin, Plant Sci. 116:59–72, 1996; Scikantha, J. Bacteriol. 178:121, 1996), green fluorescent protein (Gerdes, FEBS Lett. 389:44–47, 1996) or fl-glucuronidase (Jefferson, EMBO J. 6:3901–3907, 1997), and numerous others as disclosed herein or otherwise known in the art. Such markers also can be used as reporter molecules. A heterologous nucleotide sequence can encode an antisense molecule, particularly an antisense molecule specific for a nucleotide sequence of a plant stress-regulated gene, for example, the gene from which the regulatory component of the recombinant polynucleotide is derived. Such a recombinant polynucleotide can be useful for reducing the expression of a plant stress-regulated polypeptide in response to a stress condition because the antisense molecule, like the polypeptide, only will be induced upon exposure to the stress. A heterologous nucleotide sequence also can be, or can encode, a ribozyme or a triplexing agent. In addition to being useful as heterologous nucleotide sequences, such molecules also can be used directly in a method of the invention, for example, to modulate the responsiveness of a plant cell to a stress condition. Thus, an antisense molecule, ribozyme, or triplexing agent can be contacted directly with a target cell and, upon uptake by the cell, can effect their antisense, ribozyme or triplexing activity; or can be encoded by a heterologous nucleotide sequence that is expressed in a plant cell from a plant stress-regulated regulatory element, whereupon it can effect its activity. An antisense polynucleotide, ribozyme or triplexing agent is complementary to a target sequence, which can be a DNA or RNA sequence, for example, messenger RNA, and can be a coding sequence, a nucleotide sequence comprising an intron-exon junction, a regulatory sequence such as a Shine-Delgarno-like sequence, or the like. The degree of complementarity is such that the polynucleotide, for example, an antisense polynucleotide, can interact specifically with the target sequence in a cell. Depending on the total length of the antisense or other polynucleotide, one or a few mismatches with respect to the target sequence can be tolerated without losing the specificity of the polynucleotide for its target sequence. Thus, few if any mismatches would be tolerated in an antisense molecule consisting, for example, of twenty nucleotides, whereas several mismatches will not affect the hybridization efficiency of an antisense molecule that is complementary, for example, to the full length of a target mRNA encoding a cellular polypeptide. The number of mismatches that can be tolerated can be estimated, for example, using well known formulas for determining hybridization kinetics (see Sambrook et al., “Molecular Cloning; A Laboratory Manual” 2nd Edition (Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y.; 1989)) or can be determined empirically using methods as disclosed herein or otherwise known in the art, particularly by determining that the presence of the antisense polynucleotide, ribozyme, or triplexing agent in a cell decreases the level of the target sequence or the expression of a polypeptide encoded by the target sequence in the cell. A nucleotide sequence useful as an antisense molecule, a ribozyme or a triplexing agent can inhibit translation or cleave a polynucleotide encoded by plant stress-regulated gene, thereby modulating the responsiveness of a plant cell to a stress condition. An antisense molecule, for example, can bind to an mRNA to form a double stranded molecule that cannot be translated in a cell. Antisense oligonucleotides of at least about 15 to 25 nucleotides are preferred since they are easily synthesized and can hybridize specifically with a target sequence, although longer antisense molecules can be expressed from a recombinant polynucleotide introduced into the target cell. Specific nucleotide sequences useful as antisense molecules can be identified using well known methods, for example, gene walking methods (see, for example, Seimiya et al., J. Biol. Chem. 272:4631–4636 (1997), which is incorporated herein by reference). Where the antisense molecule is contacted directly with a target cell, it can be operatively associated with a chemically reactive group such as iron-linked EDTA, which cleaves a target RNA at the site of hybridization. A triplexing agent, in comparison, can stall transcription (Maher et al., Antisense Res. Devel. 1:227 (1991); Helene, Anticancer Drug Design 6:569 (1991)). A plant stress-regulated regulatory element can be included in an expression cassette. As used herein, the term “expression cassette” refers to a nucleotide sequence that can direct expression of an operatively linked polynucleotide. Thus, a plant stress-regulated regulatory element can constitute an expression cassette, or component thereof. An expression cassette is particularly useful for directing expression of a nucleotide sequence, which can be an endogenous nucleotide sequence or a heterologous nucleotide sequence, in a cell, particularly a plant cell. If desired, an expression cassette also can contain additional regulatory elements, for example, nucleotide sequences required for proper translation of a polynucleotide sequence into a polypeptide. In general, an expression cassette can be introduced into a plant cell such that the plant cell, a plant resulting from the plant cell, seeds obtained from such a plant, or plants produced from such seeds are resistant to a stress condition. Additional regulatory sequences as disclosed above or other desirable sequences such as selectable markers or the like can be incorporated into an expression cassette containing a plant stress-regulated regulatory element (see, for example, WO 99/47552). Examples of suitable markers include dihydrofolate reductase (DHFR) or neomycin resistance for eukaryotic cells and tetracycline or ampicillin resistance for E. coli . Selection markers in plants include bleomycin, gentamycin, glyphosate, hygromycin, kanamycin, methotrexate, phleomycin, phosphinotricin, spectinomycin, streptomycin, sulfonamide and sulfonylureas resistance (see, for example, Maliga et al., Methods in Plant Molecular Biology , Cold Spring Harbor Laboratory Press, 1995, page 39). The selection marker can have its own promoter or its expression can be driven by the promoter operably linked to the sequence of interest. Additional sequences such as intron sequences (e.g. from Adh1 or bronze1) or viral leader sequences (e.g. from TMV, MCMV and AIVIV), all of which can enhance expression, can be included in the cassette. In addition, where it is desirable to target expression of a nucleotide sequence operatively linked to the stress-regulated regulatory element, a sequence encoding a cellular localization motif can be included in the cassette, for example, such that an encoded transcript or translation product is translocated to and localizes in the cytosol, nucleus, a chloroplast, or another subcellular organelle. Examples of useful transit peptides and transit peptide sequences can be found in Von Heijne et al., Plant Mol. Biol. Rep. 9: 104, 1991; Clark et al., J. Biol. Chem. 264:17544, 1989; della Cioppa et al., Plant Physiol. 84:965, 1987; Romer et al., Biochem. Biophys. Res. Comm. 196:1414, 1993; Shah et al., Science 233:478, 1986; Archer et al., J. Bioenerg Biomemb. 22:789, 1990; Scandalios, Prog. Clin. Biol. Res. 344:515, 1990; Weisbeek et al., J. Cell Sci. Suppl. 11: 199, 1989; Bruce, Trends Cell Biol. 10:440, 2000. The present invention can utilize native or heterologous transit peptides. The encoding sequence for a transit peptide can include all or a portion of the encoding sequence for a particular transit peptide, and may also contain portions of the mature protein encoding sequence associated with a particular transit peptide. A polynucleotide portion of a plant stress-regulated plant gene, or an expression cassette, can be introduced into a cell as a naked DNA molecule, can be incorporated in a matrix such as a liposome or a particle such as a viral particle, or can be incorporated into a vector. Such vectors can be cloning or expression vectors, but other uses are within the scope of the present invention. A cloning vector is a self-replicating DNA molecule that serves to transfer a DNA segment into a host cell. The three most common types of cloning vectors are bacterial plasmids, phages, and other viruses. An expression vector is a cloning vector designed so that a coding sequence inserted at a particular site will be transcribed and translated into a protein. Incorporation of the polynucleotide into a vector can facilitate manipulation of the polynucleotide, or introduction of the polynucleotide into a plant cell. A vector can be derived from a plasmid or a viral vector such as a T-DNA vector (Horsch et al., Science 227:1229–1231, 1985, which is incorporated herein by reference). If desired, the vector can comprise components of a plant transposable element, for example, a Ds transposon (Bancroft and Dean, Genetics 134:1221–1229, 1993, which is incorporated herein by reference) or an Spm transposon (Aarts et al., Mol. Gen. Genet. 247:555–564, 1995, which is incorporated herein by reference). In addition to containing the polynucleotide portion of a plant stress-regulated gene, a vector can contain various nucleotide sequences that facilitate, for example, rescue of the vector from a transformed plant cell; passage of the vector in a host cell, which can be a plant, animal, bacterial, or insect host cell; or expression of an encoding nucleotide sequence in the vector, including all or a portion of a rescued coding region. As such, the vector can contain any of a number of additional transcription and translation elements, including constitutive and inducible promoters, enhancers, and the like (see, for example, Bitter et al., Meth. Enzymol. 153:516–544, 1987). For example, a vector can contain elements useful for passage, growth or expression in a bacterial system, including a bacterial origin of replication; a promoter, which can be an inducible promoter; and the like. In comparison, a vector that can be passaged in a mammalian host cell system can have a promoter such as a metallothionein promoter, which has characteristics of both a constitutive promoter and an inducible promoter, or a viral promoter such as a retrovirus long terminal repeat, an adenovirus late promoter, or the like. A vector also can contain one or more restriction endonuclease recognition and cleavage sites, including, for example, a polylinker sequence, to facilitate rescue of a nucleotide sequence operably linked to the polynucleotide portion. The present invention also relates to a method of using a polynucleotide portion of a plant stress-regulated gene to confer a selective advantage on a plant cell. Such a method can be performed by introducing, for example, a plant stress-regulated regulatory element into a plant cell, wherein, upon exposure of the plant cell to a stress condition to which the regulatory element is responsive, a nucleotide sequence operatively linked to the regulatory element is expressed, thereby conferring a selective advantage to plant cell. The operatively linked nucleotide sequence can be a heterologous nucleotide sequence, which can be operatively linked to the regulatory element prior to introduction of the regulatory sequence into the plant cell; or can be an endogenous nucleotide sequence into which the regulatory element was targeted by a method such as homologous recombination. The selective advantage conferred by the operatively linked nucleotide sequence can be such that the plant is better able to tolerate the stress condition; or can be any other selective advantage. As used herein, the term “selective advantage” refers to the ability of a particular organism to better propagate, develop, grow, survive, or otherwise tolerate a condition as compared to a corresponding reference organism that does not contain a plant-stress regulated polynucleotide portion of the present invention. In one embodiment, a selective advantage is exemplified by the ability of a desired plant, plant cell, or the like, that contains an introduced plant stress-regulated regulatory element, to grow better than an undesired plant, plant cell, or the like, that does not contain the introduced regulatory element. For example, a recombinant polynucleotide comprising a plant stress-regulated regulatory element operatively linked to a heterologous nucleotide sequence encoding an enzyme that inactivates an herbicide can be introduced in a desired plant. Upon exposure of a mixed population of plants comprising the desired plants, which contain the recombinant polynucleotide, and one or more other populations of undesired plants, which lack the recombinant polynucleotide, to a stress condition that induces expression of the regulatory element and to the herbicide, the desired plants will have a greater likelihood of surviving exposure to the toxin and, therefore, a selective advantage over the undesired plants. In another embodiment, a selective advantage is exemplified by the ability of a desired plant, plant cell, or the like, to better propagate, develop, grow, survive, or otherwise tolerate a condition as compared to an undesired plant, plant cell, or the like, that contains an introduced plant stress-regulated regulatory element. For example, a recombinant polynucleotide comprising a plant stress-regulated regulatory element operatively linked to a plant cell toxin can be introduced into cells of an undesirable plant present in a mixed population of desired and undesired plants, for example, food crops and weeds, respectively, then the plants can be exposed to stress conditions that induce expression from the plant stress-regulated regulatory element, whereby expression of the plant cell toxin results in inhibition of growth or death of the undesired plants, thereby providing a selective advantage to the desired plants, which no longer have to compete with the undesired plants for nutrients, light, or the like. In another example, a plant stress-regulated regulatory element operatively linked to a plant cell toxin can be introduced into cells of plants used as a nurse crop. Nurse crops, also called cover or companion crops, are planted in combination with plants of interest to provide, among other things, shade and soil stability during establishment of the desired plants. Once the desired plants have become established, the presence of the nurse crop may no longer be desirable. Exposure to conditions inducing expression of the gene linked to the plant stress-regulated regulatory element allows elimination of the nurse crop. Alternatively nurse crops can be made less tolerate to abiotic stress by the inhibition of any of the stress-regulated sequences disclosed herein. Inhibition can be accomplished by any of the method described herein. Upon exposure of the nurse crop to the stress, the decreased ability of the nurse crop to respond to the stress will result in elimination of the nurse crop, leaving only the desired plants. The invention also provides a means of producing a transgenic plant, which comprises plant cells that exhibit altered responsiveness to a stress condition. As such, the present invention further provides a transgenic plant, or plant cells or tissues derived therefrom, which are genetically modified to respond to stress differently than a corresponding wild-type plant or plant not containing constructs of the present invention would respond. As used herein, the term “responsiveness to a stress condition” refers to the ability of a plant to express a plant stress-regulated gene upon exposure to the stress condition. A transgenic plant cell contains a polypeptide portion of a plant stress-regulated gene, or a mutant form thereof, for example, a knock-out mutant. A knock-out mutant form of a plant stress-regulated gene can contain, for example, a mutation such that a STOP codon is introduced into the reading frame of the translated portion of the gene such that expression of a functional stress-regulated polypeptide is prevented; or a mutation in the stress-regulated regulatory element such that inducibility of the element in response to a stress condition is inhibited. Such transgenic plants of the invention can display any of various idiotypic modifications is response to an abiotic stress, including altered tolerance to the stress condition, as well as increased or decreased plant growth, root growth, yield, or the like, as compared to the corresponding wild-type plant. The term “plant” is used broadly herein to include any plant at any stage of development, or to part of a plant, including a plant cutting, a plant cell, a plant cell culture, a plant organ, a plant seed, and a plantlet. A plant cell is the structural and physiological unit of the plant, comprising a protoplast and a cell wall. A plant cell can be in the form of an isolated single cell or a cultured cell, or can be part of higher organized unit, for example, a plant tissue, plant organ, or plant. Thus, a plant cell can be a protoplast, a gamete producing cell, or a cell or collection of cells that can regenerate into a whole plant. As such, a seed, which comprises multiple plant cells and is capable of regenerating into a whole plant, is considered plant cell for purposes of this disclosure. A plant tissue or plant organ can be a seed, protoplast, callus, or any other groups of plant cells that is organized into a structural or functional unit. Particularly useful parts of a plant include harvestable parts and parts useful for propagation of progeny plants. A harvestable part of a plant can be any useful part of a plant, for example, flowers, pollen, seedlings, tubers, leaves, stems, fruit, seeds, roots, and the like. A part of a plant useful for propagation includes, for example, seeds, fruits, cuttings, seedlings, tubers, rootstocks, and the like. A transgenic plant can be regenerated from a transformed plant cell. As used herein, the term “regenerate” means growing a whole plant from a plant cell; a group of plant cells; a protoplast; a seed; or a piece of a plant such as a callus or tissue. Regeneration from protoplasts varies from species to species of plants. For example, a suspension of protoplasts can be made and, in certain species, embryo formation can be induced from the protoplast suspension, to the stage of ripening and germination. The culture media generally contains various components necessary for growth and regeneration, including, for example, hormones such as auxins and cytokinins; and amino acids such as glutamic acid and proline, depending on the particular plant species. Efficient regeneration will depend, in part, on the medium, the genotype, and the history of the culture. If these variables are controlled, however, regeneration is reproducible. Regeneration can occur from plant callus, explants, organs or plant parts. Transformation can be performed in the context of organ or plant part regeneration. (see Meth. Enzymol . Vol. 118; Klee et al. Ann. Rev. Plant Physiol. 38:467, 1987, which is incorporated herein by reference). Utilizing the leaf disk-transformation-regeneration method, for example, disks are cultured on selective media, followed by shoot formation in about two to four weeks (see Horsch et al., supra, 1985). Shoots that develop are excised from calli and transplanted to appropriate root-inducing selective medium. Rooted plantlets are transplanted to soil as soon as possible after roots appear. The plantlets can be repotted as required, until reaching maturity. In vegetatively propagated crops, the mature transgenic plants are propagated utilizing cuttings or tissue culture techniques to produce multiple identical plants. Selection of desirable transgenotes is made and new varieties are obtained and propagated vegetatively for commercial use. In seed propagated crops, the mature transgenic plants can be self crossed to produce a homozygous inbred plant. The resulting inbred plant produces seeds that contain the introduced plant stress-induced regulatory element, and can be grown to produce plants that express a polynucleotide or polypeptide in response to a stress condition that induces expression from the regulatory element. As such, the invention further provides seeds produced by a transgenic plant obtained by a method of the invention. In addition, transgenic plants comprising different recombinant sequences can be crossbred, thereby providing a means to obtain transgenic plants containing two or more different transgenes, each of which contributes a desirable characteristic to the plant. Methods for breeding plants and selecting for crossbred plants having desirable characteristics or other characteristics of interest are well known in the art. A method of the invention can be performed by introducing a polynucleotide portion of a plant stress-regulated gene into the plant. As used herein, the term “introducing” means transferring a polynucleotide into a plant cell. A polynucleotide can be introduced into a cell by a variety of methods well known to those of ordinary skill in the art. For example, the polynucleotide can be introduced into a plant cell using a direct gene transfer method such as electroporation or microprojectile mediated transformation, or using Agrobacterium mediated transformation. Non-limiting examples of methods for the introduction of polynucleotides into plants are provided in greater detail herein. As used herein, the term “transformed” refers to a plant cell containing an exogenously introduced polynucleotide portion of a plant stress-regulated gene that is or can be rendered active in a plant cell, or to a plant comprising a plant cell containing such a polynucleotide. It should be recognized that one or more polynucleotides, which are the same or different can be introduced into a plant, thereby providing a means to obtain a genetically modified plant containing multiple copies of a single transgenic sequence, or containing two or more different transgenic sequences, either or both of which can be present in multiple copies. Such transgenic plants can be produced, for example, by simply selecting plants having multiple copies of a single type of transgenic sequence; by cotransfecting plant cells with two or more populations of different transgenic sequences and identifying those containing the two or more different transgenic sequences; or by crossbreeding transgenic plants, each of which contains one or more desired transgenic sequences, and identifying those progeny having the desired sequences. Methods for introducing a polynucleotide into a plant cell to obtain a transformed plant also include direct gene transfer (see European Patent A 164 575), injection, electroporation, biolistic methods such as particle bombardment, pollen-mediated transformation, plant RNA virus-mediated transformation, liposome-mediated transformation, transformation using wounded or enzyme-degraded immature embryos, or wounded or enzyme-degraded embryogenic callus, and the like. Transformation methods using Agrobacterium tumefaciens tumor inducing (Ti) plasmids or root-inducing (Ri) plasmids, or plant virus vectors are well known in the art (see, for example, WO 99/47552; Weissbach & Weissbach, “Methods for Plant Molecular Biology” (Academic Press, NY 1988), section VIII, pages 421–463; Grierson and Corey, “Plant Molecular Bioloy” 2d Ed. (Blackie, London 1988), Chapters 7–9, each of which is incorporated herein by reference; Horsch et al., supra, 1985). The wild-type form of Agrobacterium , for example, contains a Ti plasmid, which directs production of tumorigenic crown gall growth on host plants. Transfer of the tumor inducing T-DNA region of the Ti plasmid to a plant genome requires the Ti plasmid-encoded virulence genes as well as T-DNA borders, which are a set of direct DNA repeats that delineate the region to be transferred. An Agrobacterium based vector is a modified form of a Ti plasmid, in which the tumor inducing functions are replaced by a nucleotide sequence of interest that is to be introduced into the plant host. Methods of using Agrobacterium mediated transformation include cocultivation of Agrobacterium with cultured isolated protoplasts; transformation of plant cells or tissues with Agrobacterium ; and transformation of seeds, apices or meristems with Agrobacterium . In addition, in planta transformation by Agrobacterium can be performed using vacuum infiltration of a suspension of Agrobacterium cells (Bechtold et al., C. R. Acad. Sci. Paris 316:1194, 1993, which is incorporated herein by reference). Agrobacterium mediated transformation can employ cointegrate vectors or binary vector systems, in which the components of the Ti plasmid are divided between a helper vector, which resides permanently in the Agrobacterium host and carries the virulence genes, and a shuttle vector, which contains the gene of interest bounded by T-DNA sequences. Binary vectors are well known in the art (see, for example, De Framond, BioTechnology 1:262, 1983; Hoekema et al., Nature 303:179, 1983, each of which is incorporated herein by reference) and are commercially available (Clontech; Palo Alto Calif.). For transformation, Agrobacterium can be cocultured, for example, with plant cells or wounded tissue such as leaf tissue, root explants, hypocotyledons, stem pieces or tubers (see, for example, Glick and Thompson, “Methods in Plant Molecular Biology and Biotechnology” (Boca Raton Fla., CRC Press 1993), which is incorporated herein by reference). Wounded cells within the plant tissue that have been infected by Agrobacterium can develop organs de novo when cultured under the appropriate conditions; the resulting transgenic shoots eventually give rise to transgenic plants, which contain an exogenous polynucleotide portion of a plant stress-regulated gene. Agrobacterium mediated transformation has been used to produce a variety of transgenic plants, including, for example, transgenic cruciferous plants such as Arabidopsis , mustard, rapeseed and flax; transgenic leguminous plants such as alfalfa, pea, soybean, trefoil and white clover; and transgenic solanaceous plants such as eggplant, petunia, potato, tobacco and tomato (see, for example, Wang et al., “Transformation of Plants and Soil Microorganisms” (Cambridge, University Press 1995), which is incorporated herein by reference). In addition, Agrobacterium mediated transformation can be used to introduce an exogenous polynucleotide sequence, for example, a plant stress-regulated regulatory element into apple, aspen, belladonna, black currant, carrot, celery, cotton, cucumber, grape, horseradish, lettuce, morning glory, muskmelon, neem, poplar, strawberry, sugar beet, sunflower, walnut, asparagus, rice and other plants (see, for example, Glick and Thompson, supra, 1993; Hiei et al., Plant J. 6:271–282, 1994; Shimamoto, Science 270:1772–1773, 1995). Suitable strains of Agrobacterium tumefaciens and vectors as well as transformation of Agrobacteria and appropriate growth and selection media are well known in the art (GV3101, pMK90RK), Koncz, Mol. Gen. Genet. 204:383–396, 1986; (C58C1, pGV3850kan), Deblaere, Nucl. Acid Res. 13:4777, 1985; Bevan, Nucl. Acid Res. 12:8711, 1984; Koncz, Proc. Natl. Acad. Sci. USA 86:8467–8471, 1986; Koncz, Plant Mol. Biol. 20:963–976, 1992; Koncz, Specialized vectors for gene tagging and expression studies. In: Plant Molecular Biology Manual Vol. 2, Gelvin and Schilperoort (Eds.), Dordrecht, The Netherlands: Kluwer Academic Publ. (1994), 1–22; European Patent A-1 20 516; Hoekema: The Binary Plant Vector System, Offsetdrukkerij Kanters B. V., Alblasserdam (1985), Chapter V; Fraley, Crit. Rev. Plant. Sci., 4:1–46; An, EMBO J. 4:277–287, 1985). Where a polynucleotide portion of a plant stress-regulated gene is contained in vector, the vector can contain functional elements, for example “left border” and “right border” sequences of the T-DNA of Agrobacterium , which allow for stable integration into a plant genome. Furthermore, methods and vectors that permit the generation of marker-free transgenic plants, for example, where a selectable marker gene is lost at a certain stage of plant development or plant breeding, are known, and include, for example, methods of co-transformation (Lyznik, Plant Mol. Biol. 13:151–161, 1989; Peng, Plant Mol. Biol. 27:91–104, 1995), or methods that utilize enzymes capable of promoting homologous recombination in plants (see, e.g., WO97/08331; Bayley, Plant Mol. Biol. 18:353–361, 1992; Lloyd, Mol. Gen. Genet. 242:653–657, 1994; Maeser, Mol. Gen. Genet. 230:170–176, 1991; Onouchi, Nucl. Acids Res. 19:6373–6378, 1991; see, also, Sambrook et al., supra, 1989). A direct gene transfer method such as electroporation also can be used to introduce a polynucleotide portion of a plant stress-regulated gene into a cell such as a plant cell. For example, plant protoplasts can be electroporated in the presence of the regulatory element, which can be in a vector (Fromm et al., Proc. Natl. Acad. Sci., USA 82:5824, 1985, which is incorporated herein by reference). Electrical impulses of high field strength reversibly permeabilize membranes allowing the introduction of the nucleic acid. Electroporated plant protoplasts reform the cell wall, divide and form a plant callus. Microinjection can be performed as described in Potrykus and Spangenberg (eds.), Gene Transfer To Plants (Springer Verlag, Berlin, N.Y. 1995). A transformed plant cell containing the introduced polynucleotide can be identified by detecting a phenotype due to the introduced polynucleotide, for example, increased or decreased tolerance to a stress condition. Microprojectile mediated transformation also can be used to introduce a polynucleotide into a plant cell (Klein et al., Nature 327:70–73, 1987, which is incorporated herein by reference). This method utilizes microprojectiles such as gold or tungsten, which are coated with the desired nucleic acid molecule by precipitation with calcium chloride, spermidine or polyethylene glycol. The microprojectile particles are accelerated at high speed into a plant tissue using a device such as the BIOLISTIC PD-1000 (BioRad; Hercules Calif.). Microprojectile mediated delivery (“particle bombardment”) is especially useful to transform plant cells that are difficult to transform or regenerate using other methods. Methods for the transformation using biolistic methods are well known (Wan, Plant Physiol. 104:37–48, 1984; Vasil, Bio/Technology 11:1553–1558, 1993; Christou, Trends in Plant Science 1:423–431, 1996). Microprojectile mediated transformation has been used, for example, to generate a variety of transgenic plant species, including cotton, tobacco, corn, hybrid poplar and papaya (see Glick and Thompson, supra, 1993). Important cereal crops such as wheat, oat, barley, sorghum and rice also have been transformed using microprojectile mediated delivery (Duan et al., Nature Biotech. 14:494–498, 1996; Shimamoto, Curr. Opin. Biotech. 5:158–162, 1994). A rapid transformation regeneration system for the production of transgenic plants such as a system that produces transgenic wheat in two to three months (see European Patent No. EP 0709462A2, which is incorporated herein by reference) also can be useful for producing a transgenic plant using a method of the invention, thus allowing more rapid identification of gene functions. The transformation of most dicotyledonous plants is possible with the methods described above. Transformation of monocotyledonous plants also can be transformed using, for example, biolistic methods as described above, protoplast transformation, electroporation of partially permeabilized cells, introduction of DNA using glass fibers, Agrobacterium mediated transformation, and the like. Plastid transformation also can be used to introduce a polynucleotide portion of a plant stress-regulated gene into a plant cell (U.S. Pat. Nos. 5,451,513, 5,545,817, and 5,545,818; WO 95/16783; McBride et al., Proc. Natl. Acad. Sci., USA 91:7301–7305, 1994). Chloroplast transformation involves introducing regions of cloned plastid DNA flanking a desired nucleotide sequence, for example, a selectable marker together with polynucleotide of interest into a suitable target tissue, using, for example, a biolistic or protoplast transformation method (e.g., calcium chloride or PEG mediated transformation). One to 1.5 kb flanking regions (“targeting sequences”) facilitate homologous recombination with the plastid genome, and allow the replacement or modification of specific regions of the plastome. Using this method, point mutations in the chloroplast 16S rRNA and rps12 genes, which confer resistance to spectinomycin and streptomycin, can be utilized as selectable markers for transformation (Svab et al., Proc. Natl. Acad. Sci., USA 87:8526–8530, 1990; Staub and Maliga, Plant Cell 4:39–45, 1992), resulted in stable homopiasmic transformants; at a frequency of approximately one per 100 bombardments of target leaves. The presence of cloning sites between these markers allowed creation of a plastid targeting vector for introduction of foreign genes (Staub and Maliga, EMBO J. 12:601–606, 1993). Substantial increases in transformation frequency are obtained by replacement of the recessive rRNA or r-protein antibiotic resistance genes with a dominant selectable marker, the bacterial aadA gene encoding the spectinomycin-detoxifying enzyme aminoglycoside-3′-adenyltransferase (Svab and Maliga, Proc. Natl. Acad. Sci., USA 90:913–917, 1993). Approximately 15 to 20 cell division cycles following transformation are generally required to reach a homoplastidic state. Plastid expression, in which genes are inserted by homologous recombination into all of the several thousand copies of the circular plastid genome present in each plant cell, takes advantage of the enormous copy number advantage over nuclear-expressed genes to permit expression levels that can readily exceed 10% of the total soluble plant protein. Plants suitable to treatment according to a method of the invention can be monocots or dicots and include, but are not limited to, corn ( Zea mays ), Brassica sp. (e.g., B. napus, B. rapa, B. juncea ), particularly those Brassica species useful as sources of seed oil, alfalfa ( Medicago sativa ), rice ( Oryza sativa ), rye ( Secale cereale ), sorghum ( Sorghum bicolor, Sorghum vulgare ), millet (e.g., pearl millet ( Pennisetum glaucum ), proso millet ( Panicum miliaceum ), foxtail millet ( Setaria italica ), finger millet ( Eleusine coracana )), sunflower ( Helianthus annuus ), safflower ( Carthamus tinctorius ), wheat ( Triticum aestivum ), soybean ( Glycine max ), tobacco ( Nicotiana tabacum ), potato ( Solanum tuberosum ), peanuts ( Arachis hypogaea ), cotton ( Gossypium barbadense, Gossypium hirsutum ), sweet potato ( Ipomoea batatus ), cassava ( Manihot esculenta ), coffee ( Cofea spp.), coconut ( Cocos nucifera ), pineapple ( Ananas comosus ), citrus trees ( Citrus spp.), cocoa ( Theobroma cacao ), tea ( Camellia sinensis ), banana ( Musa spp.), avocado ( Persea ultilane ), fig ( Ficus casica ), guava ( Psidium guajava ), mango ( Mangifera indica ), olive ( Olea europaea ), papaya ( Carica papaya ), cashew ( Anacardium occidentale ), macadamia ( Macadamia integrifolia ), almond ( Prunus amygdalus ), sugar beets ( Beta vulgaris ), sugarcane ( Saccharum spp.), oats, duckweed ( Lemna ), barley, tomatoes ( Lycopersicon esculentum ), lettuce (e.g., Lactuca sativa ), green beans ( Phaseolus vulgaris ), lima beans ( Phaseolus limensis ), peas ( Lathyrus spp.), and members of the genus Cucumis such as cucumber ( C. sativus ), cantaloupe ( C. cantalupensis ), and musk melon ( C. melo ). Ornamentals such as azalea ( Rhododendron spp.), hydrangea ( Macrophylla hydrangea ), hibiscus ( Hibiscus rosasanensis ), roses ( Rosa spp.), tulips ( Tulipa spp.), daffodils ( Narcissus spp.), petunias ( Petunia hybrida ), carnation ( Dianthus caryophyllus ), poinsettia ( Euphorbia pulcherrima ), and chrysanthemum are also included. Additional ornamentals within the scope of the invention include impatiens, Begonia, Pelargonium, Viola, Cyclamen, Verbena, Vinca, Tagetes, Primula, Saint Paulia, Agertum, Amaranthus, Antihirrhinum, Aquilegia, Cineraria, Clover, Cosmo, Cowpea, Dahlia, Datura, Delphinium, Gerbera, Gladiolus, Gloxinia, Hippeastrum, Mesembryanthemum, Salpiglossos, and Zinnia. Conifers that may be employed in practicing the present invention include, for example, pines such as loblolly pine ( Pinus taeda ), slash pine ( Pinus elliotii ), ponderosa pine ( Pinus ponderosa ), lodgepole pine ( Pinus contorta ), and Monterey pine ( Pinus radiata ), Douglas-fir ( Pseudotsuga menziesii ); Western hemlock ( Tsuga ultilane ); Sitka spruce ( Picea glauca ); redwood ( Sequoia sempervirens ); true firs such as silver fir ( Abies amabilis ) and balsam fir ( Abies balsamea ); and cedars such as Western red cedar ( Thuja plicata ) and Alaska yellow-cedar ( Chamaecyparis nootkatensis ). Leguminous plants which may be used in the practice of the present invention include beans and peas. Beans include guar, locust bean, fenugreek, soybean, garden beans, cowpea, mungbean, lima bean, fava bean, lentils, chickpea, etc. Legumes include, but are not limited to, Arachis , e.g., peanuts, Vicia , e.g., crown vetch, hairy vetch, adzuki bean, mung bean, and chickpea, Lupinus , e.g., lupine, trifolium, Phaseolus , e.g., common bean and lima bean, Pisum , e.g., field bean, Melilotus , e.g., clover, Medicago , e.g., alfalfa, Lotus , e.g., trefoil, lens, e.g., lentil, and false indigo. Preferred forage and turf grass for use in the methods of the invention include alfalfa, orchard grass, tall fescue, perennial ryegrass, creeping bent grass, and redtop. Other plants within the scope of the invention include Acacia , aneth, artichoke, arugula, blackberry, canola, cilantro, clementines, escarole, eucalyptus, fennel, grapefruit, honey dew, jicama, kiwifruit, lemon, lime, mushroom, nut, okra, orange, parsley, persimmon, plantain, pomegranate, poplar, radiata pine, radicchio, Southern pine, sweetgum, tangerine, triticale, vine, yams, apple, pear, quince, cherry, apricot, melon, hemp, buckwheat, grape, raspberry, chenopodium, blueberry, nectarine, peach, plum, strawberry, watermelon, eggplant, pepper, cauliflower, Brassica , e.g., broccoli, cabbage, ultilan sprouts, onion, carrot, leek, beet, broad bean, celery, radish, pumpkin, endive, gourd, garlic, snapbean, spinach, squash, turnip, ultilane, chicory, groundnut and zucchini. Angiosperms are divided into two broad classes based on the number of cotyledons, which are seed leaves that generally store or absorb food; a monocotyledonous angiosperm has a single cotyledon, and a dicotyledonous angiosperm has two cotyledons. Angiosperms produce a variety of useful products including materials such as lumber, rubber, and paper; fibers such as cotton and linen; herbs and medicines such as quinine and vinblastine; ornamental flowers such as roses and orchids; and foodstuffs such as grains, oils, fruits and vegetables. Angiosperms encompass a variety of flowering plants, including, for example, cereal plants, leguminous plants, oilseed plants, hardwood trees, fruit-bearing plants and ornamental flowers, which general classes are not necessarily exclusive. Cereal plants, which produce an edible grain cereal, include, for example, corn, rice, wheat, barley, oat, rye, orchardgrass, guinea grass, sorghum and turfgrass. Leguminous plants include members of the pea family (Fabaceae) and produce a characteristic fruit known as a legume. Examples of leguminous plants include, for example, soybean, pea, chickpea, moth bean, broad bean, kidney bean, lima bean, lentil, cowpea, dry bean, and peanut, as well as alfalfa, birdsfoot trefoil, clover and sainfoin. Oilseed plants, which have seeds that are useful as a source of oil, include soybean, sunflower, rapeseed (canola) and cottonseed. Angiosperms also include hardwood trees, which are perennial woody plants that generally have a single stem (trunk). Examples of such trees include alder, ash, aspen, basswood (linden), beech, birch, cherry, cottonwood, elm, eucalyptus, hickory, locust, maple, oak, persimmon, poplar, sycamore, walnut, sequoia, and willow. Trees are useful, for example, as a source of pulp, paper, structural material and fuel. Angiosperms are fruit-bearing plants that produce a mature, ripened ovary, which generally contains seeds. A fruit can be suitable for human or animal consumption or for collection of seeds to propagate the species. For example, hops are a member of the mulberry family that are prized for their flavoring in malt liquor. Fruit-bearing angiosperms also include grape, orange, lemon, grapefruit, avocado, date, peach, cherry, olive, plum, coconut, apple and pear trees and blackberry, blueberry, raspberry, strawberry, pineapple, tomato, cucumber and eggplant plants. An ornamental flower is an angiosperm cultivated for its decorative flower. Examples of commercially important ornamental flowers include rose, orchid, lily, tulip and chrysanthemum, snapdragon, camellia, carnation and petunia plants. The skilled artisan will recognize that the methods of the invention can be practiced using these or other angiosperms, as desired, as well as gymnosperms, which do not produce seeds in a fruit. A method of producing a transgenic plant can be performed by introducing a polynucleotide portion of plant stress-regulated gene into a plant cell genome, whereby the polynucleotide portion of the plant stress-regulated gene modulates a response of the plant cell to a stress condition, thereby producing a transgenic plant, which comprises plant cells that exhibit altered responsiveness to the stress condition. In one embodiment, the polynucleotide portion of the plant stress-regulated gene encodes a stress-regulated polypeptide or functional peptide portion thereof, wherein expression of the stress-regulated polypeptide or functional peptide portion thereof either increases the stress tolerance of the transgenic plant, or decreases the stress tolerance of the transgenic plant. The polynucleotide portion of the plant stress-regulated gene encoding the stress-regulated polypeptide or functional peptide portion thereof can be operatively linked to a heterologous promoter. In another embodiment, the polynucleotide portion of the plant stress-regulated gene comprises a stress-regulated regulatory element. The stress-regulated regulatory element can integrate into the plant cell genome in a site-specific manner, whereupon it can be operatively linked to an endogenous nucleotide sequence, which can be expressed in response to a stress condition specific for the regulatory element; or can be a mutant regulatory element, which is not responsive to the stress condition, whereby upon integrating into the plant cell genome, the mutant regulatory element disrupts an endogenous stress-regulated regulatory element of a plant stress-regulated gene, thereby altering the responsiveness of the plant stress-regulated gene to the stress condition. Accordingly, the invention also provides genetically modified plants, including transgenic plants, produced by such a method, and a plant cell obtained from such genetically modified plant, wherein said plant cell exhibits altered responsiveness to the stress condition; a seed produced by a transgenic plant; and a cDNA library prepared from a transgenic plant. Also provided is a method of modulating the responsiveness of a plant cell to a stress condition. Such a method can be performed, for example, by introducing a polynucleotide portion of a plant stress-regulated gene into the plant cell, thereby modulating the responsiveness of the plant cell to a stress condition. As disclosed herein, the responsiveness of the plant cell can be increased or decreased upon exposure to the stress condition, and the altered responsiveness can result in increased or decreased tolerance of the plant cell to a stress condition. The polynucleotide portion of the plant stress-regulated gene can, but need not, be integrated into the genome of the plant cell, thereby modulating the responsiveness of the plant cell to the stress condition. Accordingly, the invention also provide a genetically modified plant, including a transgenic plant, which contains an introduced polynucleotide portion of a plant stress-regulated gene, as well as plant cells, tissues, and the like, which exhibit modulated responsiveness to a stress condition. The polynucleotide portion of the plant stress-regulated gene can encode a stress-regulated polypeptide or functional peptide portion thereof, which can be operatively linked to a heterologous promoter. As used herein, reference to a “functional peptide portion of a plant stress-regulated polypeptide” means a contiguous amino acid sequence of the polypeptide that has an activity of the full length polypeptide, or that has an antagonist activity with respect to the fall length polypeptide, or that presents an epitope unique to the polypeptide. Thus, by expressing a functional peptide portion of a plant stress-regulated polypeptide in a plant cell, the peptide can act as an agonist or an antagonist of the polypeptide, thereby modulating the responsiveness of the plant cell to a stress condition. A polynucleotide portion of the plant stress-regulated nucleotide sequence also can contain a mutation, whereby upon integrating into the plant cell genome, the polynucleotide disrupts (knocks-out) an endogenous plant stress-regulated nucleotide sequence, thereby modulating the responsiveness of said plant cell to the stress condition. Depending on whether the knocked-out gene encodes an adaptive or a maladaptive stress-regulated polypeptide, the responsiveness of the plant will be modulated accordingly. Thus, a method of the invention provides a means of producing a transgenic plant having a knock-out phenotype of a plant stress-regulated nucleotide sequence. Alternatively, the responsiveness of a plant or plant cell to a stress condition can be modulated by use of a suppressor construct containing dominant negative mutation for any of the stress-regulated sequences described herein. Expression of a suppressor construct containing a dominant mutant mutation generates a mutant transcript that, when coexpressed with the wild-type transcript inhibits the action of the wild-type transcript. Methods for the design and use of dominant negative constructs are well known (see, for example, in Herskowitz, Nature 329:219–222, 1987; Lagna and Hemmati-Brivanlou, Curr. Topics Devel. Biol. 36:75–98, 1998). The polynucleotide portion of the plant stress-regulated gene also can comprise a stress-regulated regulatory element, which can be operatively linked to a heterologous nucleotide sequence, which, upon expression from the regulatory element in response to a stress condition, modulates the responsiveness of the plant cell to the stress condition. Such a heterologous nucleotide sequence can encode, for example, a stress-inducible transcription factor such as DREB1A, which, upon exposure to the stress condition, is expressed such that it can amplify the stress response (see Kasuga et al., supra, 1999). The heterologous nucleotide sequence also can encode a polynucleotide that is specific for a plant stress-regulated gene, for example, an antisense molecule, a ribozyme, and a triplexing agent, either of which, upon expression in the plant cell, reduces or inhibits expression of a stress-regulated polypeptide encoded by the gene, thereby modulating the responsiveness of the plant cell to a stress condition, for example, an abnormal level of cold, osmotic pressure, and salinity. As used herein, the term “abnormal,” when used in reference to a condition such as temperature, osmotic pressure, salinity, or any other condition that can be a stress condition, means that the condition varies sufficiently from a range generally considered optimum for growth of a plant that the condition results in an induction of a stress response in a plant. Methods of determining whether a stress response has been induced in a plant are disclosed herein or otherwise known in the art. A plant stress-regulated regulatory element can be operatively linked to a heterologous polynucleotide sequence, such that the regulatory element can be introduced into a plant genome in a site-specific matter by homologous recombination. For example, a mutant plant stress-regulated regulatory element for a maladaptive stress-induced polypeptide can be transformed into a plant genome in a site specific manner by in vivo mutagenesis, using a hybrid RNA-DNA oligonucleotide (“chimeroplast” ( TIBTECH 15:441–447, 1997; WO 95/15972; Kren, Hepatology 25:1462–1468, 1997; Cole-Strauss, Science 273:1386–1389, 1996, each of which is incorporated herein by reference). Part of the DNA component of the RNA-DNA oligonucleotide is homologous to a nucleotide sequence comprising the regulatory element of the maladaptive gene, but includes a mutation or contains a heterologous region which is surrounded by the homologous regions. By means of base pairing of the homologous regions of the RNA-DNA oligonucleotide and of the endogenous nucleic acid molecule, followed by a homologous recombination the mutation contained in the DNA component of the RNA-DNA oligonucleotide or the heterologous region can be transferred to the plant genome, resulting in a “mutant” gene that, for example, is not induced in response to a stress and, therefore, does not confer the maladaptive phenotype. Such a method similarly can be used to knock-out the activity of a stress-regulated gene, for example, in an undesirable plant. Such a method can provide the advantage that a desirable wild-type plant need not compete with the undesirable plant, for example, for light, nutrients, or the like. A method of modulating the responsiveness of a plant cell to a stress condition also can be performed by introducing a mutation in the chromosomal copy of a plant stress-regulated gene, for example, in the stress-regulated regulatory element, by transforming a cell with a chimeric oligonucleotide composed of a contiguous stretch of RNA and DNA residues in a duplex conformation with double hairpin caps on the ends. An additional feature of the oligonucleotide is the presence of 2′-0-methylation at the RNA residues. The RNA/DNA sequence is designed to align with the sequence of a chromosomal copy of the target regulatory element and to contain the desired nucleotide change (see U.S. Pat. No. 5,501,967, which is incorporated herein by reference). A plant stress-regulated regulatory element also can be operatively linked to a heterologous polynucleotide such that, upon expression from the regulatory element in the plant cell, confers a desirable phenotype on the plant cell. For example, the heterologous polynucleotide can encode an aptamer, which can bind to a stress-induced polypeptide. Aptamers are nucleic acid molecules that are selected based on their ability to bind to and inhibit the activity of a protein or metabolite. Aptamers can be obtained by the SELEX (Systematic Evolution of Ligands by Exponential Enrichment) method (see U.S. Pat. No. 5,270,163), wherein a candidate mixture of single stranded nucleic acids having regions of randomized sequence is contacted with a target, and those nucleic acids having a specific affinity to the target are partitioned from the remainder of the candidate mixture, and amplified to yield a ligand enriched mixture. After several iterations a nucleic acid molecule (aptamer) having optimal affinity for the target is obtained. For example, such a nucleic acid molecule can be operatively linked to a plant stress-regulated regulatory element and introduced into a plant. Where the aptamer is selected for binding to a polypeptide that normally is expressed from the regulatory element and is involved in an adaptive response of the plant to a stress, the recombinant molecule comprising the aptamer can be useful for inhibiting the activity of the stress-regulated polypeptide, thereby decreasing the tolerance of the plant to the stress condition. The invention provides a genetically modified plant, which can be a transgenic plant, that is tolerant or resistant to a stress condition. As used herein, the term “tolerant” or “resistant,” when used in reference to a stress condition of a plant, means that the particular plant, when exposed to a stress condition, shows less of an effect, or no effect, in response to the condition as compared to a corresponding reference plant (naturally occurring wild-type plant or a plant not containing a construct of the present invention). As a consequence, a plant encompassed within the present invention grows better under more widely varying conditions, has higher yields and/or produces more seeds. Thus, a transgenic plant produced according to a method of the invention can demonstrate protection (as compared to a corresponding reference plant) from a delay to complete inhibition of alteration in cellular metabolism, or reduced cell growth or cell death caused by the stress. Preferably, the transgenic plant is capable of substantially normal growth under environmental conditions where the corresponding reference plant shows reduced growth, metabolism or viability, or increased male or female sterility. The determination that a plant modified according to a method of the invention has increased resistance to a stress-inducing condition can be made by comparing the treated plant with a control (reference) plant using well known methods. For example, a plant having increased tolerance to saline stress can be identified by growing the plant on a medium such as soil, which contains a higher content of salt in the order of at least about 10% compared to a medium the corresponding reference plant is capable of growing on. Advantageously, a plant treated according to a method of the invention can grow on a medium or soil containing at least about 50%, or more than about 75%, particularly at least about more than 100%, and preferably more than about 200% salt than the medium or soil on which a corresponding reference plant can grow. In particular, such a treated plant can grow on medium or soil containing at least 40 mM, generally at least 100 mM, particularly at least 200 mM, and preferably at least 300 mM salt, including, for example, a water soluble inorganic salt such as sodium sulfate, magnesium sulfate, calcium sulfate, sodium chloride, magnesium chloride, calcium chloride, potassium chloride, or the like; salts of agricultural fertilizers, and salts associated with alkaline or acid soil conditions; particularly NaCl. In another embodiment, the invention provides a plant that is less tolerant or less resistant to a stress condition as compared to a corresponding reference plant. As used herein, the term “less tolerant” or “less resistant,” when used in reference to a stress condition of a plant, means that the particular plant, when exposed to a stress condition, shows an alteration in response to the condition as compared to a corresponding reference plant. As a consequence, such a plant, which generally is an undesirable plant species, is less likely to grow when exposed to a stress condition than an untreated plant. The present invention also relates to a method of expressing a heterologous nucleotide sequence in a plant cell. Such a method can be performed, for example, by introducing into the plant cell a plant stress-regulated regulatory element operatively linked to the heterologous nucleotide sequence, whereby, upon exposure of the plant cell to stress condition, the heterologous nucleotide sequence is expressed in the plant cell. The heterologous nucleotide sequence can encode a selectable marker, or preferably, a polypeptide that confers a desirable trait upon the plant cell, for example, a polypeptide that improves the nutritional value, digestibility or ornamental value of the plant cell, or a plant comprising the plant cell. Accordingly, the invention provides a transgenic plant that, in response to a stress condition, can produce a heterologous polypeptide from a plant stress-regulated regulatory element. Such transgenic plants can provide the advantage that, when grown in a cold environment for example, expression of the heterologous polypeptide from a plant cold-regulated regulatory element can result in increased nutritional value of the plant. The present invention further relates to a method of modulating the activity of a biological pathway in a plant cell, wherein the pathway involves a stress-regulated polypeptide. As used herein, reference to a pathway that “involves” a stress-regulated polypeptide means that the polypeptide is required for normal function of the pathway. For example, plant stress-regulated polypeptides as disclosed herein include those acting as kinases or as transcription factors, which are well known to be involved in signal transduction pathways. As such, a method of the invention provides a means to modulate biological pathways involving plant stress-regulated polypeptides, for example, by altering the expression of the polypeptides in response to a stress condition. Thus, a method of the invention can be performed, for example, by introducing a polynucleotide portion of a plant stress-regulated gene into the plant cell, thereby modulating the activity of the biological pathway. A method of the invention can be performed with respect to a pathway involving any of the stress-regulated polypeptides as encoded by a polynucleotide of SEQ ID NOS:1–2703, including for example, a stress-regulated transcription factor, an enzyme, including a kinase, a channel protein (see, for example, Tables 29–31; see, also, Table 1). Pathways in which the disclosed stress-regulated stress factors are involved can be identified, for example, by searching the Munich Information Center for Protein Sequences (MIPS) Arabidopsis thaliana database (MATDB), which is at http://www.mips.biochem.mpg.de/proj/thal/. The present invention also relates to a method of identifying a polynucleotide that modulates a stress response in a plant cell. Such a method can be performed, for example, by contacting an array of probes representative of a plant cell genome and nucleic acid molecules expressed in plant cell exposed to the stress; detecting a nucleic acid molecule that is expressed at a level different from a level of expression in the absence of the stress; introducing the nucleic acid molecule that is expressed differently into a plant cell; and detecting a modulated response of the plant cell containing the introduced nucleic acid molecule to a stress, thereby identifying a polynucleotide that modulates a stress response in a plant cell. The contacting is under conditions that allow for selective hybridization of a nucleic acid molecule with probe having sufficient complementarity, for example, under stringent hybridization conditions. As used herein, the term “array of probes representative of a plant cell genome” means an organized group of oligonucleotide probes that are linked to a solid support, for example, a microchip or a glass slide, wherein the probes can hybridize specifically and selectively to nucleic acid molecules expressed in a plant cell. Such an array is exemplified herein by a GeneChip® Arabidopsis Genome Array (Affymetrix; see Example 1). In general, an array of probes that is “representative” of a plant genome will identify at least about 30% or the expressed nucleic acid molecules in a plant cell, generally at least about 50% or 70%, particularly at least about 80% or 90%, and preferably will identify all of the expressed nucleic acid molecules. It should be recognized that the greater the representation, the more likely all nucleotide sequences of cluster of stress-regulated genes will be identified. A method of the invention is exemplified in Example 1, wherein clusters of Arabidopsis genes induced to cold, to increased salinity, to increased osmotic pressure, and to a combination of the above three stress conditions were identified. Based on the present disclosure, the artisan readily can obtain nucleic acid samples for Arabidopsis plants exposed to other stress conditions, or combinations of stress conditions, and identify clusters of genes induced in response to the stress conditions. Similarly, the method is readily adaptable to identifying clusters of stress-regulated genes expressed in other plant species, particularly commercially valuable plant species, where a substantial amount of information is known regarding the genome. The clusters of genes identified herein include those clusters of genes that are induced or repressed in response to a combination of stress conditions, but not to any of the stress conditions alone; and clusters of genes that are induced or repressed in response to a selected stress condition, but not to other stress conditions tested. Furthermore, clusters of genes that respond to a stress condition in a temporally regulated manner are also included, such as gene clusters that are induced early (for example, within about 3 hours), late (for example, after about 8 to 24 hours), or continuously in a stress response. In addition, the genes within a cluster are represented by a variety of cellular proteins, including transcription factors, enzymes such as kinases, channel proteins, and the like (see Tables 1 and 29–31). Thus, the present invention further characterizes nucleotide sequences that previously were known to encode cellular peptides by classifying them within clusters of stress-regulated genes. The present invention additionally relates to a method of identifying a stress condition to which a plant cell was exposed. Such a method can be performed, for example, by contacting nucleic acid molecules expressed in the plant cell and an array of probes representative of the plant cell genome; and detecting a profile of expressed nucleic acid molecules characteristic of a stress response, thereby identifying the stress condition to which the plant cell was exposed. The contacting generally is under conditions that allow for selective hybridization of a nucleic acid molecule with probe having sufficient complementarity, for example, under stringent hybridization conditions. The profile can be characteristic of exposure to a single stress condition, for example, an abnormal level of cold, osmotic pressure, or salinity (Tables 3–14), or can be characteristic of exposure to more than one stress condition (Tables 15–26, for example, cold, increased osmotic pressure and increased salinity (see Tables 24–26). The method can be practiced using at least one nucleic acid probe and can identify one or combination of stress conditions by detecting altered expression of one or a plurality of polynucleotides representative of plant stress-regulated genes. As used herein, the term “at least one” includes one, two, three or more, for example, five, ten, twenty, fifty or more polynucleotides, nucleic acid probes, and the like. The term “plurality” is used herein to mean two or more, for example, three, four, five or more, including ten, twenty, fifty or more polynucleotides, nucleic acid probes, and the like. In a method of the invention, nucleic acid samples from the plant cells to be collected can be contacted with an array, then the profile can be compared with known expression profiles prepared from nucleic acid samples of plants exposed to a known stress condition or combination of stress conditions. By creating a panel of such profiles, representative of various stress conditions, an unknown stress condition to which a plant was exposed can be identified simply by comparing the unknown profile with the known profiles and determining which known profile that matches the unknown profile. Preferably, the comparison is automated. Such a method can be useful, for example, to identify a cause of damage to a crop, where the condition causing the stress is not known or gradually increases over time. For example, accumulation in soils over time of salts from irrigation water can result in gradually decreasing crop yields. Because the accumulation is gradual, the cause of the decreased yield may not be readily apparent. Using the present methods, it is possible to evaluate the stress to which the plants are exposed, thus revealing the cause of the decreased yields. The present invention, therefore includes a computer readable medium containing executable instructions form receiving expression data for sequences substantially similar to any of those disclosed herein and comparing expression data from a test plant to a reference plant that has been exposed to an abiotic stress. Also provided is a computer-readable medium containing sequence data for sequences substantially similar to any of the sequences described herein, or the complements thereof, and a module for comparing such sequences to other nucleic acid sequences. Also provided are plants and plant cells comprising plant stress-regulatory elements of the present invention operably linked to a nucleotide sequence encoding a detectable signal. Such plants can be used as diagnostic or “sentinel” plants to provide early warning that nearby plants are being stressed so that appropriate actions can be taken. In one embodiment, the signal is one that alters the appearance of the plant. For example, an osmotic stress regulatory element of the present invention can be operably linked to a nucleotide sequence encoding a fluorescent protein such as green fluorescent protein. When subjected to osmotic stress, the expression of the green fluorescent protein in the sentinel plant provides a visible signal so that appropriate actions can be taken to remove or alleviate the stress. The use of fluorescent proteins in plants is well known (see, for example, in Leffel et al., BioTechniques 23:912, 1997). The invention further relates to a method of identifying an agent that modulates the activity of a stress-regulated regulatory element of a plant. As used herein, the term “modulate the activity,” when used in reference to a plant stress-regulated regulatory element, means that expression of a polynucleotide from the regulatory element is increased or decreased. In particular, expression can be increased or decreased with respect to the basal activity of the promoter, i.e., the level of expression, if any, in the absence of a stress condition that normally induces expression from the regulatory element; or can be increased or decreased with respect to the level of expression in the presence of the inducing stress condition. As such, an agent can act as a mimic of a stress condition, or can act to modulate the response to a stress condition. Such a method can be performed, for example, by contacting the regulatory element with an agent suspected of having the ability to modulate the activity of the regulatory element, and detecting a change in the activity of the regulatory element. In one embodiment, the regulatory element can be operatively linked to a heterologous polynucleotide encoding a reporter molecule, and an agent that modulates the activity of the stress-regulated regulatory element can be identified by detecting a change in expression of the reporter molecule due to contacting the regulatory element with the agent. Such a method can be performed in vitro in a plant cell-free system, or in a plant cell in culture or in a plant in situ. A method of the invention also can be performed by contacting the agent is contacted with a genetically modified cell or a transgenic plant containing an introduced plant stress-regulated regulatory element, and an agent that modulates the activity of the regulatory element is identified by detecting a phenotypic change in the modified cell or transgenic plant. A method of the invention can be performed in the presence or absence of the stress condition to which the particularly regulatory element is responsive. As such, the method can identify an agent that modulates the activity of plant stress-regulated promoter in response to the stress, for example, an agent that can enhance the stress response or can reduce the stress response. In particular, a method of the invention can identify an agent that selectively activates the stress-regulated regulatory elements of a cluster of plant stress-regulated genes, but does not affect the activity of other stress-regulated regulatory genes. As such, the method provides a means to identify an agent that acts as a stress mimic. Such agents can be particularly useful to prepare a plant to an expected stress condition. For example, a agent that acts as a cold mimic can be applied to a field of plants prior to the arrival of an expected cold front. Thus, the cold stress response can be induced prior to the actual cold weather, thereby providing the plants with the protection of the stress response, without the plants suffering from any initial damage due to the cold. Similarly, an osmotic pressure mimic can be applied to a crop of plants prior a field being flooded by a rising river. In one embodiment, the present invention provides a method for marker-assisted selection. Marker-assisted selection involves the selection of plants having desirable phenotypes based on the presence of particular nucleotide sequences (“markers”). The use of markers allows plants to be selected early in development, often before the phenotype would normally be manifest. Because it allows for early selection, marker-assisted selection decreases the amount of time need for selection and thus allows more rapid genetic progress. Briefly, marker-assisted selection involves obtaining nucleic acid from a plant to be selected. The nucleic acid obtained is then probed with probes that selectively hybridize under stringent, preferably highly stringent, conditions to a nucleotide sequence or sequences associated with the desired phenotype. In one embodiment, the probes hybridize to any of the stress-responsive genes or regulatory regions disclosed herein, for example, any one of SEQ ID NOS:1–2703. The presence of any hybridization products formed is detected and plants are then selected on the presence or absence of the hybridization products. The following examples are intended to illustrate but not limit the invention. EXAMPLE 1 Profiling of Plant Stress-Regulated Genes This example demonstrates that clusters of stress-regulated genes can be identified in plant cells exposed to various stress conditions, either alone or in combination. A GeneChip® Arabidopsis Genome Array (Affymetrix, Santa Clara, Calif.) was used to identify clusters of genes that were coordinately induced in response to various stress conditions. The GeneChip® Arabidopsis Genome Array contains probes synthesized in situ and is designed to measure temporal and spatial gene expression of approximately 8700 genes in greater than 100 EST clusters. The sequences used to develop the array were obtained from GenBank (http://www.ncbi.nlm.nih.gov/) in collaboration with Torrey Mesa Research Institute (San Diego, Calif.), formerly known as Novartis Agriculture Discovery Institute. Eighty percent of the nucleotide sequences represented on the array are predicted coding sequences from genomic BAC entries; twenty percent are high quality cDNA sequences. The array also contains over 100 EST clusters that share homology with the predicted coding sequences from BAC clones (see, for example, world wide web at address (url) “affymetrix.com/products/Arabidopsis_content.html”. The Affymetrix GeneChip® array was used to define nucleotide sequences/pathways affected by various abiotic stresses and to define which are uniquely regulated by one stress and those that respond to multiple stress, and to identify candidate nucleotide sequences for screening for insertional mutants. Of the approximately 8,700 nucleotide sequences represented on the Affymetrix GeneChip® array, 2862 nucleotide sequences showed at least a 2-fold change in expression in at least one sample, relative to no-treatment controls. Of those 2,862 nucleotide sequences 1,335 were regulated only by cold stress, 166 were regulated only mannitol stress and 209 were regulated only by saline stress. Furthermore, of the 2,862 nucleotide sequences 123 nucleotide sequences were regulated by salt and mannitol stress, 293 were regulated by mannitol and cold stress, 274 were regulated by cold and saline stress and 462 were regulated by cold, mannitol and salt. Of the 2,862 nucleotide sequences, 771 passed the higher stringency of showing at least a 2-fold change in expression in at least 2 samples, relative to control. And, 508 of the 771 nucleotide sequences were found in an in-house collection of insertion mutants. The following describes in more detail how the experiments were done. Transcriptional profiling was performed by hybridizing fluorescence labeled cRNA with the oligonucleotides probes on the chip, washing, and scanning. Each gene is represented on the chip by about sixteen oligonucleotides (25-mers). Expression level is related to fluorescence intensity. Starting material contained 1 to 10 μg total RNA; detection specificity was about 1:10 6 ; approximately a 2-fold change was detectable, with less than 2% false positive; the dynamic range was approximately 500×. Nucleotide sequences having up to 70% to 80% identity could be discriminated using this system. Seven day old axenic Arabidopsis seedlings were transferred to Magenta boxes with rafts floating on MS medium. Three weeks later (28 day old seedlings), stresses were applied as follows: Control−no treatment; Cold−Magenta box placed in ice; Mannitol−medium+200 mM mannitol; Salt−medium+100 mM NaCl. Tissue samples were collected at 3 hours and 27 hours into the stress, roots and aerial portions were harvested, RNA was purified, and the samples were analyzed using the GeneChip® Arabidopsis Genome Array (Affymetrix, Santa Clara, Calif.) following the manufacturer's protocol. Raw fluorescence values as generated by Affymetrix software were processed as follows: the values were brought into Microsoft Excel and values of 25 or less were set to 25 (an empirically determined baseline, Zhu and Wang, Plant Physiol. 124:1472–1476; 2000). The values from the stressed samples were then converted to fold change relative to control by dividing the values from the stressed samples by the values from the no-treatment control samples. Expression patterns that were altered at least 2-fold with respect to the control were selected. This method gave very robust results and resulted in a larger number of nucleotide sequences called as stress-regulated than previous methods had permitted. Based on the profiles obtained following hybridization of nucleic acid molecules obtained from plant cells exposed to various stress conditions to the probes in the microarray, clusters of nucleotide sequences that were altered in response to the stress conditions were identified (see Tables 3–6, cold responsive; Tables 7–10, salt (saline) responsive; Tables 11 to 14, mannitol (osmotic) responsive; Tables 15–17, cold and mannitol responsive; Tables 18–20, 6 salt and cold responsive; Tables 21–23, salt and mannitol responsive; Tables 24–26, cold, salt and mannitol responsive. Examples of plant gene sequences that varied in expression at least two-fold in response to a combination of cold, saline and osmotic stress in root cells and leaf cells are shown in Tables 27 and 28, respectively. In addition, examples of plant gene sequences that encode transcription factors (Table 29), phosphatases (Table 30), and kinases (Table 31) and that varied at least two-fold in response to a combination of cold, saline and osmotic stress are provided. Affymetrix ID numbers and corresponding SEQ ID NOS: for the respective Arabidopsis nucleotide sequences are provided Tables 3–26, and can be used to determine SEQ ID NOS: for the sequences shown by Affymetrix ID number in Tables 27–31. The Affymetrix ID number refers to a particular nucleotide sequence on the GeneChip® Arabidopsis Genome Array. In some cases, a particular plant stress-regulated gene sequence hybridized to more than one nucleotide sequence on the GeneChip® Arabidopsis Genome Array (see, for example, Table 3, where SEQ ID NO:36 is shown to have hybridized to the 12187_AT and 15920_I_AT nucleotide sequences on the GeneChip®). In addition, it should be recognized that the disclosed sequences are not limited to coding sequences but, in some cases, include 5′ untranslated sequences (see Table 2) or a longest coding region. As such, while the sequences set forth as SEQ ID NOS:1–2073 generally start with an ATG codon, in most cases each comprises a longer nucleotide sequence, including a regulatory region (see Table 2). The results disclosed herein demonstrate that several polynucleotides, some of which were known to function as transcription factors, enzymes, and structural proteins, also are involved in the response of a plant cell to stress. The identification of the clusters of stress-regulated genes as disclosed herein provides a means to identify stress-regulated regulatory elements present in Arabidopsis thaliana nucleotide sequences, including consensus regulatory elements. It should be recognized, however that the regulatory elements of the plant genes comprising a sequence as set forth in SEQ ID NOS:156, 229, 233, 558, 573, 606, 625, 635, 787, and 813, which previously have been described as cold regulated genes, are not encompassed within the stress-regulated gene regulatory element of the invention, and the regulatory elements of the plant genes comprising the nucleotide sequences set forthas SEQ ID NOS:1263, 1386, 1391, 1405, 1445, 1484, 1589, 1609, 1634, 1726, 1866, 1918, and 1928, which previously have been identified as genes that are responsive to a single stress condition such as cold or saline stress, are not encompassed within the plant stress-regulated gene regulatory elements of the invention to the extent that they confer stress-regulated expression only with respect to the known single stress. Furthermore, the identification of the Arabidopsis stress-regulated genes provides a means to identify the corresponding homologs and orthologs in other plants, including commercially valuable food crops such as wheat, rice, soy, and barley, and ornamental plants. BLASTN and BLASTP searches to identify such sequences revealed the polynucleotide sequences set forth in Table 32, which is on the CD-R compact disc submitted herewith. Although the invention has been described with reference to the above example, it will be understood that modifications and variations are encompassed within the spirit and scope of the invention. Accordingly, the invention is limited only by the claims, which follow Tables 1 to 31. TABLE 1SEQUENCE DESCRIPTIONSSeqSeqIDDescriptionIDDescription1unknown protein1352bZIP transcription factor-likeprotein2unknown protein1353Medicago nodulin N21-like protein3unknown protein1354putative endo-1,4-beta glucanase4putative auxin-induced13551-aminocyclopropane-1-proteincarboxylate oxidase5unknown protein1356putative anion exchange protein6hypothetical protein1357SRG1-like protein7putative protein1358putative protein8unknown protein1359putative phi-1-like phosphate-induced protein9unknown protein1360putative protein10unknown protein1361putative embryo-abundant protein11putative protein1362putative hydrolase12Thioredoxin-like protein1363unknown protein13putative RNA helicase1364unknown protein14putative protein1365hexose transporter-like protein15putative protein1366unknown protein16RING zinc finger protein,1367unknown proteinputative17putative cyclin1368peptide transport-like protein18putative protein1369unknown protein19putative protein1370putative peptide transporter20unknown protein1371disease resistance protein, putative21putative protein1372cysteine protease component ofprotease-inhibitor complex22putative protein1373putative cytochrome P45023hypothetical protein1374putative protein24unknown protein1375hypothetical protein25hypothetical protein1376unknown protein26unknown protein1377putativephosphoribosylaminoimidazolecarboxamide formyltransferase27unknown protein1378putative protein28unknown protein1379HSP like protein29unknown protein1380unknown protein30putative protein1381unknown protein31putative protein1382putative cytochrome P45032putative protein1383similar to pectinesterase33unknown protein1384putative glucosyltransferase34putative ribonuclease III1385thaumatin-like protein35unknown protein1386drought-inducible cysteineproteinase RD19A precursor36unknown protein1387vegetative storage protein Vsp237unknown protein1388unknown protein38unknown protein1389unknown protein39unknown protein1390anthranilate N-benzoyltransferase-likeprotein40putative histidine kinase1391delta-1-pyrroline 5-carboxylase synthetase(P5C1)41scarecrow-like 7 (SCL7)1392glutathione S-conjugatetransporting ATPase(AtMRP1)42putative protein1393hypothetical protein43No function assigned by TIGR1394hypothetical protein44unknown protein1395unknown protein45unknown protein1396putative protein46succinyl-CoA-ligase alpha subunit1397putative protein47putative protein1398No function assigned byTIGR48CLV1 receptor kinase like protein1399unknown protein49putative receptor-like protein1400putative protein kinasekinase50putative squalene synthase1401unknown protein51putative receptor protein kinase1402hypothetical protein52somatic embryogenesis receptor-1403unknown proteinlike kinase, putative53putative protein1404putative calcium-bindingEF-hand protein54putative beta-glucosidase1405cinnamyl-alcoholdehydrogenase ELI3-155multi-drug resistance protein1406putative protein56receptor protein kinase (TMK1),1407unknown proteinputative57putative receptor-like protein1408senescence-associatedkinaseprotein sen158putative pectate lyase1409hypothetical protein59putative protein kinase1410putative cytochrome P45060putative peroxidase1411proline oxidase,mitochondrial precursor(osmotic stress-inducedproline dehydrogenase)61cytochrome P450-like protein1412putative response regulator362putative beta-amylase1413hypothetical protein63monosaccharide transporter STP31414glutamine-dependentasparagine synthetase64Lycopersicon esculentum1415lysine-ketoglutarateproteinase TMP, Pir2:T07617reductase/saccharopine65putative receptor-like protein1416En/Spm-like transposonkinaseprotein66G-box-binding factor 11417G-box binding bZIP transcriptionfactor67amino acid carrier, putative1418putative protein68myb-related protein1419putative protein69No function assigned by TIGR1420putative protein70SNF1 like protein kinase1421ATFP4-like71Cu/Zn superoxide dismutase-like1422unknown proteinprotein72putative protein kinase1423unknown protein73small nuclear ribonucleoprotein1424putative proteinU1A74ras-like GIF-binding1425invertase inhibitor homologprotein(emb|CAA73335.1)75oleoyl-[acyl-carrier-protein]1426unknown proteinhydrolase-like protein76putative heat shock1427unknown proteintranscription factor77putative protein1428putative cytochrome b578membrane-bound small1429putative proteinGTP-binding-like protein79putative protein (fragment)1430putative protein80indole-3-acetate beta-1431putative proteinglucosyltransferase likeprotein81HD-zip transcription factor1432No function assigned by TIGR(athb-8)82putative cAMP-dependent1433putative copper/zinc superoxideprotein kinasedismutase83glucuronosyl transferase-1434protein phosphatase ABI1like protein84putative leucine-rich repeat1435glutamate dehydrogenase 2disease resistance protein8598b like protein1436No function assigned by TIGR86putative receptor-like1437low-temperature-induced proteinprotein kinase78 (sp|Q06738)87IAA-Ala hydrolase (IAR3)1438putative myo-inositol 1-phosphatesynthase88putative AP2 domain1439phosphate transportertranscription factor(gb|AAB17265.1)89putative expansin14404-hydroxyphenylpyruvatedioxygenase (HPD)90putative Ap2 domain1441histone H1protein91expansin (At-EXP1)1442hypothetical protein92cytochrome P450-like1443No function assigned by TIGRprotein93putative ATP-dependent1444neoxanthin cleavage enzyme-likeRNA helicase Aprotein94unknown protein1445dehydration-induced protein RD2295predicted protein1446zinc finger protein ZAT796putative glucosyltransferase1447unknown protein97unknown protein1448unknown protein98putative xyloglucan-1449unknown proteinspecific glucanase99cysteine synthase1450unknown protein100clathrin assembly protein1451putative proteinAP19 homolog101dynein light chain like protein1452putative protein102chaperonin CPN101453RNA helicase, putative103putative bHLH transcription factor1454putative glycine-richprotein104putative glyoxysomal malate1455hypothetical proteindehydrogenase precursor105ATP-dependent RNA helicase,1456putative proteinputative106chlorophyll synthetase1457peroxidase107similar to epoxide hydrolases1458peroxidase ATP3a(emb|CAA67340.1)108putative protein1459metallothionein-like protein109unknown protein1460endomembrane-associatedprotein110hypothetical protein1461ferritin 1 precursor111putative membrane transporter1462dehydrin RAB18-likeprotein (sp|P30185)112putative tyrosyl-tRNA synthetase1463HSR201 like protein113ARGININE/SERINE-RICH1464light regulated protein,SPLICING FACTOR RSP31putative114putative oxidoreductase1465Dr4 (protease inhibitor)115unknown protein1466mitogen activated proteinkinase kinase (nMAPKK)116linker histone protein, putative1467glutathione S-transferase117hypothetical protein1468transcriptional activatorCBF1/CRT/CRE bindingfactor 1118putative protein1469homeobox-leucine zipperprotein ATHB-12119putative mitochondrial carrier1470amino acid permease Iprotein120putative transcription factor1471MAP kinase (ATMPK7)121MYB-related protein1472potassium channel proteinAKT3122myb-related transcription factor,1473cytochrome P450putativemonooxygenase(CYP91A2)123unknown protein1474putative transport protein124unknown protein1475putative protein125putative glycine-rich protein1476hypothetical protein126No function assigned by TIGR1477putative protein127unknown protein1478hypothetical protein128unknown protein1479receptor protein kinase-likeprotein129unknown protein1480serine/threonine proteinkinase-like protein130unknown protein1481putative auxin-regulatedprotein131putative membrane channel protein1482amino acid transport proteinAAP2132putative protein1483unknown protein133unknown protein1484cold and ABA inducible proteinkin1134gamma glutamyl hydrolase,1485gamma-VPE (vacuolar processingputativeenzyme)13540S ribosomal protein S51486putative protein 1 photosystem IIoxygen-evolving complex136DnaJ-like protein1487myrosinase-associated protein,putative13740S ribosomal protein S261488transcription factor ATMYB4138putative WRKY-type DNA binding1489H-protein promoter binding factor-protein2a139putative protein1490ammonium transporter, puitative140hypothetical protein1491putative zeta-carotene desaturaseprecursor141putative ubiquitin-1492high-affinity nitrate transporterconjugating enzymeNRT2142peptidylprolyl isomerase1493light induced protein likeROC1143glyceraldehyde-3-1494putative AT-hook DNA-bindingphosphate dehydrogenase Cproteinsubunit (GapC)144No function assigned by1495putative glycogeninTIGR145putative protein1496putative light repressible receptorprotein kinase146putative thioredoxin1497serine/threonine kinase-likeprotein147thioredoxin h, putative1498putative peroxidase148thioredoxin-like1499cytochrome P450 monooxygenase(CYP83A1)149allene oxide synthase1500MYB-related transcription factor(emb|CAA73184.1)(CCA1)150anthranilate synthase1501Terminal flower1 (TFL1)component I-1 precursor(sp|P32068)151CELL DIVISION1502sulfate transporter ATST1CONTROL PROTEIN 2HOMOLOG A152protein kinase cdc21503RING-H2 finger protein RHA3bhomolog B153ethylene responsive1504lipoxygenase, putativeelement binding factor 1(frameshift !)154ethylene responsive1505serine O-acetyltransferase (ECelement binding factor 22.3.1.30) Sat-52 (pir||S71207)(ATERF2) (sp|O80338)155ethylene responsive1506ferulate-5-hydroxylase (FAH1)element binding factor 5(ATERF5) (sp|O80341)156glucose-6-phosphate1507En/Spm-like transposon protein,dehydrogenaseputative157photomorphogenesis1508calmodulin-binding-like proteinrepresser (COP1)158unknown protein1509hypothetical protein159DNA (cytosine-5)- methyltransferase (DNA1510somatic embryogenesis receptor-methyltransferase) (DNAlike kinase-like proteinmetase) (sp|P34881)160PROLIFERA1511putative giberellin beta-hydroxylase161putative photomorphogenesis1512putative pectinesteraserepresser protein162SNF1-like protein kinase (AKin11)1513putative protein163thioredoxin h1514unknown protein164thioredoxin1515ribosomal protein165Ca2+-dependent lipid-binding1516low-temperature-inducedprotein, putative65 kD protein (sp|Q04980)166putative auxin-induced protein1517putative glucosyltransferase167putative bZIP transcription factor1518peroxidase(emb|CAA67551.1)168hypothetical protein1519ankyrin-like protein169putative AVR9 elicitor response1520ribosomal protein S11-likeprotein170putative serine/threonine protein1521hypothetical proteinkinase171bZIP transcription factor ATB21522glycoprotein (EP1), putative172putative spliceosome associated1523calnexin-like proteinprotein1733-hydroxyisobutyryl-coenzyme A1524SRG1-like proteinhydrolase-like protein174putative protein1525ethylene response factor 1(ERF1)175putative Mutator-like transposase1526transcriptional activatorCBF1-like protein176putative protein1527xyloglucan endo-1,4-beta-D-glucanase (XTR-6)177unknown protein1528putative cinnamyl alcoholdehydrogenase178putative protein1529gibberellin 3 beta-hydroxylase, putative179putative protein1530auxin response transcriptionfactor 3 (ETTIN/ARF3)180putative galactinol synthase1531No function assigned byTIGR181putative transcriptional regulator1532putative protein182nuclear matrix constituent protein 11533similar to avrRpt2-induced(NMCP1)-likeprotein 1183putative DNA-binding protein1534unknown proteinRAV2184No function assigned by TIGR1535hypothetical protein185basic blue protein, 5′ partial1536putative protein kinase186unknown protein1537respiratory burst oxidase-like protein187putative calcium-binding protein,1538glucose-6-calreticulinphosphate/phosphate-translocator precursor,putative188putative pyrophosphate-fructose-6-1539class 1 non-symbioticphosphate 1-phosphotransferasehemoglobin (AHB1)189ribosomal protein L11, cytosolic1540endochitinase isolog190putative dTDP-glucose 4-6-1541putative cytochrome P450dehydratase19140S ribosomal protein S20-like154260S acidic ribosomal protein P0protein19260S ribosomal protein L241543putative protein193coatomer-like protein,1544auxin-induced protein, putativeepsilon subunit194glycoprotein (EP1), putative1545unknown protein195putative SPL1-related1546hypothetical proteinprotein196unknown protein1547protein phosphatase 2C ABI2(PP2C) (sp|O04719)197putative transport protein1548peroxidase, prxr2SEC61 beta-subunit198unknown protein1549putative peroxidase ATP12a199putative cytochrome P4501550putative beta-amylase200UTP-glucose1551putative acetone-cyanohydrin lyaseglucosyltransferase-likeprotein20160S ribosomal protein L231552fatty acid elongase 3-ketoacyl-CoAsynthase 120240S ribosomal protein S171553putative citrate synthase20340S ribosomal protein S261554pEARLI 1-like protein204protein translation factor1555putative MYB family transcriptionSui1 homolog, putativefactor205unknown protein1556putative transcription factorMYB28206gamma glutamyl hydrolase,1557RNA helicase-like proteinputative207dTDP-glucose 4,6-1558snoRNAdehydratase, putative208extensin-like protein1559putative protein kinase209unknown protein1560growth regulator like protein210protein phosphatase 2C-1561putative potassium transporterlike protein211ubiquitin-like protein1562putative protein212protein phosphatase 2C-like156360S ribosomal protein L14protein213unknown protein1564unknown protein214putative RING zinc finger1565putative RING-H2 zinc fingerankyrin proteinprotein215unknown protein1566putative pollen surface protein216putative rubisco subunit1567unknown proteinbinding-protein alphasubunit217putative acetone-1568unknown proteincyanohydrin lyase218putative isoamylase1569unknown protein219putative protein1570putative Ca2+-ATPase220HSP associated protein like15711-aminocyclopropane-1-carboxylate synthase-like protein22160S ribosomal protein L391572putative beta-glucosidase222unknown protein1573transcription factor ZAP1223putative SF16 protein { Helianthus1574oligopeptide transporter, putativeannuus }224unknown protein1575putative protein225thioredoxin1576putative glucosyltransferase226trehalose-6-phosphate phosphatase1577putative serine/threonine kinase(AtTPPB)227chlorophyll a/b-binding protein1578squalene epoxidase-like protein228class IV chitinase (CHIV)1579similar to 14 KD proline-richprotein DC2.15 precursor(sp|P14009); similar toESTs emb|Z17709 andemb|Z47685229chalcone synthase (naringenin-1580unknown proteinchalcone synthase) (testa 4 protein)(sp|P13114)230unknown protein1581unknown protein231cinnamyl-alcohol dehydrogenase1582hypothetical proteinELI3-2232farnesyl-pyrophosphate synthetase158360S ribosomal protein L38FPS2233phospholipid hydroperoxide1584flavin-containingglutathione peroxidasemonooxygenase, putative234heat shock transcription factor1585remorinHSF4235heat shock protein 1011586unknown protein23617.6 kDa heat shock protein (AA1587putative protein1-156)237heat shock protein 17.6A1588lipoxygenase238heat-shock protein1589cold-regulated proteinCOR6.6 (KIN2)239HY51590Myb transcription factorhomolog (ATR1)240putative auxin-induced protein,1591putative proteinIAA12241early auxin-induced protein,1592unknown proteinIAA19242auxin-inducible gene (IAA2)1593unknown protein243putative protein1594Ca2+-transporting ATPase-like protein244putative choline kinase1595protein phosphatase 2C(AtP2C-HA)245thymidylate kinase-like protein1596peroxidase ATP24a246CTP synthase like protein1597branched-chain alpha keto-acid dehydrogenase,putative247putative protein1598putative beta-ketoacyl-CoAsynthase248putative amidase1599putative protein2494-alpha-glucanotransferase1600putative beta-galactosidase250hypothetical protein1601putative protein251similar to auxin-induced protein160260S ribosomal protein L27252putative protein1603putative annexin253putative protein1604NAC domain protein,putative254putative protein1605unknown protein255hyuC-like protein1606late embryogenesisabundant protein LEA like256putative tetracycline1607unknown proteintransporter protein257similar to early nodulins1608putative protein258putative protein1609dehydrin Xero2259putative peptidyl-prolyl cis-1610putative zinc finger proteintrans isomerase260unknown protein1611unknown protein261unknown protein1612DnaJ-like protein262putative endochitinase1613putative inositol polyphosphate-5-phosphatase263putative ABC transporter1614putative cytochrome P450264No function assigned by1615putative proteinTIGR265CONSTANS-like B-box1616unknown proteinzinc finger protein266unknown protein1617putative protein267unknown protein1618hypothetical protein268putative mitochondrial1619putative proteinprocessing peptidase alphasubunit269putative pre-mRNA1620sucrose-UDP glucosyltransferasesplicing factor270putative phosphatidylserine1621glucose-6-phosphate 1-decarboxylasedehydrogenase271unknown protein1622unknown protein272unknown protein1623mitochondrial chaperonin (HSP60)273unknown protein1624sucrose transport protein SUC1274putative casein kinase I1625putative protein disulfide isomerase275unknown protein1626putative pollen-specific protein27660S ribosomal protein1627integral membrane protein,L23Aputative277putative mitochondrial1628rubredoxin, putativedicarboxylate carrierprotein278enoyl-ACP reductase (enr-1629putative proteinA)279putative isoamylase1630disease resistance protein RPS4,putative280formamidase-like protein1631putative peptide/amino acidtransporter281reticuline oxidase-like1632peroxidase, putativeprotein282unknown protein1633ethylene receptor, putative (ETR2)283putative transketolase1634protein phosphatase 2C (PP2C)precursor284putative protein1635putative glutathione S-transferase285unknown protein1636homeodomain transcription factor(ATHB-7)286unknown protein1637putative nitrate transporter287unknown protein1638putative ribosomal protein L9,cytosolic288putative esterase D1639putative DNA-binding protein289predicted protein of unknown1640beta-1,3-glucanase-like proteinfunction290unknown protein1641putative zinc transporter291putative indole-3-glycerol1642transcription factor TINYphosphate synthase292isopentenyl1643putative aspartate kinase-pyrophosphate:dimethyllallylhomoserine dehydrogenasepyrophosphate isomerase293kinase associated protein1644ethylene reponse factor-like AP2phosphatasedomain transcription factor294putative K+ channel, beta subunit1645peptide transporter-like protein295KNAT1 homeobox-like protein1646trehalose-6-phosphate synthase likeprotein296PSI type II chlorophyll a/b-binding1647putative ribonucleaseprotein, putative297transcription factor1648hypothetical protein298putative WD-40 repeat protein,1649putative DNA-bindingMSI2protein299WD-40 repeat protein (MSI3)1650nodulin-like protein300putative WD-40 repeat protein,1651trehalose-6-phosphateMSI4phosphatase-like protein301unknown protein1652succinate dehydrogenaseflavoprotein alpha subunit(emb|CAA05025.1)302hypothetical protein1653unknown protein303putative protein1654stress related protein,putative304No function assigned by TIGR1655putative chloroplastinitiation factor 3305polyphosphoinositide binding1656putative proteinprotein, putative306hypothetical protein1657hypothetical protein307unknown protein1658putative CCCH-type zincfinger protein308chloroplast ribosomal L1-like1659similar to harpin-inducedproteinprotein hin1 from tobacco309cold-regulated protein cor15b1660unknown proteinprecursor310cyanohydrin lyase like protein1661unknown protein311putative replication protein A11662hypothetical protein312putative protein1663No function assigned byTIGR313possible apospory-associated like1664putative proteinprotein314DNA binding protein GT-1,1665putative glutathione S-putativetransferase TSI-1315AT-hook DNA-binding protein1666putative protein(AHP1)316putative phospholipase1667putative PTR2 familypeptide transporter317chloroplast FtsH protease, putative1668receptor kinase-like protein318enoyl-CoA hydratase like1669putative sugar transportproteinprotein, ERD6319berberine bridge enzyme-1670putative proteinlike protein320putative sugar transporter1671nodulin-like protein321unknown protein1672unknown protein322No function assigned by1673putative receptor-likeTIGRprotein kinase323hypothetical protein1674glutathione-conjugatetransporter AtMRP4324putative acidic ribosomal1675ascorbate oxidase-likeproteinprotein325putative protein1676pathogenesis-related protein 1precursor, 19.3K326unknown protein1677R2R3-MYB transcription factor327hypothetical protein1678hypothetical protein328putative protein1679putative chitinase329dihydroxypolypreny1680Mlo protein, putativelbenzoate methyltransferase330unknown protein1681putative WRKY-type DNA bindingprotein331myb-related protein1682putative acyl-CoA synthetase332No function assigned by1683putative pathogenesis-relatedTIGRprotein333putative protein1684putative chitinase334putative disease resistance1685germin precursor oxalate oxidaseresponse protein335hypothetical protein1686endoxyloglucan transferase,putative336No function assigned by1687putative proteinTIGR337starch branching enzyme II1688putative cytochrome P450338No function assigned by1689similar to Mlo proteins from H.TIGRvulgare339putative enolase (2-1690putative tropinone reductasephospho-D-glyceratehydroylase)340putative protein kinase1691extensin-like protein341HD-Zip protein, putative1692putative sarcosine oxidase342putative protein kinase1693putative protein343phenylalanyl-trna1694hypothetical proteinsynthetase-like protein344putative aconitase1695late embryogenesis-abundantprotein, putative345NAM (no apical meristem)1696beta-carotene hydroxylaseprotein, putative346unknown protein1697putative calcium binding protein347putative1698unknown proteinphosphomannomutase348putative farnesylated protein1699unknown protein349unknown protein1700predicted glycosyl transferase350water stress-induced protein,1701hypothetical proteinputative351unknown protein1702hypothetical protein352unknown protein1703hypothetical protein353PEROXISOMAL MEMBRANE1704putative proteinPROTEIN PMP22354putative peroxisomal membrane1705unknown proteincarrier protein355putative protein1706putative protein356unknown protein1707putative protein357putative protein1708serine/threonine kinase-likeprotein358putative protein1709No function assigned by TIGR359argininosuccinate synthase-like1710putative pectinesteraseprotein3601-phosphatidylinositol-4,5-1711peroxidase like proteinbisphosphate phosphodiesterase361putative JUN kinase activator1712No function assigned by TIGRprotein362putative 60S ribosomal protein L351713phenylalanine ammonialyase (PALI)363nucleoid DNA-binding protein1714peroxidasecnd41-like protein(emb|CAA68212.1)364SigA binding protein1715putative AMP deaminase365hypothetical protein1716putative MYB familytranscription factor366putative protein kinase1717DNA-directed RNApolymerase II, third largest subunit367unknown protein1718nucleotide pyrophosphatase-like protein368regulatory protein NPR1-like;1719putative peroxidasetranscription factor inhibitor Ikappa B-like369putative protein1720calcium sensor homolog(gb|AAC26110.1)370hypothetical protein1721putative GDSL-motiflipase/hydrolase371phosphoribosylanthranilate1722putative nonspecific lipid-isomerasetransfer protein372phosphoribosylanthranilate1723acyl-carrier protein (ACP),isomeraseputative373sterol glucosyltransferase, putative1724putative glycinedehydrogenase374putative gigantea protein1725AIG1375putative MYB family transcription1726ACC synthase (AtACS-6)factor376hypothetical protein1727cyclin delta-3377hypothetical protein1728putative RING zinc fingerprotein378predicted protein1729aldose 1-epimerase-likeprotein379cytochrome P450, putative1730putative phospholipase380putative Na+ dependent1731phosphoenolpyruvateileal bile acid transportercarboxylase381unknown protein1732putative galactinol synthase382RING-H2 finger protein1733unknown proteinRHF1a383putative protein1734putative protein384unknown protein17351-aminocyclopropane-1-carboxylate oxidase385putative protein1736thioredoxin (clone GIF1)(pir||S58118)386putative auxin-regulated1737trehalose-6-phosphateproteinphosphatase387hypothetical protein1738beta-1,3-glucanase 2 (BG2)(PR-2)388unknown protein1739putative S-adenosyl-L-methionine:trans-caffeoyl-Coenzyme A 3-O-methyltransferase389unknown protein1740disease resistance protein EDS1390putative protein1741putative protein kinase391putative protein1742Gluthatione reductase, chloroplastprecursor392unknown protein1743putative heat shock protein393histone H11744aspartate kinase394Argonaute (AGO1)-like1745putative major intrinsic (channel)proteinprotein395unknown protein1746matrix metalloproteinase, putative396putative protein with C-1747putative GDSL-motifterminal RING fingerlipase/hydrolase397unknown protein1748putative protein398unknown protein1749DAG-like protein399unknown protein1750serine/threonine kinase-likeprotein400unknown protein1751formamidase-like protein401unknown protein1752CER2402putative copper amine175326S proteasome subunit 4oxidase403unknown protein1754pectinesterase like protein404unknown protein1755putative disease resistance protein405unknown protein1756putative RNA methyltransferase406putative protein1757unknown protein407putative protein1758HOMEOBOX PROTEINKNOTTED-1 LIKE 4 (KNAT4)408unknown protein1759glycine-rich RNA-binding proteinAtGRP2-like409unknown protein1760putative acetylornithinetransaminase410putative protein1761putative Sec24-like COPII protein411putative protein1762putative berberine bridge enzyme412unknown protein1763putative GH3-like protein413serine/threonine kinase-1764putative ABC transporterlike protein414alcohol dehydrogenase,1765putative reticuline oxidase-likeputativeprotein415anthranilate1766pectate lyase-like proteinphosphoribosyltransferase,chloroplast precursor (sp|Q02166)416phytochrome C (sp|P14714)1767protein disulfide-isomerase-likeprotein417putative phytochrome-associated1768putative proteinprotein 3418receptor serine/threonine kinase1769putative membrane transporterPR5K419Ran-binding protein (atranbp1a)1770unknown protein420small Ras-like GTP-binding1771unknown proteinprotein (gb|AAB58478.1)421sterol-C5-desaturase1772putative RING-H2 zinc fingerprotein422tryptophan synthase beta chain 11773unknown proteinprecursor (sp|P14671)423thioredoxin f2 (gb|AAD35004.1)1774unknown protein424No function assigned by TIGR1775unknown protein425putative WRKY DNA-binding1776MADS-box proteinprotein(AGL20)426putative protein1777amidophosphoribosyltransfer-ase 2 precursor427unknown protein1778putative dihydrodipicolinatesynthase428unknown protein1779hypothetical protein42914-3-3 protein homolog RCI11780ABA-responsive protein-(pir||S47969)like430unknown protein1781putative protein431putative CCCH-type zinc finger1782hypothetical proteinprotein432PINHEAD (gb|AAD40098.1);1783DNA-binding protein-liketranslation initiation factor433plasma membrane proton ATPase1784No function assigned by(PMA)TIGR434CHLOROPHYLL A-B BINDING1785transcription factor,PROTEIN 4 PRECURSORputativehomolog435membrane related protein CP5,1786nitrate reductase, putativeputative436ABC transporter (AtMRP2)1787putative protein437putative embryo-abundant protein1788putative protein438putative anthocyanidin-3-glucoside1789putative proteinrhamnosyltransferase439putative lipid transfer protein1790putative protein440unknown protein1791unknown protein441unknown protein1792unknown protein442galactinol synthase, putative1793tryptophan synthase beta-subunit (TSB2)443putative protein1794hypothetical protein444putative protein1795putative protein445SCARECROW-like protein1796putative DNA-bindingprotein446unknown protein1797putative 40S ribosomalprotein S10447unknown protein1798putative protein448unknown protein1799putative cytochrome P450449unknown protein1800putative protein450asparagine--tRNA ligase1801putative protein451putative protein1802putative glucosyltransferase452glutamate-1-semialdehyde1803No function assigned by2,1-aminomutase 1TIGRprecursor (GSA 1)(glutamate-1-semialdehydeaminotransferase 1) (GSA-AT 1) (sp|P42799)453hypothetical protein1804putative protein454putative serine protease-like1805putative proteinprotein455No function assigned by1806unknown proteinTIGR456unknown protein1807glycine-rich RNA binding protein7457unknown protein1808dehydrin, putative458gamma-adaptin, putative1809putative endoxyloglucanglycosyltransferase459UDP rhamnose--1810glutamate decarboxylase 1 (GADanmocyanidin-3-glucoside1) (sp|Q42521)rhamnosyltransferase-likeprotein460carbonate dehydratase-like1811delta 9 desaturaseprotein461putative microtubule-1812UDP-glucose glucosyltransferaseassociated protein462putative ribophorin I1813CARBONIC ANHYDRASE 2463putative zinc finger protein1814response reactor 2 (ATRR2)464chloroplast FtsH protease,1815S-adenosyl-methionine-sterol-C-putativemethyltransferase, putative465putative protein1816putative DNA-binding protein(RAV2-like)466unknown protein1817gamma glutamyl hydrolase,putative467putative LEA protein1818protein phosphatase-like468putative protein1819unknown protein469putative protein1820unknown protein470unknown protein1821unknown protein471putative purple acid1822copper transport protein-likephosphataseprotein472unknown protein1823hypothetical protein473putative protein1824unknown protein474unknown protein1825putative peptide methioninesulfoxide reductase475chlorophyll binding protein,1826putative obtusifoliol 14-alphaputativedemethylase476phosphoenolpyruvate carboxylase1827glutamate dehydrogenase (EC(PPC)1.4.1.-) 1 (pir||S71217)477chlorophyll a/b-binding protein-1828unknown proteinlike478AtAGP41829xyloglucan endo-1,4-beta-D-glucanase precursor479putative cryptochrome 2 apoprotein1830unknown protein480type 2 peroxiredoxin, putative1831SNF1 related protein kinase(ATSRPK1)481Atpm24.1 glutathione S transferase1832putative protein482delta tonoplast integral protein1833putative chloroplast nucleoid DNA(delta-TIP)binding protein48320S proteasome subunit (PAA2)1834hypothetical protein484dormancy-associated protein,1835putative proteinputative485putative cytidine deaminase1836putative thiamin biosynthesisprotein486No function assigned by TIGR1837unknown protein487putative phospholipase D-gamma1838unknown protein488cell elongation protein, Dwarf11839putative RNA helicase489germin-like protein1840putative SF21 protein{ Helianthus annuus }490hevein-like protein precursor (PR-1841unknown protein4)491rac-like GTP binding protein1842NBS/LRR disease(ARAC5)resistance protein, putative492phosphoprotein phosphatase, type1843hypothetical protein1 catalytic subunit493ubiquitin-protein ligase UBC91844unknown protein494xyloglucan endotransglycosylase-1845No function assigned byrelated protein XTR-7TIGR495cysteine synthase1846glycine-rich protein(AtGRP2)496putative villin 21847No function assigned byTIGR497glutathione S-transferase1848putative protein4985-adenylylsulfate reductase1849putative glucosyltransferase499arginine decarboxylase1850hypothetical protein500ATHP2, putative1851hypothetical protein501ornithine carbamoyltransferase1852putative proteinprecursor502puative protein1853putative disease resistanceprotein503putative protein1854thaumatin, putative504unknown protein1855putative proline-rich protein505putative protein1856sterol-C-methyltransferase506putative protein1857superoxidase dismutase507unknown protein1858TINY-like protein508unknown protein1859calcium-dependent proteinkinase, putative509unknown protein1860hypothetical protein510unknown protein1861putative protein kinase511hypothetical protein1862DNA-directed RNApolymerase (mitochondrial)512putative protein1863putaive DNA-bindingprotein513putative DnaJ protein1864late embryogenesisabundant M17 protein514plastocyanin1865putative protein515unknown protein1866delta-1-pyrroline-5-carboxylate synthetase516unknown protein1867putative 60s ribosomalprotein L10517unknown protein1868cytochrome P450CYP86A1518unknown protein1869putative tyrosine aminotransferase519unknown protein1870thionin520unknown protein1871No function assigned by TIGR521putative ATP-dependent1872APETALA2 proteinRNA helicase522non-race specific disease1873MADS-box protein (AGL3)resistance protein (NDR1)523hypothetical protein1874putative monooxygenase524putative protein1875ZFP3 zinc finger protein525putative protein1876cell division protein FtsZchloroplast homolog precursor(sp|Q42545)526putative protein1877calreticulin, putative527copper transport protein1878phosphoserine aminotransferase528putative protein187912-oxophytodienoate-10,11-reductase529unknown protein1880putative bHLH transcription factor530unknown protein1881pectin methylesterase (PMEU1),putative531unknown protein1882DNA-binding protein532putative protein kinase1883carnitine racemase like protein533unknown protein1884putative protein534putative protein1885endoxyloglucan transferase(dbj|BAA81669.1)535putative protein1886RMA1 RING zinc finger protein536hypothetical protein1887ammonium transporter537putative protein1888apyrase (gb|AAF00612.1)538putative AP2 domain1889potassium uptake transporter-liketranscription factorprotein539putative nitrilase1890putative ABC transporter540putative protein1891potassium transporter-like protein541putative tetrahydrofolate1892integral membrane protein,synthaseputative542heat-shock protein1893putative protein543unknown protein1894pyruvate decarboxylase-1 (Pdc1)544unknown protein1895putative malate oxidoreductase545histone H41896putative histone H2B546hypothetical protein1897snoRNA547unknown protein1898symbiosis-related like protein548putative protein1899unknown protein549predicted protein1900unknown protein550putative dihydrolipoamide1901hypothetical proteinsuccinyltransferase551actin 31902putative protein552putative CCCH-type zinc finger1903copper-binding protein-likeprotein553MAP kinase kinase 21904putative protein554ethylene-insensitive3-like1 (EIL1)1905unknown protein555histidine transport protein (PTR2-1906putative glyoxalase IIB)556putative auxin-induced protein1907No function assigned byAUX2-11TIGR557hydroxyacylglutathione hydrolase1908hypothetical proteincytoplasmic (glyoxalase II) (GLXII)558delta-8 sphingolipid desaturase1909flavanone 3-hydroxylase(FH3)559cellulose synthase catalytic subunit1910putative laccase(Ath-A)560nitrate transporter (NTL1)1911putative protein kinase561DNA-binding homeotic protein1912myb-related protein, 33.3KAthb-2(pir||S71284)562hypothetical protein1913unknown protein563aspartate aminotransferase1914endo-xyloglucan transferase-like protein5644-coumarate:CoA ligase 11915TMV resistance protein N-like565pyruvate dehydrogenase E1 beta1916putative xyloglucansubunit, putativeendotransglycosylase566nucleotide diphosphate kinase Ia1917unknown protein(emb|CAB58230.1)567chloroplast Cpn21 protein1918proline transporter 2568ATP dependent copper transporter1919resistance protein, putative569very-long-chain fatty acid1920actin, putativecondensing enzyme (CUT1)570putative purine-rich single-stranded1921putative related to microbialDNA-binding proteindivalent cation toleranceproteins571serine/threonine protein1922unknown proteinphosphatase (type 2A)572isopentenyl1923putative glycosyldiphosphate:dimethylallyltransferasediphosphate isomerase (IPP2)573putative c2h2 zinc finger1924unknown proteintranscription factor574putative 20S proteasome beta1925putative proteinsubunit PBC2phosphatase 2C575nucleoside diphosphate kinase 31926unknown protein(ndpk3)576ras-related small GTP-binding1927serpin, putativeprotein577putative 4-coumarate:CoA ligase 21928cinnamyl-alcoholdehydrogenase CAD1578transcription factor HBP-1b1929putative protein importhomolog (sp|P43273)receptor579biotin synthase (Bio B)1930unknown protein580homeobox protein HAT221931unknown protein581putative preprotein1932putative proteintranslocase SECY protein582carbamoylphosphate1933putative CDP-synthetase, putativediacylglycerol--glycerol-3-phosphate 3-phosphatidyltransferase583putative protein kinase,1934unknown proteinADK1584putative nuclear DNA-1935putative LRR receptor-likebinding protein G2pprotein kinase585hypothetical protein1936serine/threonine protein kinase,putative586hypothetical protein1937potassium transporter-like protein587unknown protein1938lactate dehydrogenase (LDH1)588unknown protein1939hypothetical protein589molybdopterin synthase1940unknown protein(CNX2)590putative ribosomal protein1941putative thaumatinL6591unknown protein1942putative reticuline oxidase-likeprotein592En/Spm-like transposon1943uracil phosphoribosyltransferase,proteinputative593putative protein1944transcription factor, putative594putative protein1945unknown protein595unknown protein1946unknown protein596hypothetical protein1947GATA transcription factor 4597unknown protein1948unknown protein598unknown protein1949unknown protein599putative lysosomal acid1950senescence-associated protein-likelipase600unknown protein1951putative pollen allergen601unknown protein1952unknown protein602NifS-like aminotranfserase1953putative protein603actin 81954glycine-rich protein604hypothetical protein1955putative protein605putative protein19563-methyladenine DNA glycosylase,putative606heat-shock protein (At-1957endoplasmic reticulum-typehsc70-3)calcium-transporting ATPase 4607putative protein disulfide1958putative pectinesteraseisomerase precursor608adenosine nucleotide1959cytochrome P450-like proteintranslocator609photosystem II oxygen-evolving1960RNA-binding protein (cp33)complex protein 3-like610sedoheptulose-bisphosphatase1961CONSTANS-like 1precursor611glutathione S-transferase (GST6)1962putative small heat shock protein612geranylgeranyl reductase1963hypothetical protein613hypothetical protein1964unknown protein614hypothetical protein1965cytochrome P450-like protein615phosphoribulokinase precursor1966cysteine proteinase inhibitor likeprotein616high mobility group protein1967nicotianamine synthase(HMG1), putative(dbj|BAA74589.1)617protease inhibitor II1968copper amine oxidase like protein(fragment2)618protease inhibitor II1969putative SCARECROW generegulator619cytochrome P450 90A11970unknown protein(sp|Q42569)620unknown protein1971unknown protein621heat shock protein 901972putative alanine acetyltransferase622tubulin beta-9 chain1973unknown protein623putative ubiquitin carboxyl1974unknown proteinterminal hydrolase624protein kinase1975unknown protein625DRE/CRT-binding protein1976putative extensinDREB1C626histidyl-tRNA synthetase1977putative protein kinase627splicing factor, putative1978putative protein kinase628glutamyl-tRNA synthetase1979NADPH-dependentcodeinone reductase,putative629putative RING zinc finger protein1980peroxidase630phytochelatin synthase1981putative cytochrome P450(gb|AAD41794.1)631putative C2H2-type zinc finger1982No function assigned byproteinTIGR632putative ligand-gated ion channel1983putative zinc-finger proteinprotein(B-box zinc finger domain)633putative ribosomal-protein S61984putative tyrosinekinase (ATPK6)aminotransferase634MOLYBDOPTERIN1985hypothetical proteinBIOSYNTHESIS CNX1PROTEIN635temperature-sensitive omega-31986DNA binding proteinfatty acid desaturase, chloroplastprecursor (sp|P48622)636adenylosuccinate synthetase1987putative fatty acid elongase637putative 14-3-3 protein1988bZIP transcription factor-like protein638putative cytochrome P4501989xyloglucanfucosyltransferase, putative639putative two-component1990unknown proteinresponse regulator 3 protein640putative RING-H2 zinc1991unknown proteinfinger protein ATL6641No function assigned by1992putative proteinTIGR642small zinc finger-like1993myb factor, putativeprotein643hypothetical protein1994Myb-family transcriptionfactor, putative644MAP kinase (ATMPK6)1995putative fructosebisphosphate aldolase645vacuolar ATP synthase,1996myrosinase-associatedputativeprotein, putative646kinesin-like protein1997cytochrome P450 likeprotein647serine/threonine-specific1998similar to SOR1 from theprotein kinase NAKfungus Cercosporanicotianae648No function assigned by1999similar to embryo-abundantTIGRprotein GB:L47672 GI:1350530[ Picea glauca ]649ACTIN 2/7 (sp|P53492)2000alcohol dehydrogenase650phosphoglycerate kinase,2001auxin response factor 1putative651homeotic protein BEL12002pathogenesis-related protein 1homologprecursor, 18.9K652proline iminopeptidase2003hypothetical protein653pasticcino 12004unknown protein654serine/threonine protein2005zinc finger protein Zat12kinase655cytochrome P4502006unknown proteinmonooxygenase(CYP71B4)656No function assigned by2007unknown proteinTIGR657putative GDSL-motif2008cyclin, putativelipase/hydrolase658putative protein20092-dehydro-3-deoxyphosphoheptonate aldolase659unknown protein2010glutathione synthetase gsh2660hypothetical protein2011heat shock protein 17661putative glycosylation2012putative Na+-dependent inorganicenzymephosphate cotransporter662No function assigned by2013No function assigned by TIGRTIGR663No function assigned by2014unknown proteinTIGR664unknown protein2015putative protein665putative ABC transporter2016similar to RING-H2 finger proteinRHC1a GB:AAC69854GI:3790583 from [ Arabidopsisthaliana ]666nifU-like protein2017calcium-binding protein-like667putative receptor-like protein2018putative proteinkinase668putative disease resistance protein2019putative aldehyde dehydrogenase669receptor-like protein kinase-like2020auxin-responsive GH3-likeprotein670ubiquitin activating enzyme 22021putative protein(gb|AAB37569.1)671No function assigned by TIGR2022Phosphoglycerate dehydrogenase-like protein672putative receptor-like protein2023unknown proteinkinase673K+ transporter, AKT12024unknown protein674shaggy-like kinase beta2025PSI type III chlorophyll a/b-binding protein, putative675heat shock protein 702026putative protein676plasma membrane intrinsic protein2027putative protein1a677HSP90-like protein2028glutaredoxin, putative678histone H1, putative2029hypothetical protein679unknown protein2030No function assigned by TIGR680dnaK-type molecular chaperone2031putative proteinhsc70.1-like681gamma-glutamylcysteine2032jasmonate inducible protein,synthetaseputative682peroxidase (ATP22a)2033putative polygalacuronaseisoenzyme 1 beta subunit683putative serine carboxypeptidase2034putative small heat shock proteinprecursor684putative dioxygenase2035unknown protein685glucose transporter2036putative disease resistanceprotein686NOI protein, nitrate-induced2037putative protein687putative protein2038ethylene-responsiveelement binding factor,putative688putative protein2039putative protein689unknown protein2040Pollen-specific proteinprecursor like690putative photosystem I reaction2041putative proteincenter subunit II precursor691putative protein2042unknown protein692unknown protein2043EF-Hand containing protein-like693cobalamin biosynthesis protein2044unknown protein694adenine nucleotide translocase2045puative calcium-transporting ATPase695glutathione transferase, putative2046antifungal protein-like(PDF1.2)696putative 60S ribosomal protein L212047pathogenesis-related PR-1-like protein697cytochrome P450 like protein2048similar to Mlo proteinsfrom H. vulgare698cytochrome b245 beta chain2049putative steroidhomolog RbohAp108, putativesulfotransferase699RNA helicase, DRH12050trehalase-like protein700putative aldolase2051thioredoxin f1701farnesyltransferase subunit A2052unknown protein(FTA)702No function assigned by2053alanine-glyoxylateTIGRaminotransferase703putative putative sister-2054integral membrane protein,chromatide cohesionputativeprotein704calcium-dependent protein2055hypothetical proteinkinase705serine/threonine protein2056unknown proteinphosphatase type 2A,putative70640S ribosomal protein S282057hypothetical protein(sp|P34789)707RNA polymerase subunit2058unknown protein708DNA-damage-2059unknown proteinrepair/toleration proteinDRT102709putative C2H2-type zinc2060unknown proteinfinger protein710putative adenosine2061drought-induced-19-like 1phosphosulfate kinase711lipase2062unknown protein712putative violaxanthin de-2063putative proteinepoxidase precursor(U44133)713aromatic rich glycoprotein,2064putative proteinputative714putative fumarase2065AIG2-like protein715flavonol synthase (FLS)2066Lhca2 protein(sp|Q96330)716response regulator 5,2067phytocyaninputative717sulfate transporter2068putative chlorophyll A-B bindingprotein718putative floral homeotic2069Lhcb3 chlorophyll a/b bindingprotein, AGL9protein (gb|AAD28773.1)719putative ethylene-inducible2070luminal binding proteinprotein(dbj|BAA13948.1)720C-8,7 sterol isomerase2071hydroxypyruvate reductase (HPR)721TCH4 protein2072epoxide hydrolase (ATsEH)(gb|AAA92363.1)722hypothetical protein2073putative protein (fragment)723putative urease accessory2074unknown proteinprotein724molybdopterin synthase2075hypothetical proteinsulphurylase(gb|AAD18050.1)725putative protein2076putative glucosyl transferase726NBD-like protein2077putative glucosyl transferase(gb|AAD20643.1)727AtHVA22c2078putative 3-methylcrotonyl-CoAcarboxylase728unknown protein2079putative peroxidase729phytoene synthase2080acyl-CoA oxidase(gb|AAB65697.1)(gb|AAC13497.1)730protein kinase (AME2/AFC1)2081alternative oxidase 1a precursor731hypothetical protein2082putative transcription factor(MYB4)732cyclin-dependent protein kinase-2083serine acetyltransferaselike protein733photosystem II stability/assembly2084ATP-sulfurylasefactor HCF136 (sp|O82660)734hypothetical protein2085calreticulin (crt1)735DNA binding-like protein2086putative prohibitin 2736putative protein2087putative monodehydroascorbatereductase737chorismate mutase2088branched-chain alpha-keto aciddecarboxylase E1 beta subunit738putative LRR receptor protein2089cytokinin oxidase-like proteinkinase739putative chalcone synthase2090putative receptor-like proteinkinase740putative protein kinase2091unknown protein741replicase, putative2092hypothetical protein742putative cysteine proteinase2093No function assigned by TIGR74360S ribosomal protein L362094putative APG protein744unknown protein2095glutathione S-transferase, putative745CLC-b chloride channel protein2096phytochrome-associated protein 1(PAP1)746putative ribosomal protein S142097amidophosphoribosyltransferase747histone H2B like protein2098nonphototropic hypocotyl 1(emb|CAA69025.1)74860S ribosomal protein L220993-keto-acyl-CoA thiolase 2(gb|AAC17877.1)74960S ribosomal protein L152100pEARLI 1homolog750ribosomal protein S272101glutathione reductase, cytosolic751ribosomal protein2102putative protein75260S ribosomal protein L122103putative protein75360s ribosomal protein L342104putative aldehyde oxidase754putative ribosomal protein S102105probable photosystem Ichain XI precursor755drought-induced protein like2106photosystem II polypeptide,putative756blue copper-binding protein, 15K2107photosystem II reaction(lamin)center 6.1 KD protein757calmodulin-like protein210833 kDa polypeptide ofoxygen-evolving complex(OEC) in photosystem II(emb|CAA75629.1)758putative protein210960S ribosomal proteinL11B759No function assigned by TIGR2110extA (emb|CAA47807.1)760alpha-mannosidase, putative2111zinc finger protein OBP4-like761uncoupling protein (ucp/PUMP)2112sterol delta7 reductase762homeodomain-like protein2113putative RAS-relatedprotein, RAB11C763ribosomal protein S18,2114glucosyltransferase likeputativeprotein764similar to SOR1 from the2115zinc finger protein (PMZ),fungus Cercosporaputativenicotianae76560S ribosomal protein L13,21166,7-dimethyl-8-BBC1 proteinribityllumazine synthaseprecursor76650S ribosomal protein L24,2117putative proteinchloroplast precursor767putative ribosomal protein2118osmotin precursor768unknown protein2119No function assigned byTIGR769aspartate aminotransferase2120ferredoxin precusor isolog(AAT1)770potassium channel protein2121GH3 like proteinAtKC771unknown protein2122non-specific lipid transferprotein772peroxisomal targeting2123homeodomain transcriptionsignal type 2 receptorfactor (HAT9)773putative protein2124putative cytochrome P450monooxygenase774Ras-related GTP-binding2125putative protein kinaseprotein (ARA-4)775S-receptor kinase homolog2126putative protein2 precursor776pathogenesis-related group2127glyceraldehyde-3-5 protein, putativephosphate dehydrogenase777Nitrilase 4 (sp|P46011)2128putative protein disulfide-isomerase778biotin carboxyl carrier2129unknown proteinprotein of acetyl-CoAcarboxylase precursor(BCCP) (sp|Q42533)779photosystem I reaction2130beta-1,3-glucanase class Icentre subunit psaNprecursorprecursor (PSI-N)(sp|P49107)7803(2),5-bisphosphate2131homeobox-leucine zipper proteinnucleotidaseHAT5 (HD-ZIP protein 5) (HD-ZIP protein ATHB-1)781high affinity Ca2+2132putative cyclic nucleotide-antiporterregulated ion channel protein782putative cytoskeletal2133P II nitrogen sensing protein GLB Iprotein783putative peroxidase2134H-protein promoter binding factor-1 (gb|AAC24592.1)784respiratory burst oxidase2135GAST1-like proteinprotein785beta-glucosidase2136cytochrome P450 GA3786calcium-dependent protein kinase2137putative protein(pir||S71196)787phosphoinositide specific2138Myb-related transcription factor-phospholipase Clike protein788similarity to S-domain receptor-2139putative phloem-specific lectinlike protein kinase, Zea mays789mitosis-specific cyclin 1b2140protein kinase-like protein7904-coumarate:CoA ligase 32141unknown protein791transcription factor IIB (TFIIB)2142SCARECROW transcriptionalregulator-like792unknown protein2143unknown protein793hypothetical protein2144unknown protein794hypothetical protein2145putative protein795sugar transporter like protein2146calnexin homolog796putative trypsin inhibitor2147PP1/PP2A phosphatasespleiotropic regulator PRL2797unknown protein2148xyloglucan endotransglycosylase,putative798putative multispanning membrane2149putative calmodulinprotein799receptor-like kinase, putative2150spermine synthase (ACL5)800putative inosine-5-monophosphate2151snoRNAdehydrogenase801inosine-5′-monophosphate2152photosystem I subunit V precursor,dehydrogenase, putativeputative802amino acid permease 62153putative potassium transporter(emb|CAA65051.1)803NADPH-ferrihemoprotein2154Homeodomain-like proteinreductase (ATR2)804putative WRKY-type DNA binding2155putative proteinprotein805putative ankyrin2156unknown protein806putative hexose transporter2157CALMODULIN-RELATEDPROTEIN 2, TOUCH-INDUCED(TCH2)807aquaporin/MIP-like protein2158putative protein phosphatase 2C808Ser/Thr protein kinase isolog2159monosaccharide transportprotein, STP4809pectate lyase like protein2160hypothetical protein810putative 60S ribosomal protein L172161unknown protein811putative protein2162hypothetical protein812unknown protein2163putative protein kinase813phenylalanine ammonia-lyase2164putative serine/threonineprotein kinase814putative cytochrome P4502165jasmonate induciblemonooxygenaseprotein, putative815ARR1 protein, putative2166similar to several smallproteins (~100 aa) that areinduced by heat, auxin,ethylene and woundingsuch as Phaseolus aureusindole-3-acetic acidinduced protein ARG(SW: 32292)816putative bHLH transcription factor2167unknown protein817aminomethyltransferase-like2168MYB-like proteinprecursor protein818purple acid phosphatase precursor2169putative protein kinase819AP2 domain containing2170unknown proteinprotein, putative820ubiquitin-conjugating2171CLC-d chloride channelenzyme E2-21 kD 1protein(ubiquitin-protein ligase 4)(ubiquitin carrier protein 4)(sp|P42748)821translation initiation factor2172cytochrome P450-likeprotein822putative VAMP-associated2173putative glutathione S-proteintransferase823spermidine synthase,2174putative mandelonitrileputativelyase824putative protein2175hypothetical protein825unknown protein2176putative trypsin inhibitor826AtKAP alpha2177male sterility 2-like protein(emb|CAA68191.1)827glyceraldehyde-3-2178unknown proteinphosphate dehydrogenase,putative828putative poly(A) binding2179unknown proteinprotein829alpha-tubulin, putative2180putative protein830serine/threonine-specific2181putative peroxidaseprotein kinase ATPK64(pir||S20918)831putative aspartate-tRNA2182putative thromboxane-Aligasesynthase832ras-related small GTP-2183putative cytochrome P450binding protein RAB1c833cycloartenol synthase2184peroxidase ATP21a834No function assigned by2185unknown proteinTIGR835cytochrome P4502186putative glutathione S-transferase836GTPase AtRAB82187defender against cell death protein8373-phosphoserine2188AP2 domain containing protein,phosphataseputative838transcription factor CRC2189actin depolymerizing factor-likeprotein839nuclear cap-binding2190putative calcium-dependent proteinprotein; CBP20kinase (U90439)(gb|AAD29697.1)840chloroplast membrane2191phosphoribosylanthranilateprotein (ALBINO3)transferase, putative841biotin holocarboxylase2192oligopeptide transporter, putativesynthetase842expansin AtEx62193calmodulin-like protein843unknown protein2194putative protease inhibitor844mercaptopyruvate2195MAP kinasesulfurtransferase, putative845putative thiosulfate2196DNA binding protein MybSt1,sulfurtransferaseputative846dihydrolipoamide S-2197putative proteinacetyltransferase847auxin transport protein REH1,2198putative proteinputative848putative auxin transport protein2199unknown protein849apyrase (Atapy1)2200unknown protein850root cap 1 (RCP1)2201unknown protein851hypothetical protein2202putative protein852putative protein2203unknown protein853predicted protein of unknown2204unknown proteinfunction854hypothetical protein2205hypothetical protein855hypothetical protein2206uncharacterized protein856hypothetical protein2207putative protein857putative aldehyde dehydrogenase2208hypothetical protein858putative peroxidase2209peroxidase (emb|CAA66967.1)859UDP-glucose 4-epimerase-like2210putative flavonol 3-O-proteinglucosyltransferase860indole-3-acetate beta-2211putative flavonol 3-O-glucosyltransferase like proteinglucosyltransferase861putative beta-1,3-glucanase2212putative protein862disease resistance protein-like2213glycerol-3-phosphateacyltransferase863putative respiratory burst oxidase2214putative beta-1,3-glucanaseprotein B864ubiquitin-conjugating enzyme2215putative ethylene response elementUBC3binding protein (EREBP)865cytoplasmic aconitate hydratase2216putative CONSTANS-like B-boxzinc finger protein866NADPH oxidoreductase, putative2217putative protein867PROTEIN TRANSPORT2218unknown proteinPROTEIN SEC61 GAMMASUBUNIT-like868putative protein2219putative trehalose-6-phosphatephosphatase (AtTPPA)869unknown protein2220putative protein87060S acidic ribosomal protein P22221putative protein871No function assigned by TIGR2222unknown protein8721,4-alpha-glucan branching2223unknown prpteinenzyme protein soform SBE2.2precursor873calcium binding protein (CaBP-22)2224unknown protein874putative phosphoglucomutase2225hypothetical protein875shaggy-like protein kinase2226putative metal-bindingetha (EC 2.7.1.-)protein876pyruvate decarboxylase2227putative(gb|AAB16855.1)phosphoribosylglycinamidesynthetase877hypothetical protein2228unknown protein878putative protein kinase2229putative protein879putative protein kinase2230unknown protein880putative leucine2231unknown proteinaminopeptidase881probable cytochrome P4502232putative beta-galactosidase882protein kinase 6-like protein2233putative protein kinase883arginine methyltransferase2234putative protein(pam1)884MYB96 transcription2235putative proteinfactor-like proteinphosphatase 2C885putative protein2236putative growth regulatorprotein886metal ion transporter2237putative ABC transporter887No function assigned by2238chloride channelTIGR(emb|CAA70310.1)888flax rust resistance protein,2239adrenodoxin-like proteinputative889fructose-2,6-2240NAM (no apical meristem)-bisphosphatase, putativelike protein890exonuclease RRP412241putative transcription factorMYB41891squamosa promoter binding2242Myb DNA binding protein-protein-like 2like(emb|CAB56576.1)892putative squamosa-2243AtMYB84promoter binding protein893O-acetylserine (thiol) lyase,2244photosystem II type Iputativechlorophyll a/b bindingprotein894snoRNA2245putative aspartic proteinase895snoRNA2246jasmonate inducibleprotein, putative896ferredoxin-NADP+2247putative proteinreductase897H+-transporting ATP2248No function assigned bysynthase chain 9-likeTIGRprotein898photosystem I subunit III2249putative phosphatidylserineprecursor, putativesynthase899photosystem I subunit VI2250putative nicotianamineprecursorsynthase900auxin-binding protein 12251lysine and histidine specificprecursortransporter, putative901putative RAS superfamily GTP-2252putative proteinbinding protein902disease resistance protein-like2253putative protein903protein kinase like protein2254putative sugar transporter protein904glucuronosyl transferase-like225512S cruciferin seed storage proteinprotein905putative homeodomain2256putative auxin-induced protein,transcription factorIAA17/AXR3-1906putative flavonol reductase2257putative cyclin D907putative protein2258farnesyl diphosphate synthaseprecursor (gb|AAB49290.1)908salt-tolerance protein2259putative potassium transportprotein (TRH1)90940S ribosomal protein S302260putative NPK1-related MAP kinase910putative bZIP transcription factor2261putative protein911putative protein2262putative ABC transporter912putative cinnamoyl CoA reductase2263putative DNA-directed RNApolymerase subunit913unknown protein2264putative small nuclearribonucleoprotein E914putative RNA-binding protein2265unknown protein915phosphatidylinositol synthase2266reticuline oxidase-like protein(PIS1)916unknown protein2267putative 1-aminocyclopropane-1-carboxylate oxidase917hydroxyproline-rich glycoprotein2268similar to Mlo proteins from H.homologvulgare91850S ribosomal protein L15,2269long-chain-fatty-acid—CoA ligase-chloroplast precursorlike protein919unknown protein2270putative protein920putative YME1 ATP-dependant2271chromatin remodelling complexproteaseATPase chain ISWI-like protein921unknown protein2272hypothetical protein922putative ribosomal protein L282273latex-abundant protein, putative923unknown protein2274N-acetylornithine deacetylase-likeprotein, fragment924putative protein2275putative DNA-binding protein925protein ch-42 precursor,2276putative anthranilate N-chloroplasthydroxycinnamoyl/benzoyltransferase926protein serine/threonine kinase,2277putative DNA binding proteinputative927beta-VPE2278cytochrome P450-like protein928putative vacuolar sorting receptor2279putative DNA-binding protein929putative translation initiation factor2280putative peptide transporterIF-2930predicted protein of unknown2281putative reticuline oxidase-likefunctionprotein931putative protein2282thioredoxin, putative932hypothetical protein2283nodulin-like protein933hypothetical protein2284UDP-galactose transporter-like protein934phosphate transporter, putative2285putative fibrillin935No function assigned by2286unknown proteinTIGR936beta subunit of protein2287unknown proteinfarnesyl transferase ERA1937putative glutamate2288unknown proteindecarboxylase938putative indole-3-acetate2289hypothetical proteinbeta-glucosyltransferase939putative receptor-like2290glyceraldehyde 3-phosphateprotein kinasedehydrogenase A subunit(GapA)940UDP-galactose 4-2291predicted protein ofepimerase-like proteinunknown function941putative proliferating cell2292putative proteinnuclear antigen, PCNA942ubiquitin conjugating2293putative proteinenzyme E2 (UBC13)943cyclophilin (CYP2)2294myb-like protein944cystatin2295hypothetical protein(emb|CAA03929.1)945putative alcohol2296putative U5 small nucleardehydrogenaseribonucleoprotein, an RNAhelicase946acidic ribosomal protein p12297unknown protein947glutathione transferase2298cinnamyl alcoholAtGST 10dehydrogenase-like(emb|CAA10457.1)protein948putative tropinone2299hypothetical protein similarreductaseto extensin-like protein949ZIP4, a putative zinc2300unknown proteintransporter950unknown protein2301putative chlorophyll a/bbinding protein951putative protein2302probable plasma membraneintrinsic protein 1c952putative protein2303hexokinase (ATHXK2)953putative C2H2-type zinc2304calcium-dependent proteinfinger proteinkinase954putative RING zinc finger23055′-adenylylphosphosulfateproteinreductase, putative955putative microtubule-2306Erd1 protein precursorassociated protein(sp|P42762)956unknown protein2307putative protein957putative protein2308putative protein958putative protein2309unknown proteinphosphatase-2c959V-ATPase subunit G (vag22310BCS1 protein-like proteingene)960hypothetical protein2311putative protein961unknown protein2312putative protein962unknown protein2313putative protein kinase963unknown protein2314indoleacetic acid (IAA)-induciblegene (IAA7)964myrosinase-associated protein,2315ATP-dependent Clp proteaseputativeregulatory subunit CLPX965hypothetical protein2316DNA-binding protein RAV1966hypothetical protein2317putative protein967No function assigned by TIGR2318hypothetical protein968unknown protein2319unknown protein969hypothetical protein2320unknown protein970LAX1/AUX1-like permease2321putative protein971putative UDP-N-2322putative thioredoxin reductaseacetylglucosamine--dolichyl-phosphate N-acetylglucosaminephosphotransferase972chorismate mutase CM22323unknown protein973inner mitochondrial membrane2324putative lectinprotein974DEF (CLA1) protein2325No function assigned by TIGR975decoy2326beta-fructosidase976citrate synthase2327chlorophyll a/b-binding proteinCP29977myosin2328photosystem I subunit PSI-E-likeprotein97840S ribosomal protein S192329peroxidase ATP8a979ripening-related protein-like2330putative fructose bisphosphatealdolase980putative signal peptidase I2331zinc finger protein ATZF1,putative981methionyl-tRNA synthetase2332DegP protease precursor(AtcpMetRS)982ribosomal protein precursor-like2333transcription factor-like protein98350S ribosomal protein L212334calcium-dependent protein kinasechloroplast precursor (CL21)984putative MYB family transcription2335hypothetical proteinfactor985cyclophilin-like protein2336putative protein986hypothetical protein2337glucose-1-phosphateadenylyltransferase (APL3)987naringenin 3-dioxygenase like2338No function assigned by TIGRprotein988WD-repeat protein-like protein2339putative Eukaryotic initiation factor4A989putative serine carboxypeptidase II2340No function assigned by TIGR990prenyltransferase, putative2341unknown protein991putative ligand-gated ion channel2342beta tubulin 1, putativeprotein992clathrin adaptor medium chain2343one helix protein (OHP)protein MU1B, putative993No function assigned by TIGR2344No function assigned by TIGR994putative Tal 1-like non-2345zinc finger protein 5, ZFP5LTR retroelement protein995putative 3-isopropylmalate2346putative MYB family transcriptiondehydrogenasefactor9963-isopropylmalate2347putative amino acid transporterdehydratase, small subunitprotein997unknown protein2348putative potassiumtransporter998unknown protein2349protein kinase (AFC2)999unknown protein2350putative protein1000hypothetical protein2351No function assigned byTIGR1001putative protein2352putative ubiquitin-conjugating enzyme E21002No function assigned by2353unknown proteinTIGR1003putative beta-glucosidase2354cytochrome P450monooxygenase (CYP71B3)1004putative pectate lyase A112355putative myrosinase-binding protein1005putative beta-glucosidase2356putative vacuolar sortingreceptor1006HD-Zip protein2357uridine diphosphate glucoseepimerase1007putative ubiquitin2358shaggy related proteinconjugating enzymekinase, ASK-GAMMA1008homeobox-leucine zipper2359ankyrin repeat proteinprotein-likeEMB5061009cytochrome P450 like2360putative beta-alanine-proteinpyruvate aminotransferase1010putative cysteine proteinase2361putative alcoholinhibitor B (cystatin B)dehydrogenase1011ethylene response sensor2362putative receptor-like(ERS)protein kinase1012putative SWH1 protein2363unknown protein1013putative glutathione S-2364putative methylmalonatetransferasesemi-aldehydedehydrogenase1014putative protein2365hypothetical protein1015unknown protein2366unknown protein1016putative protein2367peroxidase ATP13aphosphatase 2C1017dnaJ protein homolog atj32368putative glutathioneperoxidase1018ferredoxin2369squamosa promoter bindingprotein-like 71019hypothetical protein2370photosystem II corecomplex protein, putative1020putative sugar transport2371snoRNAprotein, ERD61021putative DnaJ protein2372photosystem I subunit Xprecursor1022putative AP2 domain2373MYB transcription factortranscription factor(Atmyb2)1023putative protein2374putative PHD-type zinc fingerprotein1024putative cyclin-dependent2375nuclear RNA binding protein A-kinase regulatory subunitlike protein1025putative tropinone reductase2376unknown protein1026signal response protein (GAI)2377unknown protein1027putative steroid sulfotransferase2378unknown protein1028hypothetical protein2379putative amino-cyclopropane-carboxylic acid oxidase (ACCoxidase)1029nucleic acid binding protein-like2380hypothetical protein1030putative protein2381indole-3-acetate beta-glucosyltransferase like protein1031blue copper binding protein2382predicted protein1032farnesylated protein (ATFP6)2383unknown protein1033unknown protein2384No function assigned by TIGR1034putative PCF2-like DNA binding2385putative photosystem I reactionproteincenter subunit IV1035teosinte branched1-like protein2386putative homeodomaintranscription factor1036putative protein2387putative purple acid phosphataseprecursor1037unknown protein2388No function assigned by TIGR1038unknown protein2389nitrate reductase 1 (NR1)10392-oxoglutarate dehydrogenase, E12390putative casein kinase II betacomponentsubunit1040unknown protein2391pEARLI 1-like protein1041unknown protein2392putative protein1042CCAAT-binding transcription2393No function assigned by TIGRfactor subunit A (CBF-A)1043hypothetical protein2394unknown protein1044putative growth regulator protein2395putative cell wall-plasmamembrane disconnecting CLCTprotein (AIR1A)1045putative presenilin2396unknown protein1046putative expansin2397scarecrow-like 11-like1047ribosomal-like protein2398putative anthocyanidin synthase1048unknown protein2399putative AP2 domain transcriptionfactor1049unknown protein2400caffeoyl-CoA O-methyltransferase-like protein1050putative protein2401unknown protein1051putative protein2402putative protein kinase1052unknown protein2403cytochrome P450-like protein1053unknown protein2404putative MADS-box protein ANR11054unknown protein2405putative glutathione S-transferase1055unknown protein2406hypothetical protein1056unknown protein2407similar to gibberellin-regulated proteins1057putative protein2408unknown protein1058putative protein2409putative sensorytransduction histidinekinase1059argininosuccinate lyase (AtArgH)2410similar to lateembryogenesis abundantproteins1060disease resistance protein homolog2411unknown protein1061aldehyde dehydrogenase like2412putative proteinprotein1062GBF2, G-box binding factor2413putative ATP-dependentRNA helicase1063CDPK-related kinase2414putative protein1064endo-1,4-beta-glucanase2415putative sucrose synthetase1065putative serine protease2416beta-fructofuranosidase 11066serine/threonine-specific2417putative indole-3-acetatekinase lecRK1 precursor, lectinbeta-glucosyltransferasereceptor-like1067putative MAP kinase2418hypothetical protein1068RNase L inhibitor-like2419DNA-directed RNAproteinpolymerase II, third largest subunit1069No function assigned by2420putative transcription factorTIGR1070AP2 domain transcription2421homeobox-leucine zipperfactorprotein ATHB-5 (HD-zip proteinATHB-5) (sp|P46667)1071polygalacturonase2422putative ftsH chloroplastisoenzyme 1 beta subunit,proteaseputative1072putative lipid transfer2423replication protein A1-likeprotein1073putative protein kinase2424hypothetical protein1074putative protein2425unknown protein1075ATP-dependent RNA2426unknown proteinhelicase like protein1076putative cyclic nucleotide-2427putative methionineregulated ion channelaminopeptidaseprotein1077COP1 like protein2428unknown protein1078putative peroxidase2429fatty acid elongase-likeprotein (cer2-like)1079putative NAK-like ser/thr2430unknown proteinprotein kinase1080putative cytochrome C2431putative disease resistanceresponse protein1081cytochrome c2432putative protein1082putative serine2433unknown proteincarboxypeptidase II1083acyl-(acyl carrier protein)2434putative proteinthioesterase1084DNA-binding factor,2435putative proteinputative1085MAP3K delta-1 protein2436unknown proteinkinase1086AtMlo-h1-like protein2437putative protein1087No function assigned by2438unknown proteinTIGR1088putative expansin2439unknown protein1089defender against cell death2440putative proteinprotein, putative1090glycolate oxidase-like2441No function assigned by TIGRprotein1091putative ATP-dependent RNA2442MADS-box protein AGL14helicase1092putative protein2443No function assigned by TIGR1093putative HMG protein2444peptidylprolyl isomerase1094squalene monooxygenase 22445putative s-adenosylmethionine(squalene epoxidase 2) (SE 2)synthetase(sp|O65403)1095eukaryotic peptide chain release2446peroxidasefactor subunit 1, putative1096auxin-induced protein-like2447ferrochelatase-I1097putative lipoamide dehydrogenase2448putative eukaryotic initiation factor4, eIF41098putative protein2449drought-inducible cysteineproteinase RD21A precursor-likeprotein1099unknown protein2450unknown protein1100putative oligopeptide transporter2451unknown protein1101putative translation elongation2452No function assigned by TIGRfactor ts1102putative CCAAT-binding2453No function assigned by TIGRtranscription factor subunit1103putative ABC transporter2454salt-inducible like protein1104putative superoxide-generating2455glucose-6-phosphate 1-NADPH oxidase flavocytochromedehydrogenase1105aspartate kinase-homoserine24563-hydroxy-3-methylglutaryl CoAdehydrogenase-like proteinreductase (AA 1-592)1106putative bHLH transcription factor2457hypothetical protein1107putative geranylgeranyl transferase2458putative proteintype I beta subunit1108putative ARP2/3 protein complex2459putative putative 60S ribosomalsubunit p41protein L171109sulphite reductase2460putative inorganic pyrophosphatase1110putative auxin-regulated protein2461putative gamma-glutamyltransferase1111transcription factor scarecrow-like2462heat shock transcription factor-14, putativelike protein1112unknown protein2463mitochondrial chaperonin hsp601113monooxygenase 2 (MO2)2464unknown protein1114putative amine oxidase2465putative zinc finger proteinidentical to T10M13.221115zinc finger protein, putative2466putative uridylyl transferase1116DNA-binding protein, putative2467nodulin-like protein1117putative protein2468putative B-box zinc finger protein1118putative protein2469No function assigned by TIGR1119Avr9 elicitor response like protein2470putative metalloproteinase1120putative protein2471putative cellular apoptosissusceptibility protein1121hypothetical protein2472hypothetical protein1122putative nucleotide-sugar2473hypothetical proteindehydratase1123UFD1 like protein2474scarecrow-like 13 (SCL13)1124putative trans-2475putative nucleosideprenyltransferasetriphosphatase1125outward rectifying2476unknown proteinpotassium channel KCO1126unknown protein2477No function assigned byTIGR1127putative2478hypothetical proteinpectinacetylesterase1128putative protein2479putative phospholipase1129No function assigned by2480putative snRNP proteinTIGR1130unknown protein2481putative protein1131unknown protein2482putative lipase1132unknown protein2483putative nonsense-mediatedmRNA decay protein1133protein phosphatase2484No function assigned byhomolog (PPH1)TIGR1134unknown protein2485protochlorophyllidereductase precursor1135No function assigned by2486No function assigned byTIGRTIGR1136unknown protein2487trehalose-6-phosphatesynthase, putative1137unknown protein2488unknown protein1138unknown protein2489germin-like protein1139putative protein2490plastid protein1140unknown protein2491putative protein1141putative ubiquinol--2492hypothetical proteincytochrome-c reductase1142unknown protein2493unknown protein1143contains similarity to high-2494unknown proteinglucose-regulated protein 8GB:AAF08813 GI:6449083from [ Homo sapiens ]1144unknown protein2495histone deacetylase-likeprotein1145putative cis-Golgi SNARE2496unknown proteinprotein1146unknown protein2497unknown protein1147glutamate-1-semialdehyde2498putative proteinaminotransferase1148No function assigned by2499putative proteinTIGR1149hypothetical protein2500No function assigned byTIGR1150unknown protein2501putative zinc transporterZIP2-like1151unknown protein2502unknown protein1152unknown protein2503putative ribosomal-proteinS6 kinase (ATPK19)1153scarecrow-like 32504unknown protein1154putative proline-rich protein2505unknown protein1155cytochrome c oxidoreductase like250660S ribosomal protein L10Aprotein1156putative2507putative proteincarboxymethylenebutenolidase1157unknown protein2508receptor protein kinase (IRK1),putative1158unknown protein2509putative nematode-resistanceprotein1159unknown protein2510tubulin alpha-5 chain-like protein1160unknown protein2511putative DNA-binding protein1161unknown protein2512unknown protein1162unknown protein2513putative RGA1, giberellin repsonsemodulation protein1163auxin-induced protein (IAA20)2514non phototropic hypocotyl 1-like116450S ribosomal protein L42515RING-H2 finger protein RHA1b1165putative DNA topoisomerase III2516putative myb-proteinbeta1166No function assigned by TIGR2517hydroperoxide lyase (HPOL) likeprotein1167isp4 like protein2518serine/threonine-protein kinase,PK71168putative protein kinase2519putative vacuolar proton-ATPasesubunit1169hypothetical protein2520putative polygalacturonase1170putative pyrophosphate--fructose-2521putative ribosomal protein L86-phosphate 1-phosphotransferase1171putative protein2522putative adenylate kinase1172putative protein2523germin-like protein (GLP10)1173putative protein2524putative chlorophyll a/b bindingprotein1174unknown protein2525chloroplast single subunit DNA-dependent RNA polymerase1175unknown protein2526putative protein1176putative protein2527hypothetical protein1177putative protein2528hypothetical protein1178unknown protein2529b-keto acyl reductase, putative1179unknown protein2530cellulose synthase catalytic subunit1180putative protein2531putative 1-aminocyclopropane-1-carboxylate oxidase1181brassinosteroid insensitive 1 gene2532S-linalool synthase, putative(BRI1)1182putative receptor protein kinase2533phosphoribosyl-ATPpyrophosphohydrolase (At-IE)1183vacuolar-type H+-translocating2534disease resistance RPP5 likeinorganic pyrophosphataseprotein (fragment)1184protein kinase-like protein2535putative protein1185glycyl tRNA synthetase, putative2536beta-galactosidase like protein1186subtilisin proteinase-like2537putative translationinitiation factor eIF-2,gamma subunit1187hypothetical protein2538ankyrin like protein1188cytochrome P450-like protein2539histone H2A-like protein1189cytochrome p450 like protein2540putative protein1190putative protein kinase2541salt-tolerance zinc fingerprotein1191pectinesterase-like protein2542unknown protein1192putative receptor-like protein2543putative proteinkinase1193peroxidase ATP17a-like2544fructose-bisphosphateproteinaldolase1194No function assigned by2545peroxidaseTIGR(emb|CAA66964.1)1195cellulose synthase catalytic2546patatin-like proteinsubunit-like protein1196RAS-related protein, RAB72547salt-inducible proteinhomolog1197putative aspartate2548hypothetical proteinaminotransferase1198cyclophilin2549xyloglucan endo-transglycosylase-likeprotein1199putative SF2/ASF splicing2550trihelix DNA-bindingmodulator, Srp30protein (GT2)1200putative cytochrome b52551ubiquitin-conjugatingenzyme 16, putative1201glutamyl-tRNA reductase,2552homeobox proteinputative1202putative MADS-box protein2553envelope Ca2+-ATPase1203ammonium transport2554snap25aprotein (AMT1)1204No function assigned by2555putative annexinTIGR1205putative beta-ketoacyl-CoA2556putative proteinsynthase1206thaumatin-like protein2557homeodomain transcriptionfactor (ATHB-14)1207putative methionine2558heat shock protein, putativeaminopeptidase1208putative protein2559peroxidase ATP23aphosphatase 2C1209kinase-like protein2560p68 RNA helicase, putative1210receptor-associated kinase2561potassium transporter,isologputative1211mitochondrial ribosomal2562putative eukaryoticprotein S14translation initiation factor 2 alphasubunit, eIF21212oleosin, 18.5K2563hypothetical protein1213chalcone isomerase2564carnitine racemase likeprotein1214putative cyclin-dependent2565No function assigned bykinase regulatory subunitTIGR1215putative thaumatin-like2566unknown proteinprotein1216putative two-component2567unknown proteinresponse regulator protein1217TATA binding protein-2568unknown proteinassociated factor, putative1218predicted protein of2569serine/threonine kinase-likeunknown functionprotein1219putative AP2 domain transcription2570peroxidase (emb|CAA66960.1)factor1220brassinosteroid receptor kinase,2571putative proteinputative1221TINY-like protein2572hypothetical protein1222glucose-6-phosphate isomerase2573glycine-rich protein 2 (GRP2)1223putative protein2574unknown protein1224putative NAM (no apical2575berberine bridge enzyme-likemeristem)-like proteinprotein1225unknown protein2576unknown protein1226putative nucleotide-binding protein2577putative WD-repeat protein1227bZIP transcription factor (POSF21)2578serine/threonine kinase-likeprotein1228ubiquitin activating enzyme-like2579serine/threonine kinase-likeproteinprotein1229telomere repeat-binding protein2580Cu2+-transporting ATPase-likeprotein1230unknown protein2581translation initiation factor eIF4E1231mevalonate kinase2582O-methyltransferase-like protein1232putative protein2583translation initiation factor eIF3-like protein1233hypothetical protein2584No function assigned by TIGR1234disease resistance RPP5 like2585unknown proteinprotein1235putative protein2586hypothetical protein1236putative pectinesterase2587unknown protein1237Ttg1 protein (emb|CAB45372.1)2588unknown protein1238FUSCA PROTEIN FUS62589glycine-rich protein like1239NHE1 Na+/H+ exchanger2590putative disease resistance protein1240No function assigned by TIGR2591putative Na+/Ca2+ antiporter1241Phospholipase like protein2592putative hydroxymethylglutaryl-CoA lyase1242unknown protein2593putativephosphoribosylaminoimidazolecarboxylase1243unknown protein2594SAR DNA-binding protein-like1244unknown protein2595response regulator, putative1245AUX1-like amino acid permease2596fibrillin precursor-like protein1246unknown protein2597beta-ketoacyl-CoA synthase(FIDDLEHEAD)1247putative C2H2-type zinc finger2598lectin like proteinprotein1248putative protein2599No function assigned by TIGR1249putative protein2600acidic endochitinase(dbj|BAA21861.1)1250putative glucosyltransferase2601unknown protein1251putative lipase2602hypothetical protein1252putative protein2603predicted OR23 protein ofunknown function1253putative thioredoxin2604putative protein1254AIG2-like protein2605hypothetical protein1255short-chain alcohol dehydrogenase2606glycerol-3-phosphatelike proteindehydrogenase1256hypothetical protein2607hypothetical protein1257putative protein2608tat-binding protein, putative1258putative protein2609putative protein1259glutathione peroxidase-2610putative trehalose-6-like proteinphosphate phosphatase1260putative protein2611hypothetical protein1261putative disease resistance2612putative flavonol 3-O-response proteinglucosyltransferase1262putative protein261360S ribosomal protein L301263senescence-associated2614putative auxin-inducedprotein (SAG29)protein1264glycolate oxidase, putative2615putative nonspecific lipid-transfer protein precursor1265extensin-like protein2616AtRer1A1266putative protein2617putative aquaporin(tonoplast intrinsic proteingamma)1267unknown protein2618hypothetical protein1268putative disease resistance2619putative alanine acetylproteintransferase1269putative receptor-like2620putative NADP-dependentprotein kinaseglyceraldehyde-3-phosphate dehydrogenase1270putative receptor-like2621putative DNA bindingprotein kinaseprotein1271basic chitinase2622putative cystathioninegamma-synthase1272putative pectin2623unknown proteinmethylesterase1273peroxidase ATP N2624malate oxidoreductase(malic enzyme)1274class 2 non-symbiotic2625unknown proteinhemoglobin1275nitrate transporter2626cyclic nucleotide-gatedcation channel1276Ca2+/H+-exchanging2627glyoxalase II, putativeprotein-like1277putative protein2628putative trypsin inhibitor1278hydroxynitrile lyase like2629unknown proteinprotein1279putative AP2 domain2630unknown proteintranscription factor1280pectin methylesterase,2631unknown proteinputative1281putative protein2632nucleosome assembly protein I-likeprotein1282beta-glucosidase-like2633membrane channel like proteinprotein1283CCAAT box binding factor/2634anthocyanin2, putativetranscription factor Hap2a1284putative fibrillin2635TWIN SISTER OF FT (TSF)1285xyloglucan endo-2636putative myb-related transcriptiontransglycosylasefactor1286putative 10 kd chaperonin2637hypothetical protein1287No function assigned by TIGR2638putative RING zinc finger protein1288serine/threonine protein kinase2639amino acid transport protein AAT1ATPK101289putative lipase2640putative protein1290choline kinase GmCK2p-like2641putative proteinprotein1291putative sugar transport protein,2642xanthine dehydrogenaseERD61292MYB27 protein-like2643xanthine dehydrogenase-likeprotein1293DNA-binding protein, putative2644receptor protein kinase (IRK1),putative1294similar to cold acclimation protein2645dehydrin-like proteinWCOR413 [ Triticum aestivum ]1295unknown protein2646unknown protein1296aquaporin (plasma membrane2647aldehyde dehydrogenase homolog,intrinsic protein 2B)putative1297No function assigned by TIGR2648Ran binding protein (AtRanBP1b)1298P-Protein-like protein2649putative squamosa-promoterbinding protein1299No function assigned by TIGR2650putative protein1300putative cytochrome P4502651kinesin like proteinmonooxygenase1301putative cytochrome P4502652putative cellulose synthasemonooxygenase1302putative thioredoxin2653calmodulin (cam2)1303stromal ascorbate peroxidase2654fibrillarin-like protein1304ethylene responsive element2655putative transmembrane proteinbinding factor-like proteinG5p(AtERF6)1305auxin transport protein EIR12656putative peroxidase(gb|AAC39513.1)1306putative CONSTANS-like B-box2657putative SNF1-related proteinzinc finger proteinkinase1307putative protein kinase2658glutathione S-transferase, putative1308mitochondrial Lon protease2659unknown proteinhomolog 1 precursor (sp|O64948)1309putative protein2660hypothetical protein1310heme activated protein, putative2661putative protein1311putative cytochrome P4502662phosphatidylinositol-4-phosphate5-kinase isolog1312No function assigned by TIGR2663putative tyrosine decarboxylase1313putative lipase2664unknown protein1314putative protein2665SGP1 monomeric G-protein(emb|CAB54517.1)1315putative sugar transporter protein2666putative serinecarboxypeptidase II1316putative sucrose transport protein,2667putative L5 ribosomalSUC2proteiii1317putative protein2668putative glucosyltransferase1318putative protein2669flavonoid 3,5-hydroxylaselike protein1319putative endochitinase2670putative protein1320putative acetone-2671putative proteincyanohydrin lyase1321putative protein2672putative Fe (II)/ascorbateoxidase1322calmodulin-like protein2673putative anthocyanin 5-aromatic acyltransferase1323hypothetical protein2674casein kinase I1324cysteine proteinase like2675putative 2,3-proteinbisphosphoglycerate-independentphosphoglycerate mutase1325heat shock protein 17.6-II2676putative glutathione S-transferase TSI-11326heat shock protein 182677ATP-dependent RNAhelicase1327Arabidopsis mitochondrion-2678putative cytochrome P450localized small heat shockprotein (AtHSP23.6-mito)1328unknown protein2679putative WD-40 repeatprotein1329putative WRKY-type DNA2680No function assigned bybinding proteinTIGR1330No function assigned by2681No function assigned byTIGRTIGR1331hypothetical protein2682putative protein1332putative integral membrane2683putative extensinprotein nodulin1333putative protein2684nodulin-26-like protein1334unknown protein2685RNA helicase(emb|CAA09212.1)13353-isopropylmalate2686predicted protein ofdehydratase, small subunitunknown function1336unknown protein2687putative berberine bridgeenzyme1337putative homeodomain2688thioredoxin, putativetranscription factor1338unknown protein2689putative serinecarboxypeptidase I1339putative protein2690cytochrome P450-likeprotein1340peroxidase ATP19a2691putative pyrophosphate-dependentphosphofructokinase alpha subunit1341putative Na+/H+-2692putative flavonolexchanging proteinglucosyltransferase1342putative auxin-regulated2693peroxidase ATP20aprotein(emb|CAA67338.1)1343unknown protein2694TOPP8 serine/threonine proteinphosphatase type one1344unknown protein2695auxin regulated protein IAA18,putative1345putative trehalose-6-2696putative WRKY-type DNA bindingphosphate synthaseprotein1346putative lectin2697putative glucan synthase1347Mlo protein-like2698squalene monooxygenase1348unknown protein2699putative proline-rich protein1349ethylene response factor,2700G2484-1 proteinputative1350unknown protein2701heat shock protein 70 like protein1351unknown protein2702unknown protein2703unknown protein TABLE 2ABIOTIC STRESS RESPONSIVEGENE REGULATORY SEQUENCESSEQREGULATORYSEQREGULATORYID NOREGIONID NOREGION12704135340462270513544047327061355404842707135640495270813574050627091358405172710135940528271113604053927121361405410271313624055112714136340561227151364405713271613654058142717136640591527181367406016271913684061172720136940621827211370406319272213714064202723137240652127241373406622272513744067232726137540682427271376406925272813774070262729137840712727301379407228273113804073292732138140743027331382407531273413834076322735138440773327361385407834273713864079352738138740803627391388408137274013894082382741139040833927421391408440274313924085412744139340864227451394408743NONE139540884427461396408945274713974090462748139840914727491399409248275014004093492751140140945027521402409551275314034096522754140440975327551405409854275614064099552757140741005627581408410157275914094102582760141041035927611411410460276214124105612763141341066227641414410763276514154108642766141641096527671417411066276814184111672769141941126827701420411369NONE14214114702771142241157127721423411672277314244117732774142541187427751426411975277614274120762777142841217727781429412278277914304123792780143141248027811432NONE81278214334125822783143441268327841435412784278514364128852786143741298627871438413087278814394131882789144041328927901441413390279114424134912792144341359227931444413693279414454137942795144641389527961447413996279714484140972798144941419827991450414299280014514143100280114524144101280214534145102280314544146103280414554147104280514564148105280614574149106280714584150107280814594151108280914604152109281014614153110281114624154111281214634155112281314644156113281414654157114281514664158115281614674159116281714684160117281814694161118281914704162119282014714163120282114724164121282214734165122282314744166123282414754167124282514764168125282614774169126282714784170127282814794171128282914804172129283014814173130283114824174131283214834175132283314844176133283414854177134283514864178135283614874179136283714884180137283814894181138283914904182139284014914183140284114924184141284214934185142284314944186143284414954187144NONE1496418814528451497418914628461498419014728471499419114828481500419214928491501419315028501502419415128511503419515228521504419615328531505419715428541506419815528551507419915628561508420015728571509420115828581510420215928591511420316028601512420416128611513420516228621514420616328631515420716428641516420816528651517420916628661518421016728671519421116828681520421216928691521421317028701522421417128711523421517228721524421617328731525421717428741526421817528751527421917628761528422017728771529422117828781530422217928791531422318028801532422418128811533422518228821534422618328831535422718428841536422818528851537422918628861538423018728871539423118828881540423218928891541423319028901542423419128911543423519228921544423619328931545423719428941546423819528951547423919628961548424019728971549424119828981550424219928991551424320029001552424420129011553424520229021554424620329031555424720429041556424820529051557424920629061558NONE207290715594250208290815604251209290915614252210291015624253211291115634254212291215644255213291315654256214291415664257215291515674258216291615684259217291715694260218291815704261219291915714262220292015724263221292115734264222292215744265223292315754266224292415764267225292515774268226292615784269227292715794270228292815804271229292915814272230293015824273231293115834274232293215844275233293315854276234293415864277235293515874278236293615884279237293715894280238293815904281239293915914282240294015924283241294115934284242294215944285243294315954286244294415964287245294515974288246294615984289247294715994290248294816004291249294916014292250295016024293251295116034294252295216044295253295316054296254295416064297255295516074298256295616084299257295716094300258295816104301259295916114302260296016124303261296116134304262296216144305263296316154306264296416164307265296516174308266296616184309267296716194310268296816204311269296916214312270297016224313271297116234314272297216244315273297316254316274297416264317275297516274318276297616284319277297716294320278297816304321279297916314322280298016324323281298116334324282298216344325283298316354326284298416364327285298516374328286298616384329287298716394330288298816404331289298916414332290299016424333291299116434334292299216444335293299316454336294299416464337295299516474338296299616484339297299716494340298299816504341299299916514342300300016524343301300116534344302300216544345303300316554346304NONE1656434730530041657434830630051658434930730061659435030830071660435130930081661435231030091662435331130101663NONE312301116644354313301216654355314301316664356315301416674357316301516684358317301616694359318301716704360319301816714361320301916724362321302016734363322302116744364323302216754365324302316764366325302416774367326302516784368327302616794369328302716804370329302816814371330302916824372331303016834373332303116844374333303216854375334303316864376335303416874377336303516884378337303616894379338303716904380339303816914381340303916924382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15348132040142672534913214015267353501322401626745351132340172675535213244018267653531325401926775354132640202678535513274021267953561328402226805357132940232681NONE1330NONE2682535813314024268353591332402526845360133340262685536113344027268653621335402826875363133640292688536413374030268953651338403126905366133940322691536713404033269253681341403426935369134240352694537013434036269553711344403726965372134540382697537313464039269853741347404026995375134840412700537613494042270153771350404327025378135140442703537913524045 TABLE 3COLD RESPONSIVE SEQUENCESSEQAFFYMETRIXID NO:ID NO:111991_G_AT211992_AT311997_AT411998_AT512001_AT612006_S_AT712007_AT812009_AT912018_AT1012022_AT1112026_AT1212031_AT1312047_AT1412051_AT1512052_AT1612053_AT1712060_AT1812072_AT1912074_AT2012102_AT2112112_AT2212117_AT2312125_AT2412130_AT2512143_AT2612145_S_AT2712149_AT2812156_AT2912163_AT3012166_I_AT3112167_AT3212169_I_AT3312175_AT3412176_AT3512179_AT3612187_AT15920_I_AT3712195_AT3812196_AT3912198_AT4012200_AT4112202_AT4212214_G_AT4312219_AT4412224_AT4512226_AT4612233_AT4712240_AT4812253_G_AT4912256_AT5012269_S_AT5112270_AT5212284_AT5312287_S_AT17570_G_AT5412293_AT5512294_S_AT5612300_AT5712307_AT5812312_AT5912315_AT6012324_I_AT6112331_S_AT6212336_AT6312344_AT6412348_AT6512353_AT6612359_S_AT6712372_AT6812374_I_AT12726_F_AT6912390_AT7012395_S_AT7112405_AT7212408_AT7312410_G_AT7412419_AT7512427_AT7612431_AT7712436_AT7812438_AT7912443_S_AT8012447_AT8112450_S_AT8212452_AT8312474_AT8412477_AT8512491_AT8612497_AT8712500_S_AT8812503_AT8912515_AT9012516_S_AT9112523_AT9212526_AT9312527_AT9412532_AT9512534_G_AT9612544_AT9712549_S_AT9812550_S_AT17103_S_AT9912552_AT10012555_S_AT10112576_S_AT10212581_S_AT16645_S_AT10312587_AT10412597_AT10512602_AT10612610_AT10712631_AT10812646_AT10912649_AT11012650_AT11112653_AT11212661_AT11312666_AT11412674_AT11512675_S_AT11612678_I_AT11712681_S_AT11812688_AT11912702_AT12012705_F_AT12112736_F_AT12212737_F_AT12312758_AT12412760_G_AT12512762_R_AT12612764_F_AT12712766_AT15115_F_AT12812767_AT12912768_AT13012772_AT13112773_AT13212776_AT13312788_AT13412793_AT13512794_AT13612802_AT13712809_G_AT13812812_AT13912815_AT14012816_AT14112818_AT14212824_S_AT14312828_S_AT14412842_S_AT14512846_S_AT14612858_AT14712860_S_AT14812861_S_AT14912881_S_AT17600_S_AT15012889_S_AT15112901_S_AT15212902_AT15312904_S_AT15412905_S_AT15512908_S_AT15612910_S_AT16385_S_AT15712914_S_AT15783_S_AT17645_S_AT15812916_S_AT15912923_S_AT16012926_S_AT16112927_S_AT16212931_S_AT16312937_R_AT16412941_G_AT16512942_AT16612947_AT16712949_AT16812953_AT16912956_I_AT17012959_AT17112966_S_AT17212975_AT17312983_AT17412984_AT17512987_S_AT17612994_S_AT17713002_AT17813009_I_AT17913011_AT18013018_AT18113023_AT18213024_AT18313034_S_AT18413046_G_AT18513048_S_AT13495_S_AT18613054_AT18713067_S_AT18813068_AT18913073_S_AT19013078_S_AT19113079_AT19213081_S_AT19313083_AT19413086_R_AT19513087_AT19613090_AT19713092_S_AT16950_S_AT19813098_AT19913100_AT20013103_AT20113105_AT20213107_S_AT20313108_AT20413109_AT20513114_AT20613118_F_AT20713119_AT20813120_AT20913123_AT21013128_AT21113133_S_AT17430_S_AT21213135_S_AT21313139_AT21413140_AT21513143_AT21613151_G_AT21713160_AT21813161_AT21913162_AT22013165_AT22113166_AT22213167_AT22313179_AT22413181_AT22513185_AT22613193_S_AT22713213_S_AT16004_S_AT22813219_S_AT20288_G_AT22913220_S_AT13221_AT18929_S_AT23013233_AT14301_S_AT23113243_R_AT23213254_S_AT23313260_S_AT15660_S_AT23413273_S_AT16105_S_AT23513274_S_AT17077_S_AT23613276_S_AT23713278_F_AT23813285_S_AT23913288_S_AT17043_S_AT24013292_S_AT24113296_S_AT24213297_S_AT24313299_S_AT15166_S_AT24413332_AT24513347_AT24613351_AT24713352_AT24813355_AT24913404_AT25013422_AT25113459_AT25213460_AT25313461_S_AT25413467_AT25513488_AT25613523_S_AT25713529_AT25813539_I_AT14631_S_AT25913541_AT26013542_AT26113545_S_AT26213552_AT26313556_I_AT26413561_AT26513563_S_AT26613567_AT26713568_AT26813571_AT26913575_AT27013576_AT27113583_AT27213598_AT27313601_AT27413604_AT27513613_AT27613616_S_AT16544_S_AT27713617_AT27813618_S_AT27913619_AT28013621_G_AT28113623_R_AT28213629_S_AT28313631_AT28413635_AT28513646_AT28613650_AT28713653_AT28813655_AT28913656_AT29013657_AT29113666_S_AT17083_S_AT29213667_S_AT29313669_S_AT17074_S_AT29413670_S_AT15206_S_AT29513671_S_AT16805_S_AT29613678_S_AT29713688_S_AT29813690_S_AT16065_S_AT29913691_S_AT16117_S_AT30013692_S_AT16118_S_AT30113700_AT30213704_S_AT30313714_AT30413715_AT30513724_AT30613748_AT30713759_AT30813767_AT30913785_AT31013803_AT31113850_I_AT31213876_AT31313880_S_AT31413883_AT31513887_S_AT31613895_AT31713904_S_AT18722_S_AT31813906_S_AT31913908_S_AT18597_AT32013923_AT32113927_AT32213932_AT32313935_AT32413940_AT32513949_S_AT32613954_G_AT32713971_S_AT32813973_AT32913983_AT33013985_S_AT33113987_S_AT18738_F_AT33213989_AT20674_S_AT33314010_AT33414013_AT33514014_AT33614019_AT33714021_R_AT33814025_S_AT18909_S_AT33914027_AT34014030_AT34114044_AT34214048_AT34314056_AT34414057_AT34514058_AT34614059_AT34714061_AT34814068_S_AT34914072_AT35014073_AT35114074_AT35214084_AT35314095_S_AT35414100_AT35514101_AT35614103_AT35714105_AT35814106_AT35914121_AT36014129_S_AT36114133_S_AT36214143_AT36314145_AT36414148_AT36514186_AT36614194_AT36714196_AT36814223_AT36914234_AT37014236_AT37114251_F_AT37214252_F_AT37314270_AT37414298_G_AT17581_G_AT37514303_S_AT37614312_AT37714316_AT37814339_AT37914366_AT38014369_AT38114388_AT38214392_G_AT38314393_AT38414421_AT38514436_AT38614448_AT38714450_AT38814454_AT38914459_AT39014478_AT39114482_AT39214485_AT39314492_S_AT39414505_AT39514510_AT39614511_AT39714517_AT39814519_AT39914525_S_AT40014527_AT40114534_S_AT40214538_R_AT40314554_AT40414558_AT40514559_S_AT40614566_AT40714572_AT40814579_AT40914587_AT41014591_AT41114595_AT41214602_AT41314603_AT41414605_AT41514620_S_AT41614626_S_AT41714630_S_AT16559_S_AT41814637_S_AT17122_S_AT41914642_F_AT42014650_S_AT15150_S_AT42114654_S_AT42214667_S_AT18299_S_AT42314669_S_AT16136_S_AT42414672_S_AT42514679_S_AT42614682_I_AT42714689_AT42814697_G_AT16902_AT42914701_S_AT14734_S_AT43014703_AT43114711_S_AT43214712_S_AT20530_S_AT43314713_S_AT43414715_S_AT43514728_S_AT43614731_S_AT43714781_AT43814797_S_AT43914800_AT44014809_AT44114843_AT44214847_AT44314872_AT44414886_AT44514896_AT44614900_AT44714908_AT44814912_AT44914914_AT45014942_AT45114945_AT45214955_AT45314957_S_AT45414958_AT45514965_AT45614974_AT45714980_AT45814981_AT45914984_S_AT46014995_AT46115004_AT46215009_AT46315010_AT46415024_AT46515026_AT46615036_R_AT46715054_AT46815056_AT46915057_AT47015066_AT47115073_AT47215081_AT47315083_AT47415091_AT47515097_S_AT47615101_S_AT47715102_S_AT47815107_S_AT47915112_S_AT48015116_F_AT48115118_S_AT48215122_S_AT48315130_S_AT48415131_S_AT48515132_S_AT17585_S_AT48615139_S_AT48715143_S_AT48815146_S_AT48915159_S_AT15160_S_AT49015162_S_AT49115167_S_AT49215171_S_AT49315174_F_AT49415178_S_AT49515185_S_AT18023_S_AT49615188_S_AT49715193_S_AT49815196_S_AT49915197_S_AT50015201_F_AT50115213_S_AT50215243_AT50315256_AT50415270_AT50515319_AT50615325_AT50715337_AT50815341_AT50915343_AT51015348_AT51115350_AT51215355_S_AT51315367_AT51415372_AT51515379_AT51615381_AT51715383_AT51815384_AT51915385_AT52015387_AT52115410_AT52215417_S_AT52315422_AT52415423_AT52515431_AT52615433_AT52715452_AT52815464_AT52915468_AT53015471_AT53115472_AT53215475_S_AT53315485_AT53415489_AT53515490_AT53615503_AT53715505_AT53815510_R_AT53915512_AT54015514_AT54115515_R_AT54215517_S_AT54315518_AT54415529_AT54515534_F_AT54615538_AT54715541_AT54815543_AT54915544_AT55015551_AT55115574_S_AT55215576_S_AT55315577_S_AT55415578_S_AT55515583_S_AT55615588_S_AT55715595_S_AT55815600_S_AT55915602_F_AT56015608_S_AT56115613_S_AT56215616_S_AT56315618_S_AT56415620_S_AT56515627_S_AT56615634_S_AT16125_S_AT18046_S_AT56715637_S_AT56815639_S_AT56915642_S_AT57015643_S_AT57115651_F_AT57215652_S_AT57315665_S_AT57415667_S_AT18610_S_AT57515668_S_AT57615671_S_AT57715675_S_AT57815679_S_AT57915685_S_AT58015687_F_AT58115688_S_AT58215689_S_AT58315692_S_AT58415694_S_AT58515712_S_AT58615808_AT58715845_AT58815848_AT58915850_AT20406_G_AT59015858_AT59115862_AT59215868_AT59315878_AT59415894_AT59515900_AT59615901_AT59715902_AT59815912_AT59915913_AT60015928_AT60115940_AT60215941_AT60315945_AT60415948_S_AT60515956_AT60615960_AT16466_S_AT60715976_AT60815978_AT60915986_S_AT61015990_AT61116009_S_AT61216015_AT61316019_AT61416024_AT61516034_AT61616036_I_AT18729_AT61716039_S_AT61816040_AT61916042_S_AT62016047_AT62116049_S_AT62216051_S_AT62316055_S_AT62416059_S_AT62516062_S_AT62616066_S_AT62716069_S_AT62816074_S_AT62916076_S_AT63016077_S_AT17579_S_AT63116079_S_AT63216084_S_AT17998_S_AT63316087_S_AT63416089_S_AT63516090_S_AT63616102_S_AT63716103_S_AT63816108_S_AT63916112_S_AT64016134_S_AT64116137_S_AT64216138_S_AT64316140_S_AT64416143_S_AT64516145_S_AT64616148_S_AT64716151_S_AT64816155_S_AT64916158_F_AT65016160_F_AT65116162_S_AT65216168_S_AT65316169_S_AT65416171_S_AT65516172_S_AT65616184_AT65716192_AT65816222_AT65916242_AT66016244_AT66116250_AT66216286_AT66316288_AT66416294_S_AT66516296_AT66616297_AT66716325_AT66816346_S_AT66916357_AT67016380_AT67116382_AT67216393_S_AT67316402_S_AT67416411_S_AT67516442_S_AT67616446_AT67716448_G_AT67816453_S_AT67916457_S_AT68016465_AT16916_S_AT68116470_S_AT18735_S_AT68216481_S_AT68316486_AT68416487_AT68516488_AT68616496_S_AT68716499_AT68816510_AT68916511_AT69016512_S_AT18085_R_AT69116514_AT69216516_AT69316517_AT69416526_AT69516528_AT69616531_S_AT69716535_S_AT69816537_S_AT69916538_S_AT70016543_S_AT70116550_S_AT70216554_S_AT70316567_S_AT70416571_S_AT70516576_F_AT70616577_S_AT70716579_S_AT70816580_S_AT70916583_S_AT71016584_S_AT18706_S_AT71116593_S_AT71216595_S_AT71316598_S_AT71416604_S_AT71516605_S_AT71616610_S_AT71716611_S_AT71816614_S_AT71916617_S_AT72016618_S_AT72116620_S_AT72216621_S_AT72316631_S_AT72416634_S_AT72516635_S_AT72616636_S_AT72716639_S_AT72816640_S_AT72916650_S_AT73016652_S_AT73116654_AT73216672_AT73316673_AT73416687_S_AT73516747_AT73616753_AT73716768_AT73816777_AT73916784_AT74016807_AT74116811_AT74216845_AT74316894_AT74416899_AT74516911_AT74616920_AT74716921_AT74816924_S_AT74916926_S_AT75016931_S_AT75116934_S_AT75216937_AT75316938_AT75416942_AT75516943_S_AT18231_AT75616949_S_AT75716952_S_AT75816956_AT75916962_S_AT76016965_S_AT76116970_S_AT18010_S_AT76216977_AT76316984_AT76416996_S_AT76516997_AT76617000_AT76717005_AT76817010_S_AT76917017_S_AT77017031_S_AT77117033_S_AT77217053_S_AT77317055_S_AT77417063_S_AT77517068_S_AT77617070_S_AT77717075_S_AT77817084_S_AT77917087_S_AT78017092_S_AT78117095_S_AT78217096_S_AT78317102_S_AT78417105_S_AT78517109_S_AT78617110_S_AT78717113_S_AT78817115_S_AT78917116_S_AT79017123_S_AT79117129_S_AT79217132_AT79317166_AT79417206_AT79517207_AT79617215_AT79717237_AT79817247_AT79917254_AT80017286_AT80117288_S_AT80217292_AT80317300_AT80417303_S_AT80517318_AT80617319_AT80717322_AT80817323_AT80917332_S_AT81017374_AT81117381_AT81217388_AT81317392_S_AT81417405_AT81517415_AT81617418_S_AT81717420_AT81817423_S_AT81917426_AT82017427_AT82117429_S_AT82217431_AT82317439_G_AT82417457_AT82517458_AT82617462_S_AT82717463_AT82817465_AT82917466_S_AT83017475_AT83117479_AT83217482_S_AT83317495_S_AT83417508_S_AT83517522_S_AT83617523_S_AT83717537_S_AT83817538_S_AT83917539_S_AT84017546_S_AT18694_S_AT84117557_S_AT84217560_S_AT84317562_AT84417564_S_AT19361_S_AT84517565_S_AT84617568_AT84717573_AT84817577_G_AT84917578_AT85017596_AT85117627_AT85217631_AT85317632_AT85417672_AT85517675_AT85617677_AT85717732_AT85817743_AT85917748_AT86017782_AT86117823_S_AT86217841_AT86317849_S_AT86417852_G_AT86517857_AT86617865_AT86717882_AT86817885_AT86917900_S_AT87017910_AT87117911_AT87217916_AT87317917_S_AT87417918_AT87517921_S_AT87617922_AT87717926_S_AT87817933_AT87917935_AT88017956_I_AT88117966_AT88217967_AT88317970_I_AT88417978_S_AT20635_S_AT88517986_S_AT88617993_AT88718001_AT88818003_AT88918004_AT89018005_AT89118029_G_AT18030_I_AT89218040_S_AT89318045_AT89418064_R_AT89518065_R_AT89618074_AT89718076_S_AT89818077_AT89918081_AT90018154_S_AT18365_S_AT90118165_AT90218174_AT90318176_AT90418194_I_AT90518197_AT90618198_AT90718213_AT90818219_AT90918221_AT91018222_AT91118226_S_AT91218232_AT91318237_AT91418241_AT91518257_AT91618258_S_AT91718269_S_AT91818274_S_AT91918275_AT92018278_AT92118282_AT92218283_AT92318290_AT92418291_AT92518306_AT92618316_AT92718317_AT92818327_S_AT92918337_S_AT93018339_AT93118347_S_AT93218383_AT93318390_AT93418439_S_AT93518465_S_AT93618487_AT93718508_S_AT93818512_AT93918543_AT94018544_AT94118552_AT94218555_AT94318556_AT94418561_AT94518567_AT94618573_AT94718580_AT94818581_AT94918584_AT95018587_S_AT95118588_AT95218591_AT95318592_S_AT95418600_AT95518601_S_AT95618607_S_AT95718611_AT95818616_AT95918622_G_AT96018623_AT96118628_AT96218631_AT96318635_AT96418636_AT96518638_AT96618652_AT96718657_AT96818659_AT96918660_S_AT97018667_AT97118675_AT97218684_AT97318686_S_AT97418688_S_AT97518693_S_AT97618698_S_AT97718705_AT97818707_AT97918708_AT98018726_S_AT98118727_AT98218732_I_AT98318736_AT98418750_F_AT98518754_AT98618778_AT98718806_S_AT98818823_S_AT98918829_AT99018835_AT99118844_AT99218859_AT99318864_AT99418866_AT99518880_AT99618883_G_AT99718885_AT99818886_AT99918887_AT100018888_AT100118889_AT100218892_S_AT100318901_AT100418911_AT100518917_I_AT100618939_AT100718947_I_AT100818950_AT100918951_S_AT101018954_AT101118956_AT101218959_AT101318966_AT101418974_AT101518976_AT101618980_AT101718989_S_AT101818994_AT101919030_AT102019039_AT102119049_AT102219083_AT102319115_AT102419117_S_AT102519122_AT102619125_S_AT102719127_AT102819130_AT102919144_AT103019157_S_AT103119178_AT103219190_G_AT103319198_AT103419202_AT103519209_S_AT103619211_AT103719218_AT103819222_AT103919226_G_AT104019229_AT104119230_AT104219232_S_AT104319285_AT104419326_AT104519332_AT104619346_AT104719347_AT104819362_AT104919363_AT105019364_AT105119367_AT105219373_AT105319381_AT105419382_AT105519384_AT105619401_AT105719406_AT105819413_AT105919416_AT106019426_S_AT106119439_AT106219441_S_AT106319442_AT106419448_S_AT106519454_AT106619462_S_AT106719464_AT106819470_AT106919483_AT107019489_S_AT107119513_AT107219548_AT107319562_AT107419563_S_AT107519567_AT107619581_AT107719589_S_AT107819595_S_AT107919606_AT108019623_AT108119624_AT108219627_S_AT108319636_AT108419652_AT108519655_AT108619657_S_AT108719658_AT108819660_AT108919665_S_AT109019667_AT109119671_AT109219677_AT109319686_AT109419689_AT109519690_S_AT109619695_AT109719698_AT109819700_S_AT109919708_AT110019717_AT110119726_S_AT110219744_AT110319752_S_AT110419759_AT110519782_AT110619803_S_AT110719828_AT110819831_I_AT110919833_S_AT111019834_AT111119836_AT111219841_AT111319845_G_AT111419854_AT111519855_AT111619866_AT111719867_AT111819870_S_AT111919871_AT112019872_AT112119875_S_AT112219876_AT112319879_S_AT112419881_AT112519897_S_AT112619903_AT112719905_AT112819906_AT112919907_AT113019910_AT113119913_AT113219920_S_AT113319932_AT113419939_AT113519945_AT113619947_AT113719951_AT113819956_AT113919962_AT114019963_AT114119969_AT114219970_S_AT114319971_AT114419972_AT114519981_AT114619990_AT114719996_AT114820003_S_AT114920009_S_AT115020013_AT115120018_AT115220024_S_AT115320027_AT115420045_AT115520047_AT115620048_AT115720050_AT115820051_AT115920058_AT116020067_AT116120068_AT116220069_AT116320093_I_AT116420099_AT116520100_AT116620113_S_AT116720117_AT116820123_AT116920127_S_AT117020129_AT117120150_AT117220154_AT117320156_AT117420165_AT117520173_AT117620178_S_AT117720183_AT117820188_AT117920189_AT118020197_AT118120210_G_AT118220213_AT118320229_AT118420232_S_AT118520255_AT118620257_AT118720262_AT118820275_AT118920278_S_AT119020282_S_AT119120284_AT119220293_AT119320294_AT119420312_S_AT119520315_I_AT119620330_S_AT119720331_AT119820350_S_AT119920354_S_AT120020355_AT120120360_AT120220363_AT120320369_S_AT120420378_G_AT120520383_AT120620384_AT120720387_AT120820393_AT120920396_AT121020399_AT121120409_G_AT121220412_S_AT121320413_AT121420439_AT121520440_AT121620444_AT121720445_AT121820449_AT121920456_AT122020462_AT122120471_AT122220474_AT122320495_S_AT122420499_AT122520501_AT122620511_AT122720515_S_AT122820516_AT122920517_AT123020518_AT123120520_S_AT123220536_S_AT123320538_S_AT123420539_S_AT123520558_AT123620561_AT123720567_AT123820571_AT123920582_S_AT124020586_I_AT124120590_AT124220592_AT124320594_AT124420608_S_AT124520612_S_AT124620616_AT124720620_G_AT124820637_AT124920643_AT125020649_AT125120651_AT125220654_S_AT125320670_AT125420684_AT125520685_AT125620693_AT125720701_S_AT125820704_AT125920705_AT126020715_AT126120719_AT TABLE 42X UP IN COLD, ONLY11997_at12688_at13274_s_at14145_at15083_at15639_s_at11998_at12701_i_at13278_f_at14170_at15084_at15641_s_at12018_at12702_at13279_s_at14186_at15096_at15660_s_at12031_at12719_f_at13285_s_at14196_at15101_s_at15665_s_at12047_at12726_f_at13288_s_at14227_at15105_s_at15687_f_at12051_at12736_f_at13292_s_at14234_at15112_s_at15694_s_at12053_at12754_g_at13297_s_at14250_r_at15115_f_at15712_s_at12060_at12762_r_at13299_s_at14270_at15116_f_at15783_s_at12072_at12766_at13332_at14298_g_at15122_s_at15808_at12074_at12767_at13351_at14303_s_at15126_s_at15837_at12102_at12768_at13352_at14312_at15131_s_at15850_at12112_at12773_at13422_at14339_at15132_s_at15862_at12117_at12788_at13435_at14388_at15137_s_at15868_at12130_at12802_at13461_s_at14393_at15144_s_at15878_at12145_s_at12860_s_at13467_at14511_at15148_s_at15901_at12151_at12861_s_at13488_at14525_s_at15153_s_at15912_at12163_at12879_s_at13495_s_at14527_at15159_s_at15920_i_at12175_at12891_at13539_i_at14534_s_at15160_s_at15941_at12187_at12914_s_at13542_at14554_at15166_s_at15945_at12195_at12927_s_at13575_at14566_at15174_f_at15960_at12219_at12947_at13577_s_at14579_at15197_s_at15990_at12256_at12956_i_at13617_at14591_at15270_at16001_at12269_s_at12966_s_at13634_s_at14595_at15319_at16009_s_at12307_at12974_at13656_at14600_at15325_at16010_s_at12315_at12987_s_at13671_s_at14631_s_at15337_at16034_at12336_at12994_s_at13691_s_at14635_s_at15341_at16036_i_at12349_s_at12998_at13700_at14679_s_at15343_at16039_s_at12353_at13002_at13704_s_at14691_at15355_s_at16040_at12359_s_at13018_at13709_s_at14697_g_at15367_at16042_s_at12390_at13023_at13715_at14709_at15379_at16047_at12395_s_at13046_g_at13785_at14711_s_at15381_at16049_s_at12431_at13054_at13803_at14728_s_at15410_at16051_s_at12436_at13086_r_at13812_s_at14731_s_at15417_s_at16062_s_at12443_s_at13087_at13825_s_at14797_s_at15422_at16079_s_at12447_at13100_at13850_i_at14809_at15433_at16087_s_at12452_at13109_at13904_s_at14843_at15451_at16090_s_at12477_at13119_at13908_s_at14847_at15452_at16117_s_at12503_at13120_at13927_at14872_at15453_s_at16118_s_at12516_s_at13128_at13971_s_at14886_at15472_at16137_s_at12532_at13134_s_at13985_s_at14896_at15489_at16155_s_at12544_at13140_at14013_at14897_at15490_at16162_s_at12561_at13143_at14019_at14900_at15503_at16184_at12602_at13167_at14021_r_at14956_s_at15510_r_at16192_at12610_at13172_s_at14028_at14958_at15517_s_at16222_at12631_at13178_at14048_at14965_at15518_at16244_at12647_s_at13179_at14058_at14984_s_at15544_at16250_at12650_at13181_at14059_at15004_at15588_s_at16260_at12656_at13187_i_at14064_at15010_at15600_s_at16286_at12674_at13209_s_at14073_at15036_r_at15605_s_at16296_at12675_s_at13219_s_at14105_at15040_g_at15613_s_at16297_at12676_s_at13221_at14106_at15046_s_at15614_s_at16342_at12681_s_at13243_r_at14126_s_at15057_at15616_s_at16367_i_at12686_s_at13260_s_at14140_at15073_at15633_s_at16411_s_at16442_s_at17077_s_at17978_s_at18885_at19689_at20412_s_at16465_at17102_s_at17999_at18887_at19698_at20413_at16466_s_at17109_s_at18001_at18888_at19700_s_at20432_at16468_at17113_s_at18004_at18889_at19707_s_at20433_at16486_at17123_s_at18012_s_at18901_at19708_at20456_at16487_at17128_s_at18040_s_at18907_s_at19713_at20462_at16488_at17129_s_at18176_at18917_i_at19718_at20471_at16489_at17132_at18194_i_at18939_at19744_at20511_at16496_s_at17166_at18197_at18947_i_at19836_at20515_s_at16499_at17206_at18198_at18949_at19839_at20517_at16511_at17237_at18213_at18954_at19840_s_at20518_at16517_at17300_at18219_at18959_at19845_g_at20529_at16538_s_at17319_at18222_at18974_at19854_at20536_s_at16554_s_at17322_at18231_at18976_at19855_at20538_s_at16571_s_at17332_s_at18232_at18980_at19860_at20539_s_at16576_f_at17381_at18241_at18989_s_at19866_at20576_at16595_s_at17388_at18269_s_at19019_i_at19871_at20582_s_at16605_s_at17392_s_at18272_at19049_at19875_s_at20586_i_at16610_s_at17408_at18282_at19083_at19879_s_at20608_s_at16620_s_at17424_at18298_at19130_at19881_at20649_at16621_s_at17429_s_at18316_at19156_s_at19913_at20651_at16635_s_at17457_at18317_at19178_at19939_at20684_at16636_s_at17458_at18331_s_at19190_g_at19945_at20685_at16638_s_at17466_s_at18347_s_at19199_at19947_at20699_at16650_s_at17477_s_at18383_at19202_at19951_at20705_at16672_at17482_s_at18390_at19209_s_at19956_at20715_at16673_at17538_s_at18455_at19211_at19971_at16687_s_at17546_s_at18465_s_at19218_at19976_at16747_at17562_at18544_at19229_at19998_at16753_at17581_g_at18555_at19322_at20003_s_at16768_at17627_at18556_at19326_at20015_at16805_s_at17631_at18560_at19359_s_at20027_at16807_at17632_at18561_at19367_at20051_at16845_at17645_s_at18571_at19384_at20068_at16847_at17672_at18588_at19389_at20093_i_at16896_s_at17675_at18597_at19397_at20117_at16899_at17677_at18601_s_at19406_at20150_at16902_at17693_at18611_at19426_s_at20156_at16911_at17732_at18623_at19441_s_at20165_at16914_s_at17743_at18635_at19442_at20257_at16943_s_at17748_at18659_at19470_at20262_at16956_at17775_at18660_s_at19489_s_at20275_at16996_s_at17782_at18673_at19562_at20282_s_at17010_s_at17841_at18694_s_at19577_at20288_g_at17016_s_at17852_g_at18705_at19589_s_at20293_at17032_s_at17900_s_at18708_at19597_s_at20315_i_at17033_s_at17901_at18738_f_at19611_s_at20330_s_at17043_s_at17911_at18750_f_at19624_at20360_at17050_s_at17921_s_at18778_at19657_s_at20363_at17055_s_at17922_at18829_at19667_at20369_s_at17068_s_at17933_at18835_at19671_at20384_at17071_s_at17967_at18866_at19677_at20393_at17075_s_at17970_i_at18875_s_at19686_at20396_at TABLE 52X UP COLD 3 HR, ONLY12117_at12145_s_at12151_at12163_at12187_at12256_at12315_at12349_s_at12353_at12359_s_at12544_at12602_at12610_at12676_s_at12686_s_at12701_i_at12702_at12719_f_at12736_f_at12754_g_at12766_at12767_at12768_at12773_at12788_at12879_s_at12891_at12947_at12966_s_at12974_at12994_s_at13002_at13100_at13140_at13167_at13172_s_at13179_at13187_i_at13219_s_at13260_s_at13278_f_at13279_s_at13285_s_at13288_s_at13292_s_at13297_s_at13351_at13352_at13435_at13467_at13488_at13495_s_at13656_at13671_s_at13691_s_at13785_at13803_at13825_s_at13904_s_at14013_at14021_r_at14028_at14064_at14126_s_at14145_at14170_at14196_at14250_r_at14298_g_at14303_s_at14339_at14527_at14534_s_at14554_at14595_at14635_s_at14679_s_at14691_at14697_g_at14709_at14728_s_at14809_at14896_at14965_at14984_s_at15046_s_at15083_at15096_at15105_s_at15115_f_at15116_f_at15122_s_at15126_s_at15131_s_at15132_s_at15137_s_at15153_s_at15159_s_at15160_s_at15197_s_at15355_s_at15379_at15417_s_at15422_at15451_at15452_at15453_s_at15489_at15518_at15588_s_at15613_s_at15614_s_at15616_s_at15639_s_at15641_s_at15660_s_at15687_f_at15694_s_at15862_at15868_at15878_at15901_at16034_at16039_s_at16040_at16042_s_at16047_at16062_s_at16087_s_at16117_s_at16118_s_at16162_s_at16184_at16222_at16250_at16411_s_at16442_s_at16465_at16486_at16488_at16489_at16517_at16571_s_at16605_s_at16610_s_at16620_s_at16636_s_at16650_s_at16805_s_at16845_at16899_at16914_s_at16943_s_at16996_s_at17010_s_at17043_s_at17068_s_at17109_s_at17128_s_at17237_at17319_at17392_s_at17429_s_at17477_s_at17538_s_at17581_g_at17627_at17672_at17693_at17782_at17841_at17900_s_at17933_at17978_s_at18001_at18012_s_at18198_at18219_at18241_at18269_s_at18272_at18282_at18298_at18383_at18556_at18588_at18601_s_at18611_at18694_s_at18708_at18738_f_at18778_at18829_at18835_at18866_at18875_s_at18888_at18907_s_at18917_i_at18939_at18974_at19190_g_at19199_at19202_at19211_at19384_at19406_at19426_s_at19442_at19470_at19577_at19597_s_at19624_at19657_s_at19667_at19845_g_at19855_at19866_at19945_at19951_at19998_at20003_s_at20015_at20051_at20093_i_at20117_at20288_g_at20360_at20369_s_at20384_at20462_at20471_at20515_s_at20538_s_at20576_at20608_s_at20651_at20685_at20705_at TABLE 62X DOWN COLD, ONLY11991_g_at12450_s_at12881_s_at13151_g_at13621_g_at14056_at11992_at12474_at12889_s_at13160_at13623_r_at14057_at12001_at12491_at12901_s_at13161_at13629_s_at14061_at12006_s_at12497_at12902_at13162_at13631_at14067_at12007_at12500_s_at12904_s_at13165_at13635_at14068_s_at12009_at12515_at12905_s_at13166_at13646_at14072_at12022_at12521_at12908_s_at13185_at13650_at14074_at12023_s_at12523_at12910_s_at13193_s_at13652_at14075_at12026_at12526_at12916_s_at13211_s_at13653_at14083_at12037_at12527_at12923_s_at13213_s_at13655_at14084_at12052_at12534_g_at12926_s_at13219_s_at13657_at14089_at12125_at12549_s_at12931_s_at13233_at13666_s_at14095_s_at12143_at12550_s_at12937_r_at13236_s_at13667_s_at14096_at12149_at12552_at12941_g_at13239_s_at13669_s_at14100_at12156_at12555_s_at12942_at13241_s_at13670_s_at14101_at12166_i_at12556_at12949_at13254_s_at13672_s_at14103_at12167_at12575_s_at12953_at13266_s_at13678_s_at14121_at12169_i_at12576_s_at12958_at13273_s_at13679_s_at14129_s_at12176_at12581_s_at12959_at13275_f_at13688_s_at14133_s_at12179_at12587_at12966_s_at13276_s_at13690_s_at14143_at12196_at12597_at12975_at13278_f_at13691_s_at14148_at12198_at12606_at12983_at13280_s_at13692_s_at14162_at12200_at12609_at12984_at13285_s_at13714_at14194_at12202_at12646_at13002_at13296_s_at13724_at14208_at12212_at12649_at13009_i_at13347_at13748_at14217_at12214_g_at12653_at13011_at13355_at13751_at14223_at12224_at12661_at13014_at13361_at13759_at14235_at12226_at12666_at13024_at13404_at13767_at14236_at12233_at12678_i_at13034_s_at13406_at13789_at14251_f_at12240_at12705_f_at13041_s_at13459_at13876_at14252_f_at12253_g_at12736_f_at13048_s_at13460_at13880_s_at14285_at12270_at12737_f_at13067_s_at13464_at13883_at14301_s_at12278_at12758_at13068_at13523_s_at13887_s_at14316_at12284_at12760_g_at13073_s_at13529_at13895_at14366_at12287_s_at12764_f_at13078_s_at13541_at13906_s_at14369_at12293_at12765_at13079_at13545_s_at13919_at14392_g_at12294_s_at12772_at13081_s_at13550_at13923_at14421_at12300_at12776_at13083_at13552_at13932_at14431_at12312_at12784_at13090_at13556_i_at13935_at14436_at12315_at12793_at13092_s_at13561_at13940_at14448_at12324_i_at12794_at13098_at13563_s_at13949_s_at14450_at12331_s_at12795_at13103_at13567_at13954_g_at14454_at12344_at12809_g_at13105_at13568_at13973_at14459_at12348_at12812_at13107_s_at13571_at13983_at14478_at12353_at12815_at13108_at13576_at13989_at14482_at12372_at12816_at13114_at13583_at14010_at14485_at12374_i_at12818_at13118_f_at13598_at14014_at14492_s_at12405_at12824_s_at13123_at13601_at14015_s_at14505_at12408_at12828_s_at13124_at13604_at14016_s_at14510_at12410_g_at12842_s_at13133_s_at13613_at14025_s_at14517_at12419_at12846_s_at13135_s_at13616_s_at14027_at14519_at12427_at12858_at13139_at13618_s_at14030_at14534_s_at19438_at12869_s_at13146_s_at13619_at14044_at14538_r_at14558_at15047_at15512_at15940_at16357_at16894_at14559_s_at15054_at15514_at15948_s_at16380_at16899_at14572_at15056_at15515_r_at15956_at16382_at16920_at14584_at15058_s_at15529_at15976_at16385_s_at16921_at14587_at15063_at15534_f_at15978_at16393_s_at16924_s_at14595_at15066_at15538_at15986_s_at16402_s_at16926_s_at14602_at15081_at15541_at16004_s_at16417_s_at16931_s_at14603_at15091_at15543_at16015_at16442_s_at16934_s_at14605_at15097_s_at15551_at16017_at16446_at16937_at14620_s_at15102_s_at15574_s_at16019_at16448_g_at16938_at14626_s_at15107_s_at15576_s_at16024_at16453_s_at16942_at14630_s_at15118_s_at15577_s_at16031_at16457_s_at16949_s_at14637_s_at15127_s_at15578_s_at16055_s_at16470_s_at16950_s_at14640_s_at15130_s_at15581_s_at16059_s_at16481_s_at16952_s_at14642_f_at15132_s_at15583_s_at16065_s_at16510_at16962_s_at14650_s_at15133_s_at15591_s_at16066_s_at16512_s_at16965_s_at14654_s_at15139_s_at15595_s_at16069_s_at16514_at16970_s_at14667_s_at15143_s_at15602_f_at16074_s_at16516_at16977_at14668_s_at15146_s_at15606_s_at16076_s_at16523_s_at16984_at14669_s_at15150_s_at15608_s_at16077_s_at16526_at16989_at14672_s_at15161_s_at15616_s_at16084_s_at16528_at16993_at14673_s_at15162_s_at15618_s_at16089_s_at16531_s_at16997_at14675_s_at15167_s_at15620_s_at16102_s_at16535_s_at17000_at14679_s_at15170_s_at15627_s_at16103_s_at16537_s_at17005_at14681_g_at15171_s_at15634_s_at16105_s_at16543_s_at17010_s_at14682_i_at15178_s_at15637_s_at16108_s_at16544_s_at17017_s_at14689_at15182_s_at15642_s_at16112_s_at16550_s_at17031_s_at14701_s_at15185_s_at15643_s_at16117_s_at16559_s_at17040_s_at14703_at15188_s_at15646_s_at16118_s_at16567_s_at17053_s_at14712_s_at15193_s_at15651_f_at16125_s_at16577_s_at17056_s_at14713_s_at15196_s_at15652_s_at16127_s_at16579_s_at17063_s_at14715_s_at15201_f_at15667_s_at16134_s_at16580_s_at17070_s_at14734_s_at15206_s_at15668_s_at16136_s_at16583_s_at17074_s_at14781_at15207_s_at15670_s_at16138_s_at16584_s_at17084_s_at14800_at15213_s_at15671_s_at16140_s_at16593_s_at17085_s_at14856_s_at15243_at15675_s_at16143_s_at16598_s_at17087_s_at14882_at15256_at15679_s_at16144_s_at16603_s_at17092_s_at14908_at15348_at15685_s_at16145_s_at16604_s_at17095_s_at14912_at15350_at15688_s_at16148_s_at16611_s_at17096_s_at14914_at15372_at15689_s_at16151_s_at16614_s_at17097_s_at14924_at15383_at15692_s_at16158_f_at16617_s_at17103_s_at14942_at15384_at15775_at16160_f_at16618_s_at17105_s_at14945_at15385_at15776_at16168_s_at16620_s_at17110_s_at14955_at15387_at15845_at16169_s_at16631_s_at17115_s_at14957_s_at15406_at15848_at16171_s_at16634_s_at17116_s_at14974_at15423_at15858_at16172_s_at16639_s_at17119_s_at14980_at15431_at15866_s_at16222_at16640_s_at17122_s_at14981_at15464_at15894_at16232_s_at16652_s_at17207_at14995_at15468_at15900_at16242_at16654_at17215_at15009_at15471_at15901_at16288_at16777_at17247_at15018_at15475_s_at15902_at16294_s_at16784_at17254_at15024_at15485_at15913_at16325_at16811_at17286_at15026_at15505_at15928_at16346_s_at16893_at17288_s_at17292_at17910_at18337_s_at18823_s_at19382_at19897_s_at17303_s_at17916_at18339_at18844_at19401_at19903_at17305_at17917_s_at18365_s_at18859_at19402_at19905_at17318_at17918_at18402_at18864_at19406_at19906_at17323_at17926_s_at18439_s_at18880_at19413_at19907_at17374_at17935_at18487_at18883_g_at19416_at19910_at17405_at17956_i_at18508_s_at18886_at19429_at19920_s_at17415_at17961_at18512_at18892_s_at19432_s_at19932_at17418_s_at17966_at18543_at18909_s_at19439_at19951_at17420_at17978_s_at18552_at18911_at19448_s_at19962_at17423_s_at17986_s_at18567_at18913_s_at19454_at19963_at17426_at17993_at18573_at18916_s_at19462_s_at19969_at17427_at17998_s_at18580_at18921_g_at19464_at19970_s_at17430_s_at18003_at18581_at18950_at19469_at19972_at17431_at18005_at18584_at18951_s_at19483_at19981_at17439_g_at18010_s_at18587_s_at18956_at19484_s_at19990_at17442_i_at18013_r_at18590_at18966_at19513_at19996_at17449_s_at18023_s_at18591_at18972_at19548_at19999_s_at17462_s_at18029_g_at18592_s_at18994_at19563_s_at20009_s_at17463_at18030_i_at18600_at19030_at19567_at20013_at17465_at18045_at18601_s_at19039_at19581_at20017_at17475_at18046_s_at18607_s_at19068_i_at19595_s_at20018_at17479_at18059_i_at18610_s_at19108_at19606_at20024_s_at17495_s_at18064_r_at18611_at19115_at19623_at20045_at17508_s_at18065_r_at18616_at19117_s_at19627_s_at20047_at17522_s_at18074_at18622_g_at19122_at19636_at20048_at17523_s_at18076_s_at18628_at19125_s_at19641_at20050_at17529_s_at18077_at18631_at19127_at19652_at20051_at17537_s_at18078_at18636_at19135_at19655_at20058_at17539_s_at18081_at18638_at19144_at19658_at20067_at17543_s_at18083_r_at18652_at19157_s_at19660_at20069_at17555_s_at18085_r_at18657_at19158_at19665_s_at20099_at17557_s_at18091_at18667_at19177_at19667_at20100_at17560_s_at18154_s_at18675_at19192_at19690_s_at20113_s_at17564_s_at18165_at18684_at19198_at19695_at20123_at17565_s_at18174_at18686_s_at19222_at19717_at20127_s_at17568_at18221_at18688_s_at19226_g_at19726_s_at20129_at17570_g_at18226_s_at18693_s_at19227_at19752_s_at20133_i_at17573_at18230_at18698_s_at19230_at19759_at20152_at17577_g_at18237_at18706_s_at19232_s_at19782_at20154_at17578_at18255_at18707_at19263_at19789_s_at20173_at17579_s_at18257_at18726_s_at19285_at19803_s_at20178_s_at17585_s_at18258_s_at18727_at19332_at19828_at20183_at17596_at18274_s_at18732_i_at19346_at19831_i_at20188_at17600_s_at18275_at18735_s_at19347_at19833_s_at20189_at17823_s_at18278_at18736_at19361_s_at19834_at20197_at17840_s_at18283_at18738_f_at19362_at19835_at20200_at17849_s_at18290_at18747_f_at19363_at19841_at20210_g_at17857_at18291_at18754_at19364_at19867_at20213_at17865_at18299_s_at18782_at19365_s_at19870_s_at20229_at17882_at18300_at18789_at19373_at19871_at20232_s_at17885_at18306_at18806_s_at19379_at19872_at20255_at17902_s_at18327_s_at18814_at19381_at19876_at20278_s_at20284_at20693_at20288_g_at20701_s_at20294_at20704_at20312_s_at20707_s_at20331_at20719_at20335_s_at20350_s_at20354_s_at20355_at20369_s_at20378_g_at20383_at20385_s_at20387_at20399_at20409_g_at20420_at20429_s_at20439_at20440_at20444_at20445_at20449_at20474_at20480_s_at20495_s_at20499_at20501_at20516_at20520_s_at20530_s_at20538_s_at20547_at20558_at20561_at20567_at20571_at20590_at20592_at20594_at20608_s_at20612_s_at20616_at20620_g_at20635_s_at20637_at20643_at20654_s_at20670_at20674_s_at20684_at20685_at20689_s_at TABLE 7SALINE STRESS RESPONSIVE SEQUENCESSEQAFFYMETRIXID NO:ID NO:222712011_S_AT222812153_AT222912180_AT223012186_AT223112216_AT223212265_AT223312335_AT223412449_S_AT223512470_AT223612479_AT223712487_AT223812493_G_AT223912562_AT224012685_AT224112704_F_AT224212709_F_AT224312734_F_AT224412739_S_AT224512750_S_AT224612761_S_AT224712813_AT224812845_S_AT224912946_AT225013003_S_AT225113052_S_AT225213094_AT225313142_AT225413172_S_AT17880_S_AT225513198_I_AT225613209_S_AT16165_S_AT225713229_S_AT225813253_F_AT225913344_S_AT226013370_AT226113387_AT226213408_S_AT226313429_AT226413472_AT226513526_AT226613569_AT226713614_AT226813686_S_AT226913718_AT227013719_AT227113902_AT227213918_AT227313944_AT227413964_AT227513993_S_AT227614000_AT227714003_AT227814032_AT227914043_AT228014070_AT228114267_AT228214269_AT228314418_AT228414427_AT228514501_AT228614544_AT228714546_S_AT228814570_AT228914596_AT229014729_S_AT229114874_AT229214888_AT229314951_AT229414952_AT229514959_AT229614979_AT229715006_AT229815042_AT229915049_AT230015062_AT230115108_S_AT230215147_S_AT230315175_S_AT230415176_S_AT230515186_S_AT18696_S_AT230615192_S_AT230715208_S_AT230815324_AT230915371_AT231015424_AT231115463_AT231215465_AT231315497_S_AT231415589_S_AT231515636_S_AT231615663_S_AT231715770_AT231815792_AT231915855_AT232015860_AT232115891_AT232215898_AT232315909_AT232415965_AT232515969_S_AT232615975_S_AT232715995_S_AT232815998_S_AT18090_S_AT232916028_AT233016050_AT233116060_S_AT233216067_S_AT233316072_S_AT233416088_F_AT233516273_AT233616314_AT233716413_S_AT233816414_AT233916426_AT234016436_AT234116455_AT234216502_AT234316548_S_AT234416568_S_AT234516582_S_AT234616589_S_AT234716594_S_AT234816613_S_AT234916651_S_AT235016668_AT235116820_AT235216987_S_AT235316995_AT235417039_S_AT235517273_AT235617278_AT235717433_AT235817467_AT235917566_AT236017595_S_AT236117744_S_AT236217758_AT236317864_AT236417868_AT236517876_AT236617894_AT236717942_S_AT236818008_R_AT236918027_AT237018053_S_AT237118062_AT237218082_AT237318121_S_AT237418240_S_AT237518248_S_AT237618264_AT237718276_AT237818287_AT237918310_AT238018367_S_AT238118506_AT238218605_S_AT238318618_S_AT238418626_AT238518666_S_AT238618834_AT238718847_AT238818896_AT238918899_S_AT239018973_AT239118983_S_AT239218988_AT239318998_S_AT239419065_AT239519119_I_AT19121_AT239619207_AT239719220_AT239819284_AT239919315_AT240019348_AT240119403_S_AT240219437_S_AT240319502_AT240419609_AT240519645_AT240619742_AT240719863_AT240819873_AT240919891_AT241020004_S_AT241120053_AT241220138_AT241320193_AT241420199_AT241520220_AT241620239_G_AT241720297_AT241820324_S_AT241920353_AT242020362_AT242120389_AT242220546_AT242320600_AT242420623_AT242520629_AT242620648_S_AT242720668_AT TABLE 82X UP IN SALT, ONLY12037_at14570_at16190_at18506_at20648_s_at12137_at14578_s_at16196_at18605_s_at20678_at12153_at14596_at16273_at18626_at20686_at12186_at14646_s_at16314_at18666_s_at20707_s_at12216_at14662_f_at16413_s_at18747_f_at12268_at14668_s_at16414_at18782_at12449_s_at14729_s_at16417_s_at18834_at12470_at14874_at16455_at18847_at12476_at14888_at16548_s_at18913_s_at12487_at14918_at16582_s_at18973_at12493_g_at14952_at16589_s_at18988_at12609_at14959_at16594_s_at18998_s_at12685_at14986_at16613_s_at19065_at12704_f_at15006_at16651_s_at19068_i_at12709_f_at15042_at16668_at19123_at12734_f_at15047_at16690_g_at19177_at12739_s_at15062_at16762_at19220_at12750_s_at15063_at16820_at19284_at12761_s_at15108_s_at16873_i_at19288_at12819_at15133_s_at16987_s_at19315_at12845_s_at15147_s_at16989_at19437_s_at12946_at15170_s_at16995_at19484_s_at13142_at15175_s_at17039_s_at19502_at13198_i_at15182_s_at17040_s_at19503_at13229_s_at15190_s_at17400_s_at19592_at13275_f_at15192_s_at17425_s_at19645_at13344_s_at15324_at17433_at19742_at13370_at15392_at17467_at19835_at13408_s_at15424_at17490_s_at19873_at13464_at15467_at17529_s_at19891_at13472_at15497_s_at17543_s_at19992_at13526_at15581_s_at17566_at20004_s_at13614_at15623_f_at17595_s_at20053_at13652_at15636_s_at17744_s_at20133_i_at13679_s_at15646_s_at17758_at20138_at13751_at15670_s_at17855_at20190_at13918_at15770_at17864_at20199_at13919_at15775_at17876_at20200_at13944_at15778_at18008_r_at20297_at13964_at15792_at18013_r_at20324_s_at13987_s_at15855_at18024_s_at20335_s_at13993_s_at15891_at18027_at20353_at14000_at15909_at18053_s_at20362_at14032_at15923_at18078_at20385_s_at14043_at15969_s_at18082_at20389_at14052_at15975_s_at18090_s_at20402_s_at14067_at15995_s_at18091_at20450_at14070_at15998_s_at18121_s_at20468_at14269_at16017_at18264_at20489_at14285_at16050_at18276_at20546_at14427_at16067_s_at18300_at20569_s_at14501_at16072_s_at18367_s_at20600_at14540_at16165_s_at18471_at20623_at TABLE 92X UP SALT, 3 HR ONLY12037_at15042_at16987_s_at20004_s_at12137_at15047_at16989_at20053_at12153_at15062_at17039_s_at20133_i_at12186_at15063_at17040_s_at20138_at12216_at15108_s_at17425_s_at20190_at12268_at15133_s_at17433_at20199_at12470_at15147_s_at17490_s_at20200_at12476_at15170_s_at17543_s_at20220_at12487_at15175_s_at17744_s_at20362_at12493_g_at15182_s_at17864_at20385_s_at12609_at15190_s_at17876_at20389_at12685_at15192_s_at18008_r_at20489_at12704_f_at15324_at18013_r_at20546_at12709_f_at15424_at18024_s_at20623_at12734_f_at15467_at18027_at20648_s_at12739_s_at15497_s_at18053_s_at20678_at12750_s_at15623_f_at18078_at20707_s_at12819_at15636_s_at18082_at12946_at15646_s_at18090_s_at13142_at15670_s_at18091_at13229_s_at15770_at18121_s_at13275_f_at15775_at18264_at13370_at15778_at18276_at13408_s_at15792_at18367_s_at13464_at15855_at18471_at13472_at15891_at18506_at13614_at15909_at18605_s_at13652_at15923_at18626_at13679_s_at15969_s_at18666_s_at13918_at15975_s_at18747_f_at13919_at15995_s_at18782_at13944_at15998_s_at18834_at13987_s_at16017_at18847_at13993_s_at16050_at18913_s_at14000_at16067_s_at18973_at14032_at16072_s_at18988_at14043_at16165_s_at19065_at14052_at16196_at19068_i_at14067_at16273_at19123_at14269_at16314_at19177_at14285_at16414_at19220_at14501_at16417_s_at19288_at14540_at16455_at19315_at14570_at16548_s_at19437_s_at14596_at16582_s_at19484_s_at14668_s_at16589_s_at19502_at14729_s_at16594_s_at19503_at14888_at16613_s_at19592_at14918_at16651_s_at19645_at14952_at16668_at19742_at14959_at16762_at19835_at14986_at16820_at19873_at15006_at16873_i_at19891_at TABLE 102X DOWN SALT, ONLY12011_s_at16046_s_at20239_g_at12180_at16060_s_at20433_at12265_at16088_f_at20629_at12335_at16150_s_at20668_at12479_at16166_s_at12562_at16316_at12656_at16340_at12813_at16367_i_at13003_s_at16426_at13052_s_at16427_at13094_at16436_at13178_at16489_at13253_f_at16502_at13387_at16568_s_at13429_at16638_s_at13472_at16646_s_at13569_at17273_at13686_s_at17278_at13718_at17567_at13719_at17868_at13902_at17880_s_at14003_at17894_at14144_at17901_at14267_at17942_s_at14418_at17960_at14544_at17999_at14546_s_at18062_at14636_s_at18240_s_at14951_at18248_s_at14956_s_at18267_at14979_at18279_s_at14990_at18287_at15040_g_at18310_at15049_at18351_s_at15115_f_at18455_at15137_s_at18560_at15148_s_at18571_at15176_s_at18618_s_at15208_s_at18896_at15371_at18899_s_at15453_s_at18967_s_at15463_at18983_s_at15465_at19119_i_at15589_s_at19121_at15663_s_at19207_at15860_at19348_at15898_at19403_s_at15931_at19609_at15965_at19742_at15970_s_at19826_at15972_s_at19863_at16005_s_at19883_at16028_at20193_at TABLE 11OSMOTIC STRESS RESPONSIVE SEQUENCESSEQAFFYMETRIXID NO:ID NO:242811994_AT242912028_AT243012033_AT243112039_AT243212068_AT243312096_AT243412110_AT243512114_AT243612135_AT243712139_AT243812189_AT243912191_AT244012211_AT244112223_S_AT244212366_S_AT12869_S_AT244312381_AT244412406_S_AT244512412_AT244612453_AT244712571_S_AT244812662_AT244912746_I_AT245012774_AT245112787_AT245212847_AT245312848_AT245412895_AT245512911_S_AT245612920_AT12921_S_AT245713027_AT245813059_AT245913075_I_AT246013180_S_AT246113255_I_AT246213270_AT18167_S_AT246313283_S_AT246413382_AT246513386_S_AT246613433_AT246713482_AT246813732_AT246913733_I_AT247013842_AT247113860_S_AT247213868_AT247313901_AT247413933_AT247513995_AT247614062_AT247714118_I_AT247814141_AT247914310_AT248014354_AT248114476_AT248214513_S_AT248314568_S_AT248414604_AT248514634_S_AT248614660_S_AT248714666_S_AT248814686_S_AT17464_AT248914726_S_AT249014848_S_AT249114873_AT249214883_AT249315082_AT249415121_S_AT16014_S_AT249515168_S_AT249615271_AT249715338_AT249815418_AT249915429_AT250015548_AT250115666_S_AT250215672_S_AT250315680_S_AT250415867_AT250515918_AT250615999_S_AT250716303_AT250816363_AT250916440_S_AT251016458_S_AT251116475_AT251216513_S_AT251316529_AT251416547_S_AT251516553_F_AT251616563_S_AT251716629_S_AT251816797_AT251916814_AT252016832_AT252116976_S_AT252217007_AT252317037_S_AT252417054_S_AT252517257_S_AT18725_S_AT252617270_AT252717275_I_AT252817376_AT252917378_AT253017468_AT253117481_AT253217511_S_AT253317519_S_AT253417815_S_AT253517897_AT253617923_S_AT253717934_AT253817937_S_AT253917944_AT254017958_AT254118216_AT254218227_AT254318284_AT254418301_S_AT254518312_S_AT254618326_S_AT254718369_AT254818411_AT254918533_AT255018576_S_AT255118599_AT255218640_AT255318672_S_AT255418720_S_AT255518768_AT255618877_AT255718942_AT255818945_AT255918960_AT256018965_AT256119060_AT256219164_G_AT256319266_AT256419366_S_AT256519369_AT256619371_AT256719386_AT256819412_AT256919427_S_AT257019622_G_AT257119681_AT257219819_S_AT257319961_S_AT257420002_AT257520034_I_AT257620062_AT257720136_AT257820223_AT257920235_I_AT258020401_AT258120407_AT258220470_AT258320626_AT258420631_S_AT258520647_AT TABLE 122X UP IN MANNITOL, ONLY12039_at16832_at12068_at16993_at12139_at17037_s_at12212_at17054_s_at12278_at17083_s_at12366_s_at17097_s_at12453_at17119_s_at12556_at17270_at12575_s_at17305_at12746_i_at17376_at12848_at17378_at12869_s_at17449_s_at12920_at17481_at12921_s_at17533_s_at13041_s_at17832_s_at13059_at17923_s_at13241_s_at17944_at13255_i_at18059_f_at13270_at18216_at13382_at18230_at13406_at18255_at13433_at18284_at13550_at18301_s_at13672_s_at18312_s_at13716_at18326_s_at13842_at18599_at13933_at18672_s_at13995_at18720_s_at14062_at18768_at14075_at18814_at14162_at18877_at14208_at18921_g_at14217_at18960_at14235_at19060_at14310_at19182_at14431_at19192_at14513_s_at19266_at14584_at19369_at14604_at19386_at14673_s_at19402_at14856_s_at19412_at15207_s_at19432_s_at15338_at19469_at15406_at19622_g_at15418_at19819_s_at15591_s_at19826_at15666_s_at20152_at15680_s_at20223_at15866_s_at20235_i_at15918_at20365_s_at16340_at20470_at16553_f_at20537_at16797_at20547_at TABLE 132X UP IN MANNITOL, 3 HR ONLY12039_at17449_s_at12068_at17481_at12139_at17533_s_at12212_at17923_s_at12278_at17944_at12366_s_at18059_i_at12453_at18216_at12556_at18230_at12575_s_at18255_at12746_i_at18301_s_at12848_at18312_s_at12869_s_at18326_s_at12920_at18599_at12921_s_at18720_s_at13041_s_at18768_at13059_at18814_at13241_s_at18877_at13382_at18921_g_at13406_at18960_at13433_at19060_at13550_at19192_at13672_s_at19266_at13933_at19369_at13995_at19386_at14062_at19402_at14075_at19412_at14162_at19432_s_at14217_at19469_at14310_at19622_g_at14431_at19819_s_at14513_s_at20152_at14584_at20223_at14604_at20235_i_at14673_s_at20365_s_at14856_s_at20470_at15207_s_at20537_at15338_at15418_at15591_s_at15866_s_at15918_at16340_at16553_f_at16797_at16832_at17037_s_at17054_s_at17083_s_at17097_s_at17270_at17305_at17376_at17378_at TABLE 142X DOWN IN MANNITOL, ONLY12028_at14897_at17958_at12033_at14918_at18012_s_at12110_at15082_at18227_at12114_at15084_at18272_at12189_at15098_s_at18331_s_at12191_at15105_s_at18369_at12211_at15121_s_at18411_at12223_s_at15126_s_at18533_at12268_at15168_s_at18576_s_at12345_at15271_at18640_at12381_at15429_at18696_s_at12406_s_at15548_at18945_at12412_at15672_s_at18949_at12522_at15753_at18953_at12571_s_at15867_at18965_at12662_at15999_s_at19164_g_at12787_at16001_at19322_at12847_at16021_s_at19366_s_at12895_at16190_at19371_at12911_s_at16260_at19397_at13027_at16303_at19427_s_at13075_i_at16363_at19681_at13221_at16458_s_at19707_s_at13262_s_at16468_at19839_at13283_s_at16475_at19961_s_at13386_s_at16513_s_at19976_at13447_s_at16529_at19998_at13482_at16563_s_at20002_at13634_s_at16690_g_at20034_i_at13709_s_at16814_at20136_at13732_at16847_at20382_s_at13733_i_at16927_s_at20407_at13812_s_at16976_s_at20529_at13825_s_at17007_at20626_at13860_s_at17014_s_at20631_s_at13868_at17016_s_at20647_at13901_at17071_s_at20699_at14052_at17090_s_at14224_at17257_s_at14244_s_at17275_i_at14254_s_at17424_at14256_f_at17464_at14354_at17468_at14476_at17511_s_at14568_s_at17519_s_at14634_s_at17525_s_at14646_s_at17645_s_at14660_s_at17741_at14686_s_at17815_s_at14726_s_at17897_at14848_s_at17899_at14873_at17934_at14883_at17937_s_at TABLE 15COLD & OSOMOTIC STRESS RESPONSIVE SEQUENCESSEQAFFYMETRIXID NO:ID NO:169912040_AT170012048_AT170112054_S_AT170212077_AT170312107_I_AT170412113_AT170512154_AT170612171_AT170712212_AT170812278_AT170912317_AT171012325_AT171112333_AT171212345_AT171312349_S_AT14254_S_AT14256_F_AT171412356_AT171512380_AT171612392_AT171712460_S_AT171812556_AT171912575_S_AT172012686_S_AT172112701_I_AT172212754_G_AT172312782_R_AT172412784_AT172512879_S_AT172612891_AT16817_S_AT172712898_G_AT172812974_AT172912998_AT173013041_S_AT173113124_AT173213134_S_AT173313144_AT173413147_AT173513152_S_AT173613187_I_AT16981_S_AT173713192_S_AT17525_S_AT173813212_S_AT173913215_S_AT16649_S_AT174013241_S_AT174113246_AT174213262_S_AT174313286_S_AT174413324_AT174513340_S_AT174613361_AT174713406_AT174813441_S_AT174913513_AT175013550_AT175113573_AT175213577_S_AT175313606_AT175413609_AT175513625_S_AT175613626_AT175713634_S_AT175813672_S_AT18916_S_AT175913709_S_AT176013736_AT176113775_AT176213810_AT176313812_S_AT176413825_S_AT176514015_S_AT14016_S_AT176614029_AT176714036_AT176814051_AT176914060_AT177014064_AT177114066_AT177214075_AT177314094_S_AT19999_S_AT177414096_AT177514104_AT177614123_S_AT177714126_S_AT177814131_AT177914136_AT178014139_AT14140_AT178114162_AT14217_AT178214178_AT178314201_AT178414208_AT178514235_AT178614242_S_AT178714431_AT178814480_AT178914497_AT179014553_AT179114584_AT179214600_AT179314673_S_AT19432_S_AT179414681_G_AT179514699_AT179614751_AT179714762_AT179814828_S_AT179914856_S_AT180014882_AT180114897_AT180214978_AT180314985_S_AT180415031_AT180515084_AT180615096_AT180715105_S_AT180815110_S_AT180915111_S_AT181015120_S_AT181115126_S_AT181215142_S_AT181315144_S_AT181415184_S_AT181515198_S_AT181615203_S_AT181715207_S_AT181815240_AT181915366_AT182015398_AT182115406_AT182215448_AT182315466_AT182415481_AT182515484_AT182615549_AT182715591_S_AT182815606_S_AT182915614_S_AT16927_S_AT183015629_S_AT183115633_S_AT183215641_S_AT18012_S_AT183315720_AT183415815_S_AT183515817_AT183615837_AT183715841_AT183815866_S_AT18255_AT183915872_AT18331_S_AT184015892_AT184115933_AT184215947_AT184315959_S_AT184416001_AT184516052_AT184616161_S_AT184716204_AT184816232_S_AT184916252_AT185016260_AT185116266_AT185216299_AT185316365_AT185416468_AT185516477_AT185616491_AT185716523_S_AT185816566_S_AT185916570_S_AT186016688_AT186116840_AT186216847_AT186316893_AT186416896_S_AT186516898_S_AT186616912_S_AT186716980_AT186816993_AT186917008_AT187017012_S_AT187117014_S_AT187217016_S_AT187317032_S_AT187417050_S_AT17051_S_AT187517071_S_AT187617090_S_AT18690_S_AT187717097_S_AT187817104_S_AT187917119_S_AT188017160_AT188117305_AT188217424_AT188317449_S_AT188417452_G_AT188517540_S_AT188617552_S_AT188717571_AT188817589_AT188917641_G_AT189017741_AT18098_AT189117766_AT189217873_S_AT189317904_AT189417920_S_AT189517925_AT189617943_AT189718059_I_AT189818230_AT189918263_AT190018272_AT190118540_AT190218608_AT190318647_AT190418662_S_AT190518664_AT190618695_S_AT190718704_AT190818814_AT190918907_S_AT191018921_G_AT191118924_AT191218949_AT19707_S_AT191318995_AT191419017_AT191519034_AT191619063_AT191719142_AT191819158_AT191919180_AT192019187_AT192119192_AT192219195_AT192319199_AT192419231_AT192519263_AT192619308_AT192719322_AT192819365_S_AT192919372_AT193019389_AT193119392_AT193219397_AT193319400_AT193419402_AT193519458_AT193619469_AT193719473_AT193819597_S_AT193919710_S_AT194019830_AT194119839_AT194219840_S_AT194319853_AT194419860_AT194519880_AT194619889_AT194719898_AT194819914_AT194919924_AT195019949_AT195119976_AT195219998_AT195320030_AT195420151_AT195520152_AT195620187_AT195720214_I_AT195820269_AT195920271_AT196020273_AT196120299_AT196220323_AT196320429_S_AT196420457_AT196520480_S_AT196620529_AT196720547_AT196820555_S_AT196920699_AT TABLE 162X UP IN MANNITOL & COLD, ONLY12345_at17066_s_at12784_at17540_s_at13153_r_at17567_at13212_s_at17766_at13215_s_at17904_at13246_at17920_s_at13262_s_at17943_at13361_at18263_at13625_s_at18351_s_at13764_at18662_s_at13810_at18670_g_at14015_s_at18695_s_at14016_s_at18704_at14060_at18729_at14096_at18995_at14123_s_at19158_at14139_at19473_at14219_at19710_s_at14248_at19883_at14254_s_at19889_at14256_f_at20030_at14609_at20269_at14636_s_at20271_at14681_g_at20299_at14699_at20429_s_at14704_s_at20438_at14828_s_at20480_s_at14882_at15110_s_at15184_s_at15448_at15629_s_at15720_at15846_at15947_at16161_s_at16365_at16427_at16566_s_at16570_s_at16649_s_at16688_at16712_at16817_s_at16840_at16893_at16912_s_at16916_s_at16927_s_at16981_s_at17012_s_at17014_s_at17051_s_at TABLE 172X DOWN COLD & MANNITOL, ONLY12040_at14553_at17873_s_at12048_at14612_at17925_at12054_s_at14751_at18098_at12077_at14762_at18540_at12107_i_at14978_at18608_at12113_at14985_s_at18647_at12154_at15031_at18664_at12171_at15096_at18690_s_at12317_at15111_s_at18725_s_at12325_at15120_s_at18924_at12333_at15142_s_at19017_at12356_at15198_s_at19034_at12380_at15203_s_at19063_at12392_at15240_at19141_at12460_s_at15366_at19142_at12686_s_at15392_at19180_at12701_i_at15398_at19187_at12782_r_at15466_at19195_at12879_s_at15481_at19199_at12898_g_at15484_at19231_at12974_at15549_at19308_at12998_at15623_f_at19372_at13144_at15815_s_at19392_at13147_at15817_at19400_at13152_s_at15841_at19458_at13192_s_at15892_at19597_s_at13286_s_at15933_at19762_at13324_at15959_s_at19830_at13340_s_at16052_at19853_at13441_s_at16204_at19869_at13513_at16252_at19880_at13573_at16266_at19898_at13606_at16299_at19914_at13609_at16477_at19924_at13626_at16491_at19949_at13736_at16561_s_at20151_at13775_at16645_s_at20187_at14029_at16898_s_at20214_i_at14036_at16980_at20273_at14051_at17008_at20323_at14064_at17104_s_at20457_at14066_at17160_at20555_s_at14094_s_at17317_at14104_at17400_s_at14126_s_at17452_g_at14131_at17477_s_at14136_at17500_s_at14178_at17552_s_at14192_at17571_at14201_at17572_s_at14242_s_at17589_at14480_at17641_g_at14497_at17855_at TABLE 18COLD & SALINE STRESS RESPONSIVE SEQUENCESSEQAFFYMETRIXID NO:ID NO:197012021_AT197112037_AT197212094_AT197312098_AT197412128_AT197512148_AT197612151_AT197712357_S_AT197812394_AT197912472_S_AT198012475_AT198112482_S_AT198212490_AT198312505_S_AT198412531_AT198512540_S_AT198612541_AT198712577_AT198812594_AT198912629_AT199012642_AT199112656_AT199212660_AT199312712_F_AT199412725_R_AT199512745_AT199612777_I_AT199712790_S_AT199812798_AT199912801_AT200012855_F_AT200112887_S_AT200212933_R_AT200312951_AT200413005_AT200513015_S_AT200613115_AT200713178_AT200813228_AT200913236_S_AT16646_S_AT201013266_S_AT15211_S_AT201113275_F_AT201213335_AT201313362_S_AT201413428_AT201513464_AT201613480_AT201713538_AT201813544_AT201913549_AT202013565_AT202113580_AT202213588_AT202313649_AT202413652_AT202513679_S_AT202613696_AT202713702_S_AT202813751_AT202913919_AT203013943_AT203113950_S_AT203214050_AT203314055_S_AT16166_S_AT203414067_AT203514078_AT203614110_I_AT203714144_AT203814232_AT203914285_AT204014346_AT204114432_AT204214468_AT204314479_AT204414524_S_AT204514608_AT204614621_AT204714635_S_AT17128_S_AT204814640_S_AT204914643_S_AT205014663_S_AT205114668_S_AT205214688_S_AT18279_S_AT205314737_S_AT205414768_AT205514875_AT205614911_S_AT17056_S_AT205714924_AT205814956_S_AT15148_S_AT18673_AT205914964_AT206015022_AT206115040_G_AT206215047_AT206315063_AT206415085_S_AT206515123_S_AT206615133_S_AT206715137_S_AT206815153_S_AT206915170_S_AT207015172_S_AT207115182_S_AT207215190_S_AT207315241_S_AT207415389_AT207515453_S_AT207615495_AT207715496_AT207815519_S_AT207915562_AT208015580_S_AT208115582_S_AT208215638_S_AT18751_F_AT208315646_S_AT208415647_S_AT208515654_S_AT208615655_S_AT208715658_S_AT208815670_S_AT208915775_AT209015798_AT209115930_AT209215931_AT209315949_S_AT209416017_AT209516053_I_AT209616078_S_AT209716086_S_AT209816120_S_AT209916126_S_AT210016150_S_AT210116159_S_AT210216230_AT210316306_AT210416367_I_AT210516417_S_AT18083_R_AT210616418_S_AT210716423_AT210816449_S_AT210916484_S_AT211016489_AT211116565_S_AT211216596_S_AT211316600_S_AT211416603_S_AT211516638_S_AT211616642_S_AT211716763_AT211816914_S_AT211916968_AT212016983_AT212116989_AT212217002_AT212317015_S_AT212417040_S_AT18913_S_AT212517232_AT212617380_AT212717394_S_AT20640_S_AT212817398_AT212917448_AT213017485_S_AT213117490_S_AT213217499_S_AT213317505_S_AT213417516_S_AT213517529_S_AT213617543_S_AT213717593_R_AT19858_S_AT213817609_AT213917698_AT214017836_AT214117886_AT214217896_AT214317901_AT214417902_S_AT214517913_S_AT214617924_AT214717954_S_AT214817960_AT214917991_G_AT18967_S_AT215017999_AT215118057_I_AT215218078_AT215318091_AT215418168_S_AT215518252_AT215618267_AT215718300_AT215818308_I_AT215918328_AT216018354_AT216118402_AT216218416_AT216318455_AT216418459_AT216518571_AT216618604_AT19181_S_AT216718644_AT216818745_F_AT19611_S_AT216918782_AT217018881_AT217118904_S_AT217218914_S_AT217318963_AT217419068_I_AT217519078_AT217619171_AT217719177_AT217819394_AT217919411_AT218019415_AT218119466_S_AT218219484_S_AT218319549_S_AT218419592_AT218519633_AT218619641_AT218719669_AT218819672_AT218919684_AT219019692_AT219119746_AT219219835_AT219319848_S_AT219419892_AT219519904_AT219619936_AT219719974_S_AT219819994_AT219920005_S_AT220020022_AT220120032_AT220220044_AT220320049_AT220420081_AT220520133_I_AT220620155_S_AT220720163_S_AT220820200_AT220920296_S_AT221020336_AT221120341_AT221220372_AT221320385_S_AT221420433_AT221520489_AT221620525_AT221720543_AT221820565_AT221920570_AT222020576_AT222120577_AT222220609_AT222320646_AT222420672_AT222520707_S_AT222620720_AT TABLE 192X UP IN SALT & COLD, ONLY12004_at12098_at12148_at12251_at12357_s_at12394_at12457_at12505_s_at12522_at12541_at12594_at12606_at12697_at12745_at12781_at12798_at12855_f_at12945_at12951_at13005_at13015_s_at13115_at13146_s_at13335_at13447_s_at13480_at13544_at13549_at13580_at13649_at13943_at13950_s_at14110_i_at14144_at14224_at14432_at14468_at14479_at14524_s_at14640_s_at14643_s_at14735_s_at14737_s_at14768_at14784_at14924_at15064_at15127_s_at15186_s_at15189_s_at15255_at15389_at15482_at15495_at15496_at15519_s_at15580_s_at15582_s_at15776_at15798_at15910_at15931_at15937_at15949_s_at15972_s_at16048_at16086_s_at16120_s_at16126_s_at16150_s_at16159_s_at16230_at16306_at16418_s_at16423_at16449_s_at16565_s_at16603_s_at16763_at16968_at16983_at17002_at17015_s_at17019_s_at17078_s_at17232_at17317_at17394_s_at17516_s_at17585_s_at17609_at17698_at17836_at17896_at17899_at17902_s_at17960_at17963_at18168_s_at18252_at18267_at18308_i_at18354_at18402_at18459_at18484_at18745_f_at18904_s_at18914_s_at18929_s_at18946_at18963_at19078_at19137_at19141_at19411_at19641_at19672_at19684_at19692_at19746_at19762_at19869_at19894_at19904_at19936_at19994_at20005_s_at20031_at20044_at20382_s_at20406_g_at20421_at20525_at20543_at20565_at20570_at20640_s_at20646_at20720_at TABLE 202X DOWN IN COLD & SALT, ONLY12021_at15123_s_at19394_at12094_at15153_s_at19415_at12128_at15172_s_at19466_s_at12151_at15190_s_at19549_s_at12332_s_at15211_s_at19592_at12472_s_at15241_s_at19633_at12475_at15437_at19669_at12482_s_at15562_at19848_s_at12490_at15638_s_at19858_s_at12531_at15647_s_at19878_at12540_s_at15654_s_at19892_at12577_at15655_s_at19974_s_at12629_at15658_s_at20022_at12642_at15695_s_at20032_at12660_at15846_at20049_at12676_s_at15930_at20081_at12712_f_at16053_i_at20155_s_at12725_r_at16078_s_at20163_s_at12777_i_at16229_at20296_s_at12790_s_at16465_at20336_at12801_at16484_s_at20341_at12887_s_at16596_s_at20365_s_at12933_r_at16600_s_at20372_at13153_r_at16642_s_at20489_at13228_at16914_s_at20491_at13362_s_at17027_s_at20576_at13428_at17066_s_at20577_at13538_at17083_s_at20609_at13565_at17128_s_at20672_at13588_at17380_at13696_at17398_at13702_s_at17448_at13716_at17485_s_at13764_at17490_s_at14050_at17499_s_at14055_s_at17505_s_at14069_at17514_s_at14078_at17593_r_at14232_at17886_at14346_at17913_s_at14608_at17924_at14609_at17954_s_at14621_at17991_g_at14635_s_at18057_i_at14663_s_at18069_at14688_s_at18328_at14691_at18416_at14704_s_at18604_at14875_at18644_at14911_s_at18881_at14964_at19171_at15022_at19181_s_at15085_s_at19182_at TABLE 21OSMOTIC & SALINE STRESS RESPONSIVE SEQUENCESSEQAFFYMETRIXID NO:ID NO:258612126_S_AT258712137_AT258812227_AT258912239_AT259012268_AT259112369_AT259212476_AT259312484_G_AT259412494_AT259512644_AT259612645_AT259712796_S_AT259812819_AT259912841_AT260012852_S_AT19455_S_AT260113084_AT260213171_AT260313174_R_AT260413596_AT260513807_AT260613977_AT260713999_AT260814052_AT260914293_AT261014335_AT261114486_AT261214506_AT261314518_AT261414540_AT261514578_S_AT261614646_S_AT261714662_F_AT15962_S_AT261814901_AT261914918_AT262014986_AT262115053_S_AT262215179_S_AT262315252_G_AT262415280_AT262515467_AT262615607_S_AT262715625_S_AT262815703_I_AT262915827_AT263015863_AT263115923_AT263215946_S_AT263316005_S_AT263416073_F_AT263516114_S_AT263616127_S_AT18744_F_AT263716190_AT263816196_AT263916236_G_AT19531_AT264016310_AT264116316_AT264216334_S_AT264316335_AT264416340_AT264516450_S_AT264616500_AT264716524_AT264816533_AT264916690_G_AT265016762_AT265116819_AT265216873_I_AT265316972_AT265416991_AT265517099_S_AT265617339_AT265717397_S_AT265817419_AT265917460_AT266017554_S_AT266117939_AT266218013_R_AT18178_S_AT266318024_S_AT266418032_I_AT266518054_AT266618151_AT266718281_AT266818445_AT266918520_AT267018583_AT267118663_S_AT267218753_S_AT267318876_AT267418938_G_AT267518971_AT267618977_AT267718981_AT267819099_AT267919196_AT268019376_AT268119409_AT268219503_AT268319826_AT268419847_S_AT268519930_AT268619992_AT268720096_AT268820108_AT268920256_S_AT269020290_S_AT269120298_AT269220305_AT269320322_AT269420333_AT269520402_S_AT269620424_AT269720446_S_AT269820450_AT269920468_AT270020569_S_AT270120639_AT270220678_AT270320686_AT TABLE 222X UP IN SALT & MANNITOL, ONLY12126_s_at17548_s_at12227_at17554_s_at12369_at17961_at12521_at18032_i_at12644_at18054_at12645_at18151_at12724_f_at18167_s_at12795_at18281_at12796_s_at18520_at12841_at18663_s_at12852_s_at18744_f_at12958_at18753_s_at13014_at18789_at13174_r_at18876_at13211_s_at18909_s_at13596_at18938_g_at13640_at18977_at13789_at19099_at13977_at19108_at13999_at19135_at14069_at19227_at14083_at19376_at14089_at19429_at14293_at19455_s_at14675_s_at19531_at15053_s_at19789_s_at15058_s_at19878_at15252_g_at20017_at15280_at20096_at15437_at20256_s_at15607_s_at20290_s_at15625_s_at20305_at15827_at20322_at15863_at20333_at15880_at20420_at16005_s_at20424_at16031_at20689_s_at16073_f_at16316_at16334_s_at16335_at16450_s_at16500_at16524_at16533_at16597_s_at16819_at17085_s_at17099_s_at17339_at17419_at17442_i_at17514_s_at TABLE 232X DOWN IN MANNITOL & SALT, ONLY12239_at20108_at12251_at20298_at12476_at20421_at12484_g_at20432_at12494_at20446_s_at12561_at20639_at12647_s_at12719_f_at12819_at12841_at13084_at13171_at13172_s_at13435_at13807_at14250_r_at14335_at14486_at14506_at14518_at14901_at15046_s_at15179_s_at15451_at15703_i_at15946_s_at16014_s_at16114_s_at16310_at16342_at16712_at16762_at16972_at16991_at17397_s_at17408_at17460_at17775_at17939_at18445_at18583_at18751_f_at18971_at18981_at19156_s_at19196_at19359_s_at19409_at19503_at19713_at19718_at19847_s_at19930_at TABLE 24COLD, OSMOTIC & SALINE RESPONSIVE SEQUENCESSEQAFFYMETRIXID NO:ID NO:126212004_AT126312023_S_AT126412078_AT126512115_AT126612118_AT126712150_AT126812251_AT126912271_S_AT127012276_AT127112332_S_AT13211_S_AT127212338_AT127312400_AT127412430_AT127512457_AT127612521_AT127712522_AT127812530_AT127912536_S_AT128012538_AT128112561_AT128212574_AT19019_I_AT128312595_AT128412606_AT128512609_AT128612622_AT128712630_AT128812647_S_AT128912676_S_AT129012697_AT129112698_AT129212719_F_AT129312724_F_AT15871_S_AT16597_S_AT129412749_AT129512765_AT129612769_AT129712781_AT129812785_AT129912792_S_AT130012795_AT130112805_S_AT130212857_AT130312883_S_AT130412909_S_AT16539_S_AT130512932_S_AT15605_S_AT130612945_AT130712958_AT130812964_AT130912968_AT131012972_AT131112989_S_AT131213004_AT131313014_AT131413025_AT131513036_AT131613099_S_AT131713136_AT131813146_S_AT13239_S_AT131913153_R_AT132013159_AT132113176_AT132213217_S_AT17500_S_AT132313225_S_AT15997_S_AT132413230_S_AT15972_S_AT132513279_S_AT17477_S_AT132613280_S_AT20301_S_AT132713282_S_AT17027_S_AT132813426_AT132913432_AT133013435_AT133113447_S_AT133213474_AT133313511_AT133413546_AT133513547_S_AT133613548_AT133713555_AT133813587_AT133913595_AT134013610_S_AT134113627_AT134213640_AT134313645_AT134413647_AT134513706_S_AT19701_S_AT134613716_AT18228_AT134713725_AT134813764_AT134913771_AT135013789_AT135113916_AT135213965_S_AT135313967_AT135414028_AT135514039_AT135614046_AT135714049_AT135814069_AT135914077_AT136014080_AT136114083_AT136214089_AT136314090_I_AT136414097_AT136514116_AT136614151_AT14219_AT136714170_AT136814172_AT136914192_AT137014224_AT137114227_AT137214244_S_AT14245_AT14645_S_AT15974_G_AT137314248_AT137414250_R_AT137514367_AT137614381_AT137714384_AT137814398_S_AT137914487_AT138014582_AT138114597_AT138214609_AT138314612_AT19267_S_AT138414614_AT138514636_S_AT138614644_S_AT14658_S_AT14659_S_AT15964_S_AT138714675_S_AT138814691_AT14709_AT138914704_S_AT15846_AT139014705_I_AT139114733_S_AT139214735_S_AT139314779_AT139414784_AT139514923_AT139614947_AT139714950_AT139814990_AT139914998_AT140015005_S_AT140115018_AT140215045_AT140315046_S_AT140415052_AT140515058_S_AT140615064_AT140715088_S_AT140815098_S_AT140915103_S_AT141015109_S_AT141115124_S_AT141215127_S_AT141315145_S_AT141415154_S_AT141515161_S_AT141615189_S_AT141715214_S_AT141815255_AT141915356_AT142015357_AT142115364_AT142215392_AT142315403_S_AT142415437_AT142515451_AT142615476_AT142715482_AT142815483_S_AT142915521_S_AT143015522_I_AT143115531_I_AT143215573_AT143315581_S_AT143415586_S_AT143515594_S_AT143615609_S_AT143715611_S_AT143815621_F_AT143915623_F_AT144015669_S_AT144115695_S_AT144215702_S_AT144315753_AT144415761_AT144515776_AT144615778_AT144715839_AT144815842_AT144915857_S_AT145015859_AT145115880_AT145215886_AT145315906_S_AT145415910_AT145515937_AT145615957_AT145715970_S_AT145815985_AT145916010_S_AT16011_S_AT17078_S_AT146016021_S_AT146116031_AT146216038_S_AT146316045_S_AT146416046_S_AT146516048_AT146616061_S_AT146716082_S_AT146816111_F_AT146916115_S_AT147016141_S_AT147116144_S_AT147216163_S_AT147316173_S_AT147416229_AT147516298_AT147616301_S_AT147716322_AT147816342_AT147916351_AT148016412_S_AT148116422_AT148216427_AT148316438_AT148416474_S_AT148516482_S_AT148616485_S_AT18052_S_AT148716493_AT148816534_S_AT148916555_S_AT149016561_S_AT17572_S_AT149116592_S_AT149216615_S_AT149316637_S_AT149416692_AT149516712_AT149616789_AT149716818_S_AT149816971_S_AT149917018_S_AT150017019_S_AT150117029_S_AT150217041_S_AT150317047_S_AT150417066_S_AT150517085_S_AT150617089_S_AT150717179_AT150817180_AT150917228_AT151017252_AT151117317_AT151217338_AT151317384_AT151417387_S_AT151517400_S_AT151617407_S_AT151717408_AT151817413_S_AT151917416_AT152017425_S_AT152117440_I_AT152217442_I_AT152317473_AT152417484_AT152517514_S_AT152617520_S_AT152717533_S_AT152817548_S_AT19614_AT152917549_S_AT153017555_S_AT153117567_AT153217654_AT153317693_AT153417697_AT153517722_AT153617752_AT153717755_AT153817775_AT153917832_S_AT154017840_S_AT154117843_S_AT154217855_AT154317860_AT154417869_AT154517888_AT154617899_AT154717929_S_AT154817930_S_AT154917932_S_AT155017936_S_AT18670_G_AT155117957_AT155217961_AT155317962_AT155417963_AT155517971_S_AT155617975_AT18742_F_AT155718016_R_AT155818069_AT155918122_AT156018140_AT156118199_AT156218224_S_AT156318225_AT156418235_AT156518259_S_AT156618265_AT156718270_AT156818280_AT156918289_AT157018296_AT157118298_AT157218314_I_AT157318318_AT157418325_AT157518351_S_AT157618471_AT157718482_S_AT157818484_AT157918560_AT158018564_AT158118590_AT158218594_AT158318595_AT158418596_AT158518629_S_AT158618637_AT158718661_AT158818668_AT158918699_I_AT159018747_F_AT18789_AT159118761_AT159218833_AT159318875_S_AT159418894_AT159518936_AT159618946_AT159718953_AT159818955_AT159918972_AT160019008_S_AT160119108_AT160219123_AT160319135_AT160419137_AT160519141_AT160619152_AT160719156_S_AT160819182_AT160919186_S_AT161019214_AT161119216_AT161219227_AT161319243_AT161419288_AT161519359_S_AT161619368_AT161719379_AT161819380_S_AT161919398_AT162019421_AT162119424_AT162219429_AT162319430_AT162419450_AT162519457_AT162619467_AT162719516_AT162819545_AT162919564_AT163019577_AT163119593_AT163219602_AT163319618_AT163419638_AT163519640_AT163619646_S_AT163719656_S_AT163819670_AT163919696_AT164019713_AT164119718_AT164219722_S_AT164319749_AT164419755_AT164519762_AT164619789_S_AT164719815_AT164819843_AT164919869_AT165019878_AT165119883_AT165219894_AT165319926_AT165419944_AT165519968_AT165619977_AT165719982_AT165819987_AT165919991_AT166020015_AT166120017_AT166220031_AT166320040_AT166420042_S_AT166520060_AT20438_AT166620089_AT166720118_AT166820144_AT166920149_AT167020179_AT167120190_AT167220194_AT167320219_AT167420245_S_AT167520263_AT167620308_S_AT167720335_S_AT167820338_AT167920345_AT168020365_S_AT168120382_S_AT168220390_S_AT168320395_AT168420420_AT168520421_AT168620432_AT168720437_AT168820442_I_AT168920463_S_AT169020491_AT169120537_AT169220573_AT169320636_AT169420638_AT169520641_AT169620658_S_AT169720689_S_AT169820698_S_AT TABLE 252X UP IN COLD, SALT & MANNITOL12023_s_at14733_s_at17047_s_at19640_at12332_s_at14923_at17179_at19646_s_at12530_at14990_at17180_at19656_s_at12536_s_at15005_s_at17252_at19701_s_at12574_at15018_at17384_at19843_at12595_at15052_at17407_s_at19944_at12698_at15088_s_at17484_at19982_at12749_at15098_s_at17520_s_at19987_at12765_at15103_s_at17555_s_at19991_at12769_at15145_s_at17572_s_at20042_s_at12785_at15154_s_at17722_at20060_at12857_at15161_s_at17752_at20118_at12964_at15214_s_at17840_s_at20144_at12972_at15356_at17843_s_at20149_at12989_s_at15521_s_at17860_at20179_at13004_at15573_at17929_s_at20194_at13025_at15586_s_at17936_s_at20245_s_at13036_at15609_s_at17962_at20390_s_at13099_s_at15611_s_at18052_s_at20437_at13136_at15621_f_at18069_at20463_s_at13176_at15669_s_at18122_at20491_at13220_s_at15695_s_at18199_at20641_at13225_s_at15753_at18259_s_at20658_s_at13230_s_at15761_at18280_at13239_s_at15857_s_at18289_at13426_at15871_s_at18314_i_at13474_at15964_s_at18318_at13548_at15970_s_at18325_at13555_at15974_g_at18482_s_at13595_at15997_s_at18590_at13627_at16011_s_at18594_at13645_at16021_s_at18595_at13647_at16038_s_at18596_at13706_s_at16046_s_at18629_s_at13965_s_at16082_s_at18661_at13967_at16111_f_at18668_at14080_at16115_s_at18699_i_at14090_i_at16127_s_at18722_s_at14097_at16141_s_at18936_at14116_at16144_s_at18953_at14151_at16163_s_at18955_at14172_at16236_g_at18972_at14192_at16301_s_at19008_s_at14244_s_at16322_at19152_at14245_at16422_at19186_s_at14367_at16474_s_at19214_at14398_s_at16482_s_at19368_at14582_at16485_s_at19379_at14614_at16555_s_at19380_s_at14644_s_at16561_s_at19421_at14645_s_at16592_s_at19545_at14658_s_at16637_s_at19614_at14659_s_at17041_s_at19638_at TABLE 262X DOWN IN COLD, MANNITOL & SALT, ONLY12078_at15189_s_at17869_at20015_at12115_at15357_at17888_at20040_at12118_at15364_at17930_s_at20089_at12150_at15403_s_at17932_s_at20190_at12271_s_at15476_at17957_at20219_at12276_at15483_s_at17963_at20263_at12338_at15522_i_at17971_s_at20301_s_at12400_at15531_i_at17975_at20308_s_at12430_at15594_s_at18016_r_at20338_at12538_at15702_s_at18140_at20345_at12622_at15778_at18224_s_at20395_at12630_at15839_at18225_at20442_i_at12792_s_at15842_at18228_at20537_at12805_s_at15859_at18235_at20573_at12883_s_at15872_at18265_at20636_at12909_s_at15880_at18270_at20638_at12932_s_at15886_at18296_at20698_s_at12968_at15906_s_at18298_at13159_at15957_at18471_at13217_s_at15985_at18564_at13279_s_at16045_s_at18637_at13282_s_at16061_s_at18742_f_at13432_at16173_s_at18761_at13511_at16298_at18833_at13546_at16351_at18875_s_at13547_s_at16412_s_at18894_at13587_at16438_at18946_at13610_s_at16493_at19123_at13640_at16534_s_at19216_at13725_at16539_s_at19243_at13771_at16615_s_at19267_s_at13916_at16692_at19288_at14028_at16789_at19398_at14039_at16818_s_at19424_at14046_at16971_s_at19430_at14049_at17018_s_at19450_at14077_at17029_s_at19457_at14170_at17089_s_at19467_at14227_at17228_at19516_at14248_at17338_at19564_at14381_at17387_s_at19577_at14384_at17413_s_at19593_at14487_at17416_at19602_at14597_at17425_s_at19618_at14705_i_at17440_i_at19670_at14709_at17473_at19696_at14779_at17533_s_at19722_s_at14947_at17549_s_at19749_at14950_at17654_at19755_at14998_at17693_at19815_at15045_at17697_at19926_at15109_s_at17755_at19968_at15124_s_at17832_s_at19977_at TABLE 272X ROOT SPECIFIC (COLD, SALINE& OSMOTIC STRESSES)11997_at14069_at16052_at18327_s_at12004_at14072_at16053_i_at18597_at12051_at14073_at16105_s_at18607_s_at12072_at14097_at16161_s_at18636_at12150_at14139_at16165_s_at18663_s_at12151_at14235_at16298_at18782_at12166_i_at14250_r_at16334_s_at18885_at12219_at14578_s_at16422_at18888_at12315_at14582_at16427_at18942_at12332_s_at14640_s_at16440_s_at18955_at12374_i_at14643_s_at16442_s_at19060_at12482_s_at14644_s_at16468_at19108_at12515_at14658_s_at16488_at19135_at12522_at14659_s_at16511_at19137_at12538_at14711_s_at16529_at19195_at12571_s_at14900_at16553_f_at19263_at12574_at14924_at16568_s_at19376_at12609_at14990_at16914_s_at19406_at12678_i_at15018_at16965_s_at19432_s_at12698_at15022_at16981_s_at19835_at12749_at15107_s_at16989_at19836_at12760_g_at15116_f_at17033_s_at19840_s_at12765_at15120_s_at17066_s_at19841_at12768_at15124_s_at17085_s_at19843_at12769_at15131_s_at17252_at19926_at12772_at15132_s_at17376_at19972_at12777_i_at15137_s_at17378_at19977_at12958_at15184_s_at17388_at19991_at12989_s_at15188_s_at17415_at20034_i_at13015_s_at15208_s_at17429_s_at20042_s_at13134_s_at15252_g_at17463_at20189_at13146_s_at15343_at17485_s_at20194_at13172_s_at15389_at17490_s_at20200_at13178_at15392_at17567_at20214_i_at13179_at15448_at17585_s_at20239_g_at13187_i_at15503_at17595_s_at20262_at13211_s_at15531_i_at17840_s_at20269_at13239_s_at15594_s_at17860_at20294_at13273_s_at15609_s_at17880_s_at20312_s_at13297_s_at15623_f_at17894_at20382_s_at13549_at15639_s_at17896_at20396_at13604_at15670_s_at17899_at20432_at13629_s_at15680_s_at17911_at20444_at13706_s_at15859_at17935_at20446_s_at13714_at15900_at17961_at20480_s_at13751_at15923_at18024_s_at20586_i_at13895_at15962_s_at18122_at20612_s_at13933_at15964_s_at18222_at20672_at13967_at15965_at18224_s_at20686_at13985_s_at15975_s_at18252_at20689_s_at14028_at15985_at18255_at14030_at16001_at18269_s_at14058_at16048_at18270_at TABLE 282X LEAF SPECIFIC (COLD, SALINE& OSMOTIC STRESSES)12169_i_at16136_s_at12186_at16172_s_at12187_at16316_at12211_at16385_s_at12212_at16455_at12214_g_at16485_s_at12270_at16512_s_at12645_at16547_s_at12754_g_at16548_s_at12774_at16629_s_at12793_at16673_at12796_s_at16899_at12910_s_at17010_s_at12916_s_at17018_s_at12953_at17054_s_at13090_at17095_s_at13124_at17097_s_at13335_at17273_at13550_at17394_s_at13567_at17420_at13568_at17449_s_at13596_at17600_s_at13614_at17843_s_at13678_s_at17913_s_at13719_at17966_at14014_at18003_at14096_at18081_at14118_i_at18560_at14369_at18588_at14478_at18626_at14513_s_at18644_at14540_at18666_s_at14596_at18742_f_at14733_s_at18977_at14986_at18994_at15045_at19227_at15097_s_at19373_at15098_s_at19834_at15145_s_at19867_at15153_s_at19998_at15154_s_at20062_at15182_s_at20199_at15203_s_at20256_s_at15372_at20284_at15521_s_at20437_at15581_s_at20442_i_at15621_f_at20450_at15642_s_at20468_at15776_at20547_at15910_at20635_s_at16017_at16046_s_at16115_s_at TABLE 292X TRANSCRIPTION (COLD, SALINE& OSMOTIC STRESSES)12068_at15665_s_at19836_at12166_i_at15679_s_at19860_at12374_i_at15720_at19866_at12392_at15871_s_at19898_at12431_at16072_s_at20262_at12450_s_at16073_f_at20335_s_at12503_at16105_s_at20362_at12536_s_at16111_f_at20424_at12540_s_at16127_s_at20437_at12541_at16534_s_at20456_at12587_at16582_s_at20515_s_at12594_at16589_s_at20635_s_at12595_at16747_at12704_f_at17019_s_at12705_f_at17129_s_at12709_f_at17160_at12712_f_at17520_s_at12719_f_at17538_s_at12724_f_at17555_s_at12725_r_at17609_at12726_f_at17896_at12734_f_at17971_s_at12736_f_at17975_at12737_f_at17978_s_at12812_at18121_s_at12949_at18167_s_at12951_at18197_at12966_s_at18222_at13023_at18318_at13034_s_at18576_s_at13087_at18629_s_at13270_at18738_f_at13273_s_at18742_f_at13432_at18744_f_at13555_at18745_f_at13688_s_at18747_f_at13714_at18750_f_at13965_s_at18751_f_at13987_s_at18789_at14003_at18834_at14144_at18942_at14178_at19083_at14223_at19202_at14235_at19209_s_at14303_s_at19232_s_at14393_at19315_at14553_at19489_s_at14781_at19611_s_at15046_s_at19646_s_at15053_s_at19707_s_at15214_s_at19722_s_at15510_r_at19744_at15638_s_at19755_at TABLE 302X PHOSPHATES (COLD, SALINE & OSMOTIC STRESSES)12470_at12556_at13128_at13135_s_at13180_s_at13192_s_at13193_s_at13587_at13995_at14335_at15073_at15171_s_at15240_at15586_s_at15641_s_at15651_f_at15990_at16232_s_at16576_f_at16753_at17423_s_at17525_s_at17537_s_at17929_s_at17954_s_at18012_s_at18308_i_at18616_at18847_at18936_at18980_at19243_at19263_at19638_at19883_at19932_at20333_at20393_at20570_at TABLE 312X KINASES (COLD, SALINE & OSMOTIC 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