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The 5′-region of Arabidopsis thaliana cor15a has cis-acting elements that confer cold-, drought- and ABA-regulated gene expression

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Abstract

Previous nuclear run-on experiments indicated that the cor15a (cold-regulated) gene of Arabidopsis thaliana L. (Heyn) has a cold-inducible promoter (Hajela et al., Plant Physiol 93: 1246–1252, 1990). The data presented here indicate that the 5′ region of cor15a between nucleotides −305 and +78 (relative to the start of transcription) contains a cis-acting element(s) that can impart cold-regulated gene expression. Histochemical staining experiments indicated that the cor15a promoter is inactive, or very weakly active, in most of the tissues and organs of plants grown at normal temperature and that it becomes activated throughout most of the plant in response to low temperature. Notable exceptions to this general pattern include constitutive activity of the promoter in anthers of control grown plants and apparent inactivity of the promoter in the roots and ovaries of cold-treated plants. Histochemical staining experiments also indicated that low temperature regulation of cor15a does not involve the synthesis of a regulatory molecule that can spread throughout the plant and induce cor gene expression at normal growth temperature. Finally, gene fusion experiments indicated that the 5′ region of cor15a between nucleotides −305 and +78, in addition to imparting cold-regulated gene expression, can impart ABA- and drought-regulated gene expression.

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References

  1. An G, Ebert PR, Mitra A, Ha SB: Binary vectors. In: Gelvin SB, Schilperoort RA (eds) Plant Molecular Biology Manual, pp. A3: 1–19. Kluwer Academic Publishers, Dordrecht (1988).

    Google Scholar 

  2. De Block M, Debrouwer D: In-situ enzyme histochemistry on plastic-embedded plant material. The development of an artefact-free β-glucuronidase assay. Plant J 2: 261–266 (1992).

    Google Scholar 

  3. Gilmour SJ, Artus NN, Thomashow MF: cDNA sequence analysis and expression of two cold-regulated genes of Arabidopsis thaliana. Plant Mol Biol 18: 13–21 (1992).

    Google Scholar 

  4. Gilmour SJ, Hajela RK, Thomashow MF: Cold acclimation in Arabidopsis thaliana. Plant Physiol 87: 745–750 (1988).

    Google Scholar 

  5. Gilmour SJ, Thomashow MF: Cold acclimation and cold-regulated gene expression in ABA mutants of Arabidopsis thaliana. Plant Mol Biol 17: 1233–1240 (1991).

    Google Scholar 

  6. Guiltinan MJ, Marcotte WR, Quatrano RS: A plant leucine zipper protein that recognizes an abscisic acid response element. Science 250: 267–271 (1990).

    Google Scholar 

  7. Guy CL: Cold acclimation and freezing stress tolerance: role of protein metabolism. Annu Rev Plant Physiol Plant Mol Biol 41: 187–223 (1990).

    Google Scholar 

  8. Hajela RK, Horvath DP, Gilmour SJ, Thomashow MF: Molecular cloning and expression of cor (cold-regulated) genes in Arabidopsis thaliana. Plant Physiol 93: 1246–1252 (1990).

    Google Scholar 

  9. Hoekema A, Hirsch PR, Hooykaas PJJ, Schilperoort RA. A binary plant vector strategy based on separation of vir- and T-region of the Agrobacterium tumefaciens Tiplasmid. Nature 303: 179–180 (1983).

    Google Scholar 

  10. Horvath DP, McLarney BK, Thomashow MF: Regulation of Arabidopsis thaliana L. (Heyn) cor78 in response to low temperature. Plant Physiol 103: 1047–1053 (1993).

    Google Scholar 

  11. Jefferson RA: Assaying chimeric genes in plants: The GUS gene fusion system. Plant Mol Biol Rep 5: 387–405 (1987).

    Google Scholar 

  12. Joshi CP: An inspection of the domain between putative TATA box and translation start site in 79 plant genes. Nucl Acids Res 15: 6643–6653 (1987).

    Google Scholar 

  13. Koornneef M, Reuling G, Karssen CM: The isolation and characterization of abscisic acid-insensitive mutants of Arabidopsis thaliana. Physiol Plant 61: 377–383 (1984).

    Google Scholar 

  14. Kurkela S, Borg-Franck M: Structure and expression of kin2, one of two cold- and ABA-induced genes of Arabidopsis thaliana. Plant Mol Biol 19: 689–692 (1992).

    Google Scholar 

  15. Kurkela S, Franck M: Cloning and characterization of a cold- and ABA-inducible Arabidopsis gene. Plant Mol Biol 15: 137–144 (1990).

    Google Scholar 

  16. Lång V, Palva ET: The expression of a rab-related gene, rab18, is induced by abscisic acid during the cold acclimation process of Arabidopsis thaliana (L.). Heynh. Plant Mol Biol 20: 951–962 (1992).

    Google Scholar 

  17. Lin C: A Molecular genetic study of cold acclimation in Arabidopsis thaliana. Doctoral dissertation, Michigan State University, East Lansing, MI (1992).

  18. Lin C, Thomashow MF: DNA sequence analysis of a complementary DNA for cold-regulated Arabidopsis gene cor15 and characterization of the COR15 polypeptide. Plant Physiol 99: 519–525 (1992).

    Google Scholar 

  19. Lin C, Thomashow MF: A cold-regulated Arabidopsis gene encodes a polypeptide having potent cryoprotective activity. Biochem Biophys Res Commun 183: 1103–1108 (1992).

    Google Scholar 

  20. Morgen BD, MacDonald MH, Leggewie G, Hurt AG: Several distinct types of sequence elements are required for efficient mRNA 3′ end formation in a pea rbcS gene. Mol Cell Biol 12: 5406–5414 (1992).

    Google Scholar 

  21. Mundy J, Yamaguchi-Shinozaki K, Chua N-H: Nuclear proteins bind conserved elements in the abscisic acidresponsive promoter of a rice rab gene. Proc Natl Acad Sci USA 87: 1406–1410 (1990).

    Google Scholar 

  22. Nordin K, Heino P, Palva ET: Separate signal pathways regulate the expression of a low-temperature-induced gene in Arabidopsis thaliana (L.) Heynh. Plant Mol Biol 16: 1061–1071 (1991).

    Google Scholar 

  23. Nordin K, Vahala T, Palva ET: Differential expression of two related, low-temperature-induced genes in Arabidopsis thaliana (L.) Heynh. Plant Mol Biol 21: 641–653 (1993).

    Google Scholar 

  24. Pla M, Vilardell J, Guiltinan MJ, Marcotte WR, Niogret MF, Quantrano RS, Pagès M: The cis-regulatory element CCACGTGG is involved in ABA and water-stress responses of the maize gene rab28. Plant Mol Biol 21: 259–266 (1993).

    Google Scholar 

  25. Rogers SO, Bendich AJ: Extraction of DNA from plant tissues. In: Gelvin SB, Schilperoort RA (eds) Plant Molecular Biology Manual, pp. A6: 1–10. Kluwer Academic Publishers, Dordrecht (1988).

    Google Scholar 

  26. Sambrook J, Fritsch EF, Maniatis T: Molecular Cloning. A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory, Cold Spring Harbor, NY (1989).

    Google Scholar 

  27. Sanger F, Nicklen S, Coulson AR: DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci USA 74: 5463–5467 (1977).

    Google Scholar 

  28. Schindler U, Menkens AE, Beckmann H, Ecker JR, Cashmore AR: Heterodimerization between light-regulated and ubiquitously expressed Arabidopsis GBF bZIP proteins. EMBO J 11: 1261–1273 (1992).

    Google Scholar 

  29. Steponkus PL, Webb MS: Freeze-induced dehydration and membrane destabilization in plants. In: Somero GN, Osmond CB and Bolis CL (eds) Water and Life: Comparative Analysis of Water Relationships at the Organismic, Cellular and Molecular Level, pp. 338–362. Springer-Verlag, Berlin (1992).

    Google Scholar 

  30. Takahashi T, Naito S, Komeda Y: The Arabidopsis HSP18.2 promoter/GUS gene fusion in transgenic Arabidopsis plants: a powerful tool for the isolation of regulatory mutants of the heat-shock response. Plant J 2: 751–761 (1992).

    Google Scholar 

  31. Thomashow MF: Molecular genetics of cold acclimation in higher plants. Ady Genet 28: 99–131 (1990).

    Google Scholar 

  32. Thomashow MF: Genes induced during cold acclimation in higher plants. In: Steponkus PL (ed) Advances in Low-Temperature Biology, vol. 2, pp. 183–210. JAI Press, London (1993).

    Google Scholar 

  33. Valvekens D, Van Montagu M, Van Lijsebettens M: Agrobacterium tumefaciens-mediated transformation of Arabidopsis thaliana root explants by using kanamycin selection. Proc Natl Acad Sci USA 85: 5536–5540 (1988).

    Google Scholar 

  34. Weiser CJ: Cold resistance and injury in woody plants. Science 169: 1269–1278 (1970).

    Google Scholar 

  35. Wilhelm KS, Thomashow MF: Arabidopsis thaliana cor15b, an apparent homolog of cor15a, is strongly responsive to cold and ABA, but not drought. Plant Mol Biol 123: 1073–1077 (1993).

    Google Scholar 

  36. Williams ME, Foster R, Chua NH: Sequences flanking the hexameric G-box core CACGTG affect the specificity of protein binding. Plant Cell 4: 485–496 (1992).

    Google Scholar 

  37. Yamaguchi-Shinozaki K, Shinozaki K: Characterization of the expression of a desiccation-responsive rd29 gene of Arabidopsis thaliana and analysis of its promoter in transgenic plants. Mol Gen Genet 236: 331–340 (1993).

    Google Scholar 

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Baker, S.S., Wilhelm, K.S. & Thomashow, M.F. The 5′-region of Arabidopsis thaliana cor15a has cis-acting elements that confer cold-, drought- and ABA-regulated gene expression. Plant Mol Biol 24, 701–713 (1994). https://doi.org/10.1007/BF00029852

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