Plant Molecular Biology

, Volume 37, Issue 3, pp 425–435 | Cite as

Regulation of abscisic acid-induced transcription

  • Peter K. Busk
  • Montserrat Pagès


The phytohormone abscisic acid is probably present in all higher plants. This hormone is necessary for regulation of several events during seed development and for the response to environmental stresses such as desiccation, salt and cold. An important part of the physiological response to abscisic acid is achieved through gene expression.

Here, we summarize the current knowledge of regulation of abscisic acid-induced transcription. The main focus is on a description of the known abscisic acid-responsive cis-elements, their properties and the possible transacting factors binding to the elements. Results have shown that cooperative action of cis-elements and the promoter configuraton is crucial for regulation by abscisic acid. Furthermore, several elements are organ- and species-specific. Recent studies of the chromatin structure of abscisic acid-responsive genes point to the importance of induction of transcription by coactivators or by phosphorylation/dephosphorylation of transcription factors. An interesting example of activation by a cofactor is the cooperative action between abscisic acid-signaling and the regulatory protein Viviparous 1 through the abscisic acid responsive element.

gene expression protein-DNA interaction plant stress seed development 


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  1. 1.
    Abe H, Yamaguchi-Shinozaki K, Urao T, Iwasaki T, Hosokawa D, Shinozaki K: Role of Arabidospis MYC and MYB homologs in droughtand abscisic acidregulated gene expression. Plant Cell 9: 1859–1868 (1997).PubMedGoogle Scholar
  2. 2.
    Baker SS, Wilhelm KS, Thomashow MF: The 5′region of Arabidopsis thaliana cor15A has cis-acting elements that confer cold, droughtand ABAregulated gene expression. Plant Mol Biol 24: 701–713 (1994).PubMedGoogle Scholar
  3. 3.
    Bartels D, Schneider K, Terstappen G, Piatkowski D, Salamini F: Molecular cloning of ABA-modulated genes from the resurrection plant Craterostigma plantagineum which are induced during desiccation. Planta 181: 27–34 (1990).CrossRefGoogle Scholar
  4. 4.
    Benfey PN, Ren L, Chua N-H: The CaMV 35S enhancer contains at least two domains which can confer different developmental and tissuespecific expression patterns. EMBO J 8: 2195–2202 (1989).Google Scholar
  5. 5.
    Bertauche N, Leung J, Giraudat J: Protein phosphatase activity of abscisic acid insensitive 1 (ABI1) protein from Arabidopsis thaliana. Eur J Biochem 241: 193–200 (1996).PubMedGoogle Scholar
  6. 6.
    Bohnert HJ, Nelson DE, Jensen RG: Adaptations to environmental stresses. Plant Cell 7: 1099–1111 (1995).CrossRefPubMedGoogle Scholar
  7. 7.
    Bray EA: Molecular responses to water deficit. Plant Physiol 103: 1035–1040 (1993).PubMedGoogle Scholar
  8. 8.
    Bray EA, Moses MS, Morabito D, Hong B, Shih T-Y, Imay R: Exogenous ABA does not mimic endogenous ABA in the induction of gene expression. In: Workshop on Abscisic Acid Signal Transduction in Plants. Instituto Juan March de Estudios e Investigaciones, Madrid, Spain (1996).Google Scholar
  9. 9.
    Busk PK, Pagès M: Protein binding to the abscisic acidresponsive element is independent of VIVIPAROUS1 in vivo. Plant Cell 9: 2261–2270 (1997).PubMedGoogle Scholar
  10. 10.
    Busk PK, Jensen AB, Pagès M: Regulatory elements in vivo in the promoter of the abscisic acid responsive gene rab17 from maize. Plant J 11: 1285–1295 (1997).PubMedGoogle Scholar
  11. 11.
    Chandler PM, Robertson M: Gene expression regulated by abscisic acid and its relation to stress tolerance. Annu Rev Plant Physiol. Plant Mol Biol 45: 113–141 (1994).Google Scholar
  12. 12.
    Close TJ: Dehydrins: Emergence of a biochemical role of a family of plant dehydration proteins. Physiol Plant 97: 795–803 (1996).Google Scholar
  13. 13.
    Cohen A, Bray EA: Characterization of three mRNAs that accumulate in wilted tomato leaves in response to elevated levels of endogenous abscisic acid. Planta 182: 27–33 (1990).CrossRefGoogle Scholar
  14. 14.
    Cohen A, Plant AP, Moses MS, Bray EA: Organspecific and environmentally regulated expression of two abscisic acidinduced genes of tomato. Plant Physiol 97: 1367–1374 (1991).Google Scholar
  15. 15.
    Davies WJ, Metcalfe JC, Lodge TA, da Costa AR: Hormones as chemical signals involved in root to shoot communication of effects of changes in the soil environment. In: Hoad, GV (ed) Hormone Action in Plant Development. A Critical Appraisal, pp. 201–216. Butterworths, London, UK (1987).Google Scholar
  16. 16.
    Dolferus R, Jacobs M, Peacock WJ, Dennis ES: Differential interactions of promoter elements in stress responses of the Arabidopsis Adh gene. Plant Physiol 105: 1075–1087 (1994).CrossRefPubMedGoogle Scholar
  17. 17.
    Donald RGK, Cashmore AR: Mutation of either G box or I box sequences profoundly affects expression of the Arabidopsis rbcS-1A promoter. EMBO J 9: 1717–1726 (1990).PubMedGoogle Scholar
  18. 18.
    Felsenfeld G: Chromatin as an essential part of the transcriptional mechanism. Nature 355: 219–224 (1992).PubMedGoogle Scholar
  19. 19.
    Finkelstein RR: Abscisic acidinsensitive mutations provide evidence for stage-specific signal pathways regulating expression of an Arabidopsis late embryogenesis-abundant (lea) gene. Mol Gen Genet 238: 401–408 (1993).CrossRefPubMedGoogle Scholar
  20. 20.
    Foster R, Izawa T, Chua N-H: Plant bZIP proteins gather at ACGT elements. FASEB J 8: 192–200 (1994).PubMedGoogle Scholar
  21. 21.
    Furini A, Koncz C, Salamini F, Bartels D: High level transcription of a member of a repeated gene family confers dehydration tolerance to callus tissue of Craterostigma Plantagineum. EMBO J 16: 3599–3608 (1997).PubMedGoogle Scholar
  22. 22.
    Galau GA, Bijaisoradat N, Hughes DW: Accumulation kinetics of cotton late embryogenesis-abundant mRNAs and storage protein mRNAs coordinate regulation during embryogenesis and the role of abscisic acid. Dev Biol 123: 198–212 (1987).PubMedGoogle Scholar
  23. 23.
    Galau GA, Jakobsen KS, Hughes DW: The controls of late dicot embryogenesis and early germination. Physiol Plant 81: 280–288 (1991).CrossRefGoogle Scholar
  24. 24.
    García-Garrido JM, Fanlo J, Delseny M, Martínez-Izquierdo JA: The ABRElike or couplinglike ACGCGTGG element of rice Ltp2 promoter is necessary for ABA response. In: Workshop on Abscisic Acid Signal Transduction in Plants. Instituto Juan March de Estudios e Investigaciones. Madrid. Spain (1996).Google Scholar
  25. 25.
    Gilmour SJ, Thomashow MF: Cold acclimation and coldregulated gene expression in ABA mutants of Arabidopsis thaliana. Plant Mol Biol 17: 1233–1240 (1991).PubMedGoogle Scholar
  26. 26.
    Giraudat J, Hauge BM, Valon C, Smalle J, Parcy F, Goodman HM: Isolation of the Arabidopsis ABI3 gene by positional cloning. Plant Cell 4: 1251–1261 (1992).CrossRefPubMedGoogle Scholar
  27. 27.
    Giraudat J, Parcy F, Bertauche N, Gosti F, Leung J, Morris PC, Bouvier-Durand M, Vartanian N: Current advances in abscisic acid action and signalling. Plant Mol Biol 26: 1557–1577 (1994).PubMedGoogle Scholar
  28. 28.
    Gomez J, Sanchez-Martinez D, Steifel V, Rigau J, Puigdomenech P, Pagès M: A gene induced by the plant hormone abscisic acid in response towater stress encodes a glycinerich protein. Nature 334: 262–264 (1988).CrossRefPubMedGoogle Scholar
  29. 29.
    Guiliano G, Pichersky E, Malik VS, Timko MP, Scolnik P, Cashmore AR: An evolutionarily conserved protein binding sequence upstream of a plant lightregulated gene. Proc Natl Acad Sci USA 85: 7089–7093 (1988).PubMedGoogle Scholar
  30. 30.
    Guiltinan MJ, Marcotte WR, Quatrano RS: A plant leucine zipper protein that recognizes an abscisic acid response element. Science 250: 267-271 (1990).PubMedGoogle Scholar
  31. 31.
    Hattori T, Vasil V, Rosenkras L, Hannah LC, McCarty DR, Vasil IK: The viviparous-1 gene and abscisic acid activa te the C1 regulatory gene for anthocyanin biosynthesis during seed maturation in maize. Genes Dev 6: 609–618 (1992).PubMedGoogle Scholar
  32. 32.
    Hattori T, Terada T, Hamasuna S: Regulation of the Osem gene by abscisic acid and the transcriptional activator VP1: analysis of cis-acting promoter elements required for regulation by abscisic acid and VP1. Plant J 7: 913–925 (1995).CrossRefPubMedGoogle Scholar
  33. 33.
    Heimovaara-Dijkstra S, Nieland TJF, van der Meulen RM, Wang M: Abscisic acid-induced gene expression requires the activity of protein(s) sensitive to the protein-tyrosine phosphatase inhibitor phenylarsine oxide. Plant Growth Regul 18: 115–123 (1996).Google Scholar
  34. 34.
    Hildmann T, Ebneth M, PeZa-CortJs H, Sanchez-Serrano JJ, Willmitzer L, Prat S: General roles of abscisic and jasmonic acids in gene activation as a result of mechanical wounding. Plant Cell 4: 1157–1170 (1992).CrossRefPubMedGoogle Scholar
  35. 35.
    Hill A, Nantel A, Rock CD, Quatrano RS: A conserved domain of the viviparous-1 gene product enhances the DNA binding activity of the bZIP protein EmBP1 and other transcription factors. J Biol Chem 271: 3366–3374 (1996).CrossRefPubMedGoogle Scholar
  36. 36.
    Hughes DW, Galau GA: Temporally modular gene expression during cotyledon development. Genes Dev 3: 358–369 (1989).PubMedGoogle Scholar
  37. 37.
    Hughes DW, Galau GA: Developmental and environmental induction of Lea and LeaA mRNAs and the postabscission program duringembryo culture. PlantCell 3: 605–618 (1991).Google Scholar
  38. 38.
    Hunter T: Protein kinases and phosphatases: the Yin andYang of protein phosphorylation and signaling. Cell 80: 225–236 (1995).CrossRefPubMedGoogle Scholar
  39. 39.
    Imay R, Moses MS, Bray EA: Expression of an ABAinduced gene of tomato in transgenic tobacco during periods of water deficit. J Exp Bot 46: 1077–1084 (1995).Google Scholar
  40. 40.
    Iturriaga G, Leyns L, Villegas A, Gharaibeh R, Salamini F, Bartels D: A family of novel myb-related genes from the resurrection plant Craterostigma Plantagineum are specifically expressed in callus and roots in response to ABA or desiccation. Plant Mol Biol 32: 707–716 (1996).PubMedGoogle Scholar
  41. 41.
    Iwasaki T, Yamaguchi-Shinozaki K, Shinozaki K: Identification of a cis-regulatory region of a gene in Arabidopsis thaliana whose induction by dehydration is mediated by abscisic acid and requires protein synthesis. Mol Gen Genet 247: 391–398 (1995).CrossRefPubMedGoogle Scholar
  42. 42.
    Izawa T, Foster R, Chua N-H: Plant bZIP protein DNA binding specificity. J Mol Biol 230: 1131–1144 (1993).CrossRefPubMedGoogle Scholar
  43. 43.
    Jensen AB, Busk PK, Figueras M, Mar Albà M, Peracchia G, Messeguer R, Goday A, Pagès M: Drought signal transduction in plants. Plant Growth Regulation 20: 105–110 (1996).Google Scholar
  44. 44.
    Jiang C, Iu B, Singh J: Requirement of a CCGAC cisacting element for cold induction of the BNII5 gene from winter Brassica napus. Plant Mol Biol 30: 679–684 (1996).PubMedGoogle Scholar
  45. 45.
    Kao C-Y, Cocciolone SM, Vasil IK, McCarty DR: Localization and interaction of the cis-acting elements for abscisic acid, VIVIPAROUS1, and light activation of the C1 gene of maize. Plant Cell 8: 1171–1179 (1996).PubMedGoogle Scholar
  46. 46.
    Kim SY, Chung HJ, Thomas TL: Isolation of a novel class of bZIP transcription factors that interact with ABAresponsive and embryospecification elements in the Dc3 promoter using a modified yeast onehybrid system. Plant J 11: 1237–1251 (1997).PubMedGoogle Scholar
  47. 47.
    King RW: Abscisic acid in developing wheat grains and its relationship to grain growth and maturation. Planta 132: 43–61 (1976).Google Scholar
  48. 48.
    Knetsch MLW, Wang M, Snaar-Jagalska BE, Heimovaara-Dijkstra S: Abscisic acid induces mitogenactivated protein kinase activation in barley aleurone protoplasts. Plant Cell 8: 1061–1067 (1996).CrossRefPubMedGoogle Scholar
  49. 49.
    Koornneef M: Genetic aspects of abscisic acid. In: Blonstein AD, King PJ (eds) A Genetic Approach to Plant Biochemistry, pp. 35–54. Springer Verlag, Vienna, Austria (1986).Google Scholar
  50. 50.
    Koornneef M, Hanhart CJ, Hilhorst HWM, Karssen CM: In vivo inhibition of seed development and reserve protein accumulation in recombinants of abscisic acid biosynthesis and responsiveness mutants in Arabidopsis thaliana. Plant Physiol 90: 463–469 (1989).Google Scholar
  51. 51.
    Lam E, Chua N-H: Tetramer of a 21base pair synthetic element confers seed expression and transcriptional enhancement in response to water stress and abscisic acid. J Biol Chem 266: 17131–17135 (1991).PubMedGoogle Scholar
  52. 52.
    Leung J, Giraudat J: Abscisic acid signal transduction. Ann. Rev. Plant Physiol Plant Mol Biol, in press (1998).Google Scholar
  53. 53.
    Leung J, Merlot S, Giraudat J: The Arabidopsis ABSCISIC ACIDINSENSITIVE (ABI2) and ABI1 genes encode homologous protein phosphatases 2C involved in abscisic acid signal transduction. Plant Cell 9: 759–771 (1997).CrossRefPubMedGoogle Scholar
  54. 54.
    Loake GJ, Faktor O, Lamb CJ, Dixon RA: Combination of Hbox (CCTACCN7CT) and Gbox (CACGTG) cis elements is necessary for feed-forward stimulation of a chalcone synthase promoter by the phenylpropanoidpathway intermediate pcoumaric acid. Proc Natl Acad Sci USA 89: 9230–2934 (1992).Google Scholar
  55. 55.
    Lu G, Paul AL, McCarty DR, Ferl RJ: Transcription Factor Veracity: is GBF3 responsible for ABAregulated expression of Arabidopsis Adh? Plant Cell 8: 847–857 (1996).PubMedGoogle Scholar
  56. 56.
    Marcotte WD Jr, Russell SH, Quatrano RS: Abscisic acidresponsive sequences from the Em gene of wheat. Plant Cell 1: 969–976 (1989).CrossRefPubMedGoogle Scholar
  57. 57.
    McCarty DR: Genetic control and integration of maturation and germination pathways in seed development. Annu Rev Plant Physiol Plant Mol Biol 46: 71–93 (1995).CrossRefGoogle Scholar
  58. 58.
    McCarty DR, Hattori T, Carson CB, Vasil V, Lazar M, Vasil IK: The Viviparous1 developmental gene of maize encodes a novel trancriptional activator. Cell 66: 895–905 (1991).CrossRefPubMedGoogle Scholar
  59. 59.
    McKendree WL Jr, Paul AL, DeLisle AJ, Ferl RJ: In vivo and in vitro characterization of protein interactions with the dyad Gbox of the Arabidopsis Adh gene. Plant Cell 2: 207–214 (1990).CrossRefPubMedGoogle Scholar
  60. 60.
    McKendree WL, Jr, Ferl RJ: Functional elements of the Arabidopsis Adh promoter include the Gbox. Plant Mol Biol 19: 859–862 (1992).PubMedGoogle Scholar
  61. 61.
    Mundy J, Chua N-H: Abscisic acid and waterstress induce the expression of a novel rice gene. EMBO J 7: 2279–2286 (1988).PubMedGoogle Scholar
  62. 62.
    Mundy J, Yamaguchi-Shinozaki K, Chua N-H: Nuclear proteins bind conserved elements in the abscisic acid-responsive promoter of a rice RAB gene. Proc Natl Acad Sci USA 87: 1406–1410 (1990).PubMedGoogle Scholar
  63. 63.
    Nakagawa H, Ohmiya K, Hattori T: A rice bZIP protein, designated OSBZ8, is rapidly induced by abscisic acid. Plant J 9: 217–227 (1996).PubMedGoogle Scholar
  64. 64.
    Neill SJ, Horgan R, Parry AD: The carotenoid and abscisic acid content of viviparous kernels and seedlings of Zea mays L. Planta 169: 87–96 (1986).Google Scholar
  65. 65.
    Neill SJ, Horgan R, Rees AF: Seed development and vivipary in Zea mays L. Planta 171: 358–364 (1987).Google Scholar
  66. 66.
    Nelson D, Salamini F, Bartels D: Abscisic acid promotes novel DNA-binding activity to a desiccation-related promoter of Craterostigma Plantagineum. Plant J 5: 451–458 (1994).CrossRefPubMedGoogle Scholar
  67. 67.
    Niogret MF, Culiañez-Macià FA, Goday A, Albà MM, Pagès M: Expression and cellular localization of rab28 mRNA and Rab28 protein during maize embryogenesis. Plant J 9: 549–557 (1996).PubMedGoogle Scholar
  68. 68.
    Niu X, Adams CC, Workman JL, Guiltinan MJ: Binding of the wheat basic leucine zipper protein EmBP-1 to nucleosomal binding sites is modulated by nucleosome positioning. Plant Cell 8: 1569–1587 (1996).PubMedGoogle Scholar
  69. 69.
    Nordin K, Heino P, Palva ET: Separate signal pathways regulate the expression of a low-temperatureinduced gene in Arabidopsis thaliana (L.) Heynh. Plant Mol Biol 16: 1061–1071 (1991).PubMedGoogle Scholar
  70. 70.
    Ono A, Izawa T, Chua N-H, Shimamoto K: The rab16B promoter of rice contains two distinct abscisic acidresponsive elements. Plant Physiol 112: 483–491 (1996).PubMedGoogle Scholar
  71. 71.
    Parcy F, Giraudat J: Interactions between the ABI1 and the ectopically expressed ABI3 genes in controlling abscisic acid responses in Arabidopsis vegetative tissues. Plant J 11: 693–702 (1997).PubMedGoogle Scholar
  72. 72.
    Parcy F, Valon C, Raynal M, Gaubier-Comella P, Delseny M, Giraudat J: Regulation of gene expression programs during Arabidopsis seed development: Roles of the ABI3 locus and of endogenous abscisic acid. Plant Cell 6: 1567–1582 (1994).CrossRefPubMedGoogle Scholar
  73. 73.
    Peña-Cortès H, Sanchez-Serrano JJ, Mertens R, Willmitzer L, Prat S: Abscisic acid is involved in the woundinduced expression of the proteinase inhibitor II gene in potato and tomato. Proc Natl Acad Sci USA 86: 9851–9855 (1989).Google Scholar
  74. 74.
    Peña-Cortès H, Willmitzer L, Sanchez-Serrano JJ: Abscisic acid mediates the wound induction but not developmentalspecific expression of the proteinase inhibitor II gene family. Plant Cell 3: 963–972 (1991).CrossRefPubMedGoogle Scholar
  75. 75.
    Phillips J, Artsaenko O, Fiedler U, Horstmann C, Mock HP, Muntz K, Conrad U: Seed-specific immunomodulation of abscisic acid activity induces a developmental switch. EMBO J 16: 4489–4496 (1997).PubMedGoogle Scholar
  76. 76.
    Pla M, Goday A, Vilardell J, Gomez J, Pagès M: Differential regulation of ABAinduced 23–25 kDA proteins in embryo and vegetative tissues of the viviparous mutants of maize. Plant Mol Biol 13: 385–394 (1989).PubMedGoogle Scholar
  77. 77.
    Pla M, Gomez J, Goday A, Pagès M: Regulation of the abscisic acidresponsive gene rab28 in maize viviparous mutants. Mol Gen Genet 230: 394–400 (1991).CrossRefPubMedGoogle Scholar
  78. 78.
    Plant AL, Cohen A, Moses MS, Bray EA: Nucleotide sequence and spatial expression pattern of a drought-and ABA-induced gene of tomato. Plant Physiol 97: 900–906 (1991).Google Scholar
  79. 79.
    Puente P, Wei N, Deng XW: Combinatorial interplay of promoter elements constitutes the minimal determinants for light and developmental control of gene expression in Arabidopsis. EMBO J 15: 3732–3743 (1996).PubMedGoogle Scholar
  80. 80.
    Robertson AJ, Ishikawa M, Gusta LV, MacKenzie SL: Abscisic acidinduced heat tolerance in Bromus inermis Leyss cellsuspension cultures. Heatstable, abscisic acidresponsive polypeptides in combination with sucrose confer anhanced thermostability. Plant Physiol 105: 181–190 (1994).PubMedGoogle Scholar
  81. 81.
    Robichaud CS, Wong J, Sussex IM: Control of in vitro growth of viviparous embryo mutants of maize by abscisic acid. Dev Genet 1: 325–330 (1980).Google Scholar
  82. 82.
    Rogers JC, Rogers SW: Definition and functional implications of gibberellin and abscisic acid cis-acting hormone response complexes. Plant Cell 4: 1443–1451 (1992).CrossRefPubMedGoogle Scholar
  83. 83.
    Salinas J, Oeda K, Chua N-H: Two GBoxrelated sequences confer different expression patterns in transgenic tobacco. Plant Cell 4: 1485–1493 (1992).Google Scholar
  84. 84.
    Schultz TF, Spiker S, Quatrano RS: Histone H1 enhances the DNA binding activity of the transcription factor EmBP-1. J Biol Chem 271: 25742–25745 (1996).PubMedGoogle Scholar
  85. 85.
    Sheen J: Ca2+-dependent protein kinases and stress signal transduction in plants. Science 274: 1900–1902 (1996).PubMedGoogle Scholar
  86. 86.
    Shen Q, Ho T-HD: Functional dissection of an abscisic acid (ABA)inducible gene reveals two independent ABAresponsive complexes each containing a G-box and a novel cis-acting element. Plant Cell 7: 295–307 (1995).CrossRefPubMedGoogle Scholar
  87. 87.
    Shen Q, Zhang P, Ho T-HD: Modular nature of abscisic acid (ABA) response complexes: Composite promoter units that are necessary and sufficient for ABA induction of gene expression in barley. Plant Cell 8: 1107–1119 (1996).PubMedGoogle Scholar
  88. 88.
    Shinozaki K, Yamaguchi-Shinozaki K: Molecular responses to drought and cold stress. Curr Opin Biotechnol 7: 161–167 (1996).PubMedGoogle Scholar
  89. 89.
    Skriver K, Mundy J: Gene expression in response to abscisic acid and osmotic stress. Plant Cell 2: 503–512 (1990).CrossRefPubMedGoogle Scholar
  90. 90.
    Skriver K, Olsen FL, Rogers JC, Mundy J: cisacting elements responsive to gibberellin and its antagonist abscisic acid. Proc Natl Acad Sci USA 88: 7266–7270 (1991).PubMedGoogle Scholar
  91. 91.
    Stockinger EJ, Gilmour SJ, Thomashow MF: Arabidopsis thaliana CBF1 encodes an AP2 domain-containing transcriptional activator that binds to the C-repeat/ DRE, a cisacting DNA regulatory element that stimulates transcription in response to low temperature and water deficit. Proc Natl Acad Sci USA 94: 1035–1040 (1997).PubMedGoogle Scholar
  92. 92.
    Straub PF, Shen Q, Ho T-HD: Structure and promoter analysis of an ABA and stress regulated barley gene, HVA1. Plant Mol Biol 26: 617–630 (1994).PubMedGoogle Scholar
  93. 93.
    Suzuki M, Kao CY, McCarty DR: The conserved B3 domain of VIVIPAROUS1 has a cooperative DNA binding activity. Plant Cell 9: 799–807 (1997).PubMedGoogle Scholar
  94. 94.
    Suzuki Y, Kurogochi S, Nurofushi N, Ota Y, Takahashi N: Seasonal changes in GA1, GA19 and abscisic acid in three rice cultivars. Plant Cell Physiol 22: 1085–1093 (1981).Google Scholar
  95. 95.
    Svaren J, Hörz W: Transcription factor vs nucleosomes: regulation of the PHO5 promoter in yeast. TIBS 22: 93–97 (1997).PubMedGoogle Scholar
  96. 96.
    Taylor JE, Renwick KF, Webb AAR, McAinsh MR, Furini A, Bartels D, Quatrano RS, Marcotte WR Jr, Hetherington AM:ABAregulated promoter activity in stomatal guard cells. Plant J 7: 129–134 (1995).CrossRefPubMedGoogle Scholar
  97. 97.
    Tjian R, Maniatis T: Transcriptional activation: A complex puzzle with few easy pieces. Cell 77: 5–8 (1994).CrossRefPubMedGoogle Scholar
  98. 98.
    Travers AA: DNA-Protein Interactions. Chapman and Hall, London, UK (1993).Google Scholar
  99. 99.
    Urao T, Yamaguchi-Shinozaki K, Urao S, Shinozaki K: An Arabidopsis myb homolog is induced by dehydration stress and its gene product binds to the conserved MYB recognition sequence. Plant Cell 5: 1529–1539 (1993).CrossRefPubMedGoogle Scholar
  100. 100.
    Urao T, Katagiri T, Mizoguchi T, Yamaguchi-Shinozaki K, Shinozaki K: Two genes that encode Ca2+dependent protein kinases are induced by drought and highsalt stresses in Arabidopsis thaliana. Mol Gen Genet 244: 331–340 (1994).CrossRefPubMedGoogle Scholar
  101. 101.
    Vasil V, Marcotte WR Jr, Rosenkrans L, Cocciolone SM, Vasil IK, Quatrano RS, McCarty R: Overlap of Viviparous1 (VP1) and abscisic acid response elements in the Em promoter: G-box elements are sufficient but not necessary for VP1 transactivation. Plant Cell 7: 1511–1518 (1995).CrossRefPubMedGoogle Scholar
  102. 102.
    Vega-Palas MA, Ferl RJ: The Arabidopsis Adh gene exhibits diverse nucleosome arrangements within a small DNase Isensitive domain. Plant Cell 7: 1923–1932 (1995).PubMedGoogle Scholar
  103. 103.
    de Vetten NC, Lu G, Ferl RJ: A maize protein associated with the G-box binding complex has homology to brain regulatory proteins. Plant Cell 4: 1295–1307 (1992).PubMedGoogle Scholar
  104. 104.
    Vilardell J, Goday A, Freire MA, Torrent M, Martinez C, Tornè JM, Pagès M: Gene sequence, developmental expression, and protein phosphorylation of RAB-17 in maize. Plant Mol Biol 14: 423–432 (1990).PubMedGoogle Scholar
  105. 105.
    Vilardell J, Martínez-Zapater JM, Goday A, Arenas C, Pagès M: Regulation of the rab17 gene promoter in transgenic Arabidopsis wildtype, ABA-deficient, and ABA-insensitive mutants. Plant Mol Biol 24: 561–569 (1994).PubMedGoogle Scholar
  106. 106.
    Wang M, Oppedijk BJ, Lu X, van Duijn B, Schilperoort RA: Apoptosis in barley aleurone during germination and its inhibition by abscisic acid. Plant Mol Biol 32: 1125–1134 (1996).PubMedGoogle Scholar
  107. 107.
    Ward JM, Pei Z-M, Schroeder JI: Roles of ion channels in initiation of signal transduction in higher plants. Plant Cell 7: 833–844 (1995).PubMedGoogle Scholar
  108. 108.
    Weisshaar B, Armstrong GA, Block A, Da Costa e Silva O, Hahlbrock K: Lightin-ducible and constitutively expressed DNA-binding proteins recognizing a plant promoter element with functional relevance in light responsiveness. EMBO J 10: 1777–1786 (1991).PubMedGoogle Scholar
  109. 109.
    Williamson JD, Scandalios JG: Differential response ofmaize catalases to abscisic acid: Vp1 transcriptional activator is not required for abscisic acidregulated Cat1 expression. Proc Natl Acad Sci USA 89: 8842–8846 (1992).Google Scholar
  110. 110.
    Wu Y, Kuzma J, Maréchal E, Graeff R, Lee HC, Foster R, Chua NH: Abscisic acid signaling through cyclic ADPribose in plants. Science 278: 2126–2130 (1997).PubMedGoogle Scholar
  111. 111.
    Yamaguchi-Shinozaki K, Mundy J, Chua N-H: Four tightly linked rab genes are differentially expressed in rice. Plant Mol Biol 14: 29–39 (1989).CrossRefGoogle Scholar
  112. 112.
    Yamaguchi-Shinozaki K, Shinozaki K: Characterization of the expression of a desiccationresponsive rd29 gene of Arabidopsis thaliana and analysis of its promoter in transgenic plants. Mol Gen Genet 236: 331–340 (1993).CrossRefPubMedGoogle Scholar
  113. 113.
    Yamaguchi-Shinozaki K, Shinozaki K: A novel cisacting element in an Arabidopsis gene is involved in responsivenes to drought, lowtemperature, or high-salt stress. Plant Cell 6: 251–264 (1994).CrossRefPubMedGoogle Scholar
  114. 114.
    Zeevaart JAD, Creelman RA: Metabolism and physiology of abscisic acid. Annu Rev Plant Physiol Plant Mol Biol 39: 439–473 (1988).CrossRefGoogle Scholar

Copyright information

© Kluwer Academic Publishers 1998

Authors and Affiliations

  • Peter K. Busk
    • 2
  • Montserrat Pagès
    • 1
  1. 1.Departament de Genética Molecular. Centre d'Investigació i Desenvolupament. C.S.I.CBarcelonaSpain
  2. 2.Plantebiokemisk Laboratorium. Den kongelige Veterinær- og LandbohøjskoleFrederiksberg CDenmark

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