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Abstract

Water availability and drought limit crop yields worldwide. The responses of plants to drought vary greatly depending on species and stress severity. These responses include changes in plant growth, accumulation of solutes, changes in carbon and nitrogen metabolism, and alterations in gene expression. In this article, we review cellular and molecular responses to water deficit, and their influence on plant dehydration tolerance.

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References

  1. Bartels D, Alexander R, Schneider K, Elster R, Velasco R, Alamillo J, Bianchi G, Nelson D and Salamini F (1993) Desiccation-related gene products analyzed in a resurrection plant and in barley embryos. In: Close TJ and Bray EA (eds) Plant Responses to Cellular Dehydration During Environmental Stress. Amer Soc Plant Physiol, pp 119–127

    Google Scholar 

  2. Blackman SA, Obendorf RL and Leopold AC (1992) Maturation proteins and sugars in desiccation tolerance of developing soybean seeds. Plant Physiol 100: 225–230

    Article  PubMed  CAS  Google Scholar 

  3. Boyer JS (1982) Plant productivity and environment. Science 218: 444–448

    Article  Google Scholar 

  4. Bray EA, Moses MS, Imai R, Cohen A and Plant AL (1993) Regulation of gene expression by endogenous abscisic acid during drought stress. In: Close TJ and Bray EA (eds) Plant Responses to Cellular Dehydration During Environmental Stress. Amer Soc Plant Physiol, pp 167–176

    Google Scholar 

  5. Chandler PM, Munns R and Robertson M (1993) Regulation of dehydrin expression. In: Close TJ and Bray EA (eds) Plant Responses to Cellular Dehydration During Environmental Stress. Amer Soc Plant Physiol, pp 159–166

    Google Scholar 

  6. Chrispeels MJ and Maurel C (1994) Aquaporins: the molecular basis of facilitated water movement through living plant cells? Plant Physiol 105: 9–13

    Article  PubMed  CAS  Google Scholar 

  7. Close TJ, Fenton RD, Yang A, Asghar R, DeMason DA, Crone DE, Meyer NC and Moonan F (1993) Dehydrin: The Protein. In: Close TJ and Bray EA (eds) Plant Responses to Cellular Dehydration During Environmental Stress. Amer Soc Plant Physiol, pp 104–118

    Google Scholar 

  8. Covarrubias AA, Ayala JW, Reyes JL, Hernandez M and Garciarrubio A (1995) Cell-wall proteins induced by water deficit in bean (Phaseolus vulgaris L.) seedlings. Plant Physiol 107: 1119–1128

    PubMed  CAS  Google Scholar 

  9. Creelman RA and Mullet JE (1991) Water deficit modulates gene expression in growing zones of soybean seedlings. Analysis of differentially expressed cDNAs, a new ß-tubulin gene, and expression of genes encoding cell wall proteins. Plant Mol Biol 17: 591–608

    Article  PubMed  CAS  Google Scholar 

  10. Creelman RA, Mason HS, Bensen RJ, Boyer JS and Mullet JE (1990) Water deficit and abscisic acid cause differential inhibition of shoot versus root growth in soybean seedlings. Analysis of growth, sugar accumulation, and gene expression. Plant Physiol 92: 205–214

    Google Scholar 

  11. Crowe JH, Crowe LM, Leslie SB and Fisk E (1993) Mechanisms of stabilization of dry biomolecules in anhydrobiotic organisms. In: T. J. Close TJ and E. A. Bray EA (eds) Plant Responses to Cellular Dehydration During Environmental Stress. Amer Soc Plant Physiol, pp 11–20

    Google Scholar 

  12. Demmig B, Winter K, Krüger A and Czygan F-C (1988) Zeaxanthin and the heat dissipation of excess light energy in Neri-um oleander exposed to a combination of high light and water stress. Plant Physiol 87: 17–24

    Article  PubMed  CAS  Google Scholar 

  13. Dure L, III (1993) Structural motifs in lea proteins. In: Close TJ and Bray EA (eds) Plant Responses to Cellular Dehydration During Environmental Stress. Amer Soc Plant Physiol, pp 91103

    Google Scholar 

  14. Guerrero FD, Jones JT and Mullet JE (1990) Turgor-responsive gene transcription and RNA levels increase rapidly when pea shoots are wilted. Sequence and expression of three inducible genes. Plant Mol Biol 15: 11–26

    Google Scholar 

  15. Hanson AD (1993) Accumulation of quaternary ammonium and tertiary sulfonium compounds. In: Close TJ and Bray EA (eds) Plant Responses to Cellular Dehydration During Environmental Stress. Amer Soc Plant Physiol, pp 30–36

    Google Scholar 

  16. Hanson AD and Hitz WD (1982) Metabolic responses of mesophytes to plant water deficits. Ann Rev Plant Physiol 33: 163–203

    Article  CAS  Google Scholar 

  17. Hsiao TC and Jing J (1987) Leaf and root expansive growth in response to water deficits. In: Cosgrove DJ and Knievel DP (eds) Physiology of Cell Expansion During Plant Growth. Amer Soc Plant Physiol, pp 180–192

    Google Scholar 

  18. Jones ME and Turner MC (1978) Osmotic adjustment in leaves of sorghum in response to water deficits. Plant Physiol 61: 122126

    Google Scholar 

  19. Loescher WH (1987) Physiology and metabolism of sugar alcohols in higher plants. Physiol Plantarum 70: 553–557

    Article  CAS  Google Scholar 

  20. Ludlow MM and Muchow RC (1990) A critical evaluation of traits for improving crop yields in water-limited environments. Advances in Agronomy 43: 107–153

    Article  Google Scholar 

  21. Mason HS, Mullet JE and Boyer JS (1988) Polysomes, messenger RNA, and growth in soybean stems during development and water deficit. Plant Physiol 86: 725–733

    Article  PubMed  CAS  Google Scholar 

  22. Mason HS and Mullet JE (1990) Expression of two soybean vegetative storage protein genes during development and in response to water deficit, wounding, and jasmonic acid. The Plant Cell 2: 569–579

    PubMed  CAS  Google Scholar 

  23. Mason HS, DeWald DB, Creelman RA and Mullet JE (1992) Coregulation of soybean vegetative storage protein gene expression by methyl jasmonate and soluble sugars. Plant Physiol 98: 859–867

    Article  PubMed  CAS  Google Scholar 

  24. Miao G-H, Hong Z and Verma DPS (1992) Topology and phosphorylation of soybean nodulin-26, an intrinsic protein of the peribacteriod membrane. J Cell Biol 118: 481–490

    Article  PubMed  CAS  Google Scholar 

  25. Miller KJ, Kennedy EP and Reinhold VN (1986) Osmotic adaptation by gram-negative bacteria: possible role for periplasmic oligosaccharides. Science 231: 48–51

    Article  PubMed  CAS  Google Scholar 

  26. Morgan JM (1983) Osmoregulation as a selection criterion for drought tolerance in wheat. Aust J Agric Res 34: 607–614

    Article  Google Scholar 

  27. Mullet JE (1990) Reversible inhibition of hypocotyl growth in soybean seedlings exposed to water deficit. Plant Gene Transfer, pp 249–256, Alan R. Liss, Inc.

    Google Scholar 

  28. Nakanishi T, Turner RJ and Burg MB (1989) Osmoregulation changes in myo-inositol transport by renal cells. Proc Natl Acad Sci USA 86: 6002–6006

    Article  PubMed  CAS  Google Scholar 

  29. Nonami H and Boyer JS (1990) Primary events regulating stem growth at low water potentials. Plant Physiol 94: 1601–1609

    Article  Google Scholar 

  30. Nonami H and Boyer JS (1990) Wall extensibility and cell hydraulic conductivity decrease in enlarging stem tissues at low water potentials. Plant Physiol 93: 1610–1619

    Article  PubMed  CAS  Google Scholar 

  31. Oliver MJ (1991) Influence of protoplasmic water loss on the control of protein synthesis in the desiccation-tolerant moss Tortula ruralis. Plant Physiol 97: 1501–1511

    Article  PubMed  CAS  Google Scholar 

  32. Piatkowski D, Schneider K, Salamini F and Bartels D (1990) Characterization of five abscisic acid-responsive cDNA clones isolated from the desiccation-tolerant plant Craterostigma plantagineum and their relationship to other water-stress genes. Plant Physiol 94: 1682–1688

    Article  PubMed  CAS  Google Scholar 

  33. Preston GM, Jung JS, Guggino WB and Agre P (1993) The mercury-sensitive residue at cysteine 189 in the CHIP28 water channel. J Biol Chem 268: 17–20

    PubMed  CAS  Google Scholar 

  34. Reizer J, Reizer A and Saier MH Jr (1993) The MIP family of integral membrane channel proteins: sequence comparisons, evolutionary relationships, reconstructed pathway of evolution, and proposed functional differentiation of the two repeated halves of the proteins. Critical Rev. Biochem Molec Biol 28: 235–257

    Google Scholar 

  35. Sweet G, Gandor C, Voegele R, Wittekindt N, Beuerle J, Truniger V, Lin ECC and Boos W (1990) Glycerol facilitator of Escherichia coli: cloning of glpF and identification of the glpF product. J Bacteriol 172: 424–430

    PubMed  CAS  Google Scholar 

  36. Verkman AS (1992) Water channels in cell membranes. Annu Rev Physiol 54: 97–108

    Article  PubMed  CAS  Google Scholar 

  37. Voetberg GS and Sharp RE (1991) Growth of the maize primary root at low water potentials. III. Role of increased praline deposition in osmotic adjustment. Plant Physiol 96: 1125–1130

    Article  PubMed  CAS  Google Scholar 

  38. Yamaguchi-Shinozaki K, Koizumi M, Urao S and Shinozaki K (1992) Molecular cloning and characterization of 9 cDNAs for genes that are responsive to desiccation in Arabidopsis thaliana: sequence analysis of one cDNA clone that encodes a putative transmembrane channel protein. Plant Cell Physiol 33: 217–224

    CAS  Google Scholar 

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© 1996 Springer Science+Business Media Dordrecht

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Mullet, J.E., Whitsitt, M.S. (1996). Plant cellular responses to water deficit. In: Belhassen, E. (eds) Drought Tolerance in Higher Plants: Genetical, Physiological and Molecular Biological Analysis. Springer, Dordrecht. https://doi.org/10.1007/978-94-017-1299-6_6

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  • DOI: https://doi.org/10.1007/978-94-017-1299-6_6

  • Publisher Name: Springer, Dordrecht

  • Print ISBN: 978-90-481-4721-2

  • Online ISBN: 978-94-017-1299-6

  • eBook Packages: Springer Book Archive

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