Skip to main content
Log in

Molecular characterization of XVT8, a stress-responsive gene from the resurrection plant Xerophyta viscosa Baker

  • Published:
Plant Growth Regulation Aims and scope Submit manuscript

Abstract

Xerophyta viscosa (Baker) is a monocotyledonousresurrection plant that is capable of tolerating extremes of desiccation. Uponrewatering, it rehydrates completely, assuming its full physiologicalactivities. Studies on changes in gene expression associated with dehydrationstress tolerance were conducted. A cDNA library was constructed from mRNAisolated from dehydrated X. viscosa leaves [85%,37% and 5% relative water content (RWC)].XVT8 represents one of 30 randomly selected clones thatwere differentially expressed when X. viscosa wasdehydrated. Sequence analysis of XVT8 revealed thatXVT8 exhibited 45% and 43% identity todehydrin proteins from Arabidopsis thaliana andPisum sativum respectively, at the amino acid level.XVT8 encodes a glycine -rich protein (27 kDa)which is largely hydrophilic and contains a hydrophobic segment at theC-terminus. Southern blot analysis confirmed the presence ofXVT8 in the X. viscosa genome.XVT8 transcripts accumulated in X.viscosa plants that were exposed to heat, low temperature anddehydration stresses, and to exogenous abscisic acid and ethylene. Theseresultsprovide direct evidence for the heat, low temperature, dehydration, abscisicacid and ethylene -dependent regulation of the XVT8 geneinX. viscosa.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Altschul S.F., Gish W., Miller W., Meyers E.W. and Lipman D.J. 1990. Basic local alignment search tool. J.Mol.Biol. 215: 403–410.

    Google Scholar 

  • Atwell B.J., Drew M.C. and Jackson M.B. 1988. The influence of oxygen deficiency on ethylene synthesis, 1-aminocyclopropane-1-carboxylic acid levels and aerenchyma formation in roots of Zea mays L. Physiol. Plant. 72: 15–22.

    Google Scholar 

  • Black M., Corbineau F., Gee H. and Come D. 1999. Water content, raffinose and dehydrins in the induction of desiccation tolerance in immature wheat embryos. Plant Physiol. 120: 463–471.

    Google Scholar 

  • Blackman S.A., Wetlaufer S.H., Obendorf R.L. and Leopold A.C. 1991. Maturation proteins associated with desiccation tolerance in soybean. Plant Physiol. 96: 868–874.

    Google Scholar 

  • Blackman S.A., Obendorf R.L. and Leopold A.C. 1992. Maturation proteins and sugars in desiccation tolerance of developing soybean seeds. Plant Physiol. 100: 225–230.

    Google Scholar 

  • Bewely J.D. and Oliver M.J. 1992. Desiccation-tolerance in vegetative plant tissues and seeds: Protein synthesis in relation to desiccation and a potential role for protection and repair mechanisms. In: Somero G.N., Osmond C.B. and Bolis C.L. (eds), Water and Life: A Comparative Analysis ofWater Relationships at the Organismic, Cellular and Molecular Levels. Springer-Verlag, pp. 141–160.

  • Bewely J.D., Reynolds T.L. and Oliver M.J. 1993. Evolving strategies in the adaptation of desiccation. In: Close T.J. and Bray E.A. (eds), Plant Responses to Cellular Dehydration During Environmental Stress. Current Topics in Plant Physiology., pp. 193–201.

  • Bonhert H.J., Nelson D.E. and Jensen R.G. 1995. Adaptation to environmental stresses. The Plant Cell. 7: 1099–1034.

    Google Scholar 

  • Bray E.A. 1993. Molecular Responses toWater Deficit. Plant Physiol. 103: 1035–1040.

    Google Scholar 

  • Bray E.A. 1997. Plant Responses to Water Deficit. Molec. Plant Sci. 2: 48–54.

    Google Scholar 

  • Chomczynski P. 1987. Single step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Analytical Biochemistry. 162: 156–159.

    Google Scholar 

  • Close T.J., Fenton R.D., Yang A., Asghar R., DeMason D.A., Crone D.E. et al. 1993. Dehydrin: the protein. In: Close, T.J. and Bray E.A. (eds), Response of Plants to Cellular Dehydration During Environmental Stress. American Society for Plant Physiology, Rockville, pp. 104–118.

    Google Scholar 

  • Close T.J. 1996. Dehydrins: Emergence of a biochemical role of a family of plant dehydration proteins. Plant Physiol. 97: 795–803.

    Google Scholar 

  • Cohen A., Moses, M.S. and Bray E.A. 1991. Organ-specific and Environmentally Regulated Expression of two Abscisic Acidinduced Genes of Tomato. Plant Physiol. 97: 1367–1374.

    Google Scholar 

  • Conley T.R., Sharp R.E. and Walker J.C. 1997. Water Deficit Rapidly stimulates the Activity of a protein Kinase in the Elongation zone of the Maize Binary Root. Plant Physiol. 113: 219–226.

    Google Scholar 

  • Dace H., Sherwin H.W. and Farrant J.M. 1998. Use of metabolic inhibitors to elucidate mechanisms of recovery from desiccation stress in the resurrection plant Xerophyta humilis. Plant Growth Regulation 24: 171–178.

    Google Scholar 

  • Dellaporta S., Wood J. and Hicks J.B. 1983. A Plant DNA Minipreparation: Version II. Plant Molecular Biology Reporter 1(4): 19–21.

    Google Scholar 

  • Drew M.C. 1997. Oxygen deficiency and root metabolism: injury and acclimation under hypoxia and anoxia. Ann. Rev. Plant Physiol. Plant Mol. Biol. 48: 223–250.

    Google Scholar 

  • Dure L., Crouch M., Harada J., Ho T.-H.D., Mundy J., Quatrano R. et al. 1989. Common amino acid sequence domains among the LEA proteins of higher plants. Plant Mol. Biol. 12: 475–486.

    Google Scholar 

  • Dure L. 1993. Structural motifs in LEA proteins in higher plants. In: Close T.J. and Bray E.A. (eds), Response of Plants to Cellular Dehydration During Environmental Stress. American Society for Plant Physiology, Rockville, pp. 104–118.

    Google Scholar 

  • Gaff D.F. 1971. Desiccation-tolerant flowering plants in Southern Africa. Science 174: 1033–1034.

    Google Scholar 

  • Galau G.A., Hughes D.W. and Dure L. 1986. Abscisic Acid induction of cloned cotton late embryogenesis-abundant (Lea) mRNAs. Plant Mol. Biol. 7: 155–170.

    Google Scholar 

  • Galau G.A., Bijaisorodat N. and Hughes D.W. 1987. Accumulation kinetics of cotton late embryogenesis-abundant (Lea) mRNA and storage of protein mRNAs: coordinate regulation during embryogenesis and the role of abscisic acid. Dev. Biol. 123: 198–212.

    Google Scholar 

  • Gee O.H., Probert R.J. and Coomber S.A. 1994. 'Dehydrin-like’ proteins and desiccation tolerance in seeds. Seed Sci Res. 4: 135–141.

    Google Scholar 

  • Han B., Hughes D.W., Galau G.A., Bewely J.D. and Chermidae A.R. 1997. Changes in late-embryogenesis-abundant (LEA) messenger RNase and dehydrins during maturation and premature drying of Ricinus communis L. seeds. Plant. 201: 27–35.

    Google Scholar 

  • He J.C., Finlay son S.A., Drew M.C., Jordan W.R. and Morgan P.I. 1996. Ethylene biosynthesis during aerenchyma formation in roots of Zea mays subjected to mechanical impedance and hypoxia. Plant Physiol. 112: 1679–1685.

    Google Scholar 

  • Ingram I. and Bartels D. 1996. The molecular basis of dehydration tolerance in plants. Annu. Rev. Plant Physiol. 88: 829–832.

    Google Scholar 

  • Chermidae A.R. 1997. Approaches to elucidate the basis of desiccation-tolerance in seeds. Seed Sci. Res. 7: 75–95.

    Google Scholar 

  • Kyte J. and Doolittle R.F. 1982. A simple method for displaying the hydropathic character of a protein. J.Mol.Biol. 157: 105–132.

    Google Scholar 

  • Lang V. and Palva E.T. 1992. 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.

    Google Scholar 

  • Mundy J. and Chua N.-H. 1988. Abscisic acid and water-stress induce the expression of a novel rice. EMBO J. 7: 2279–2286.

    Google Scholar 

  • Nelson D., Salamini F. and Bartels D. 1994. Abscisic acid promotes novel DNA-binding activity to a desiccation-related promoter of Craterostigma plantagineum. Plant J. 5: 451–458.

    Google Scholar 

  • Oliver M.J. and Bewely J.D. 1997. Desiccation-tolerance of plant tissues: a mechanistic overview. Horticultural reviews 18: 171–213.

    Google Scholar 

  • Reynolds T.L. and Bewely J.D. 1993a. Characterization of protein synthetic changes in a desiccation-tolerant fern Polypodium virginianum. Comparison of the effects of drying, rehydration and abscisic acid. J. Exp. Bot. 44: 921–928.

    Google Scholar 

  • Robertson M. and Chandler P.M. 1994. A dehydrin cognate protein from pea (Pisum sativum) with an atypical pattern of expression. Plant Mol. Biol. 26: 805–816.

    Google Scholar 

  • Russouw P.S., Farrant J.M., Brandt W., Maeder D. and Lindsey G.G. 1995. Isolation and characterization of a heat soluble protein from pea (Pisum sativum). Seed Sci. Res. 5: 137–144.

    Google Scholar 

  • Sambrook J., Fritsch E.F. and Maniatis T. 1989. In molecular cloning: A laboratory manual. 2nd edn. Cold Spring Harbor Lab. Press, Plainview, NY.

    Google Scholar 

  • Sherwin H.W. and Farrant J.M. 1996. Differences in rehydration of three desiccation-tolerant angiosperm species. Annals of Botany 78: 703–710.

    Google Scholar 

  • Short J.M., Fernandez, J.M., Sorge, J.A. and Huse, W.D. 1988. Lambda ZAP: A bacteriophage lambda expression vector with in vivo excision properties. Nucleic Acids Research 16: 7583–7600.

    Google Scholar 

  • Siddiqui N.U., Chung H.-J., Thomas T.L. and Drew M.C. 1998. Abscisic acid-dependent and-independent expression of the carrot late-embryogenesis-abundant-class gene Dc3 in transgenic tobacco seedlings. Plant Physiol. 118: 1181–1190.

    Google Scholar 

  • Swire-Clark G.A. and Meacock P.A. 1990. The wheat LEA protein Em functions as an osmoprotective molecule in Saccharomces cerevisiae. Plant Mol. Biol. 37: 513–521.

    Google Scholar 

  • Vertucci C.W. and Farrant J.M. 1995. Acquisition and loss of desiccation tolerance. In: Kigel J. and Galili G. (eds), Seed Germination. Marcel Dekker, New York, pp. 237–271.

    Google Scholar 

  • Xu V., Duan X., Wang B., Hong B., Ho T.D. and Wu R. 1996. Expression of a Late Embryogenesis Abundant Protein Gene, HVA 1, from Barley Confers to Tolerance to Water-deficit and Salt Stress in Transgenic Rice. Plant. Physiol.110: 249–257.

    Google Scholar 

  • Walford S.-A.1998. Dissertation for Honours: Studies on a cDNA encoding an aldose reductase from the resurrection plant Xerophyta viscosa. University of Cape Town, Rondebosch.

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ndima, T., Farrant, J., Thomson, J. et al. Molecular characterization of XVT8, a stress-responsive gene from the resurrection plant Xerophyta viscosa Baker. Plant Growth Regulation 35, 137–145 (2001). https://doi.org/10.1023/A:1014433821730

Download citation

  • Issue Date:

  • DOI: https://doi.org/10.1023/A:1014433821730

Keywords

Navigation