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Overexpression of wheat dehydrin DHN-5 enhances tolerance to salt and osmotic stress in Arabidopsis thaliana

  • Biotic and Abiotic Stress
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Abstract

Late Embryogenesis Abundant (LEA) proteins are associated with tolerance to water-related stress. A wheat (Triticum durum) group 2 LEA proteins, known also as dehydrin (DHN-5), has been previously shown to be induced by salt and abscisic acid (ABA). In this report, we analyze the effect of ectopic expression of Dhn-5 cDNA in Arabidopsis thaliana plants and their response to salt and osmotic stress. When compared to wild type plants, the Dhn-5 transgenic plants exhibited stronger growth under high concentrations of NaCl or under water deprivation, and showed a faster recovery from mannitol treatment. Leaf area and seed germination rate decreased much more in wild type than in transgenic plants subjected to salt stress. Moreover, the water potential was more negative in transgenic than in wild type plants. In addition, the transgenic plants have higher proline contents and lower water loss rate under water stress. Also, Na+ and K+ accumulate to higher contents in the leaves of the transgenic plants. Our data strongly support the hypothesis that Dhn-5, by its protective role, contributes to an improved tolerance to salt and drought stress through osmotic adjustment.

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References

  • Babu RC, Zhang J, Blum A, Ho DTH, Wu R, Nguyen HT (2004) HVA1, a LEA gene from barley confers dehydration tolerance in transgenic rice (Oryza sativa L.) via cell membrane protection. Plant Sci 166:855–862

    Article  CAS  Google Scholar 

  • Baker J, Steele C, Dure L III (1988) Sequence and characterization of 6 LEA proteins and their genes from cotton. Plant Mol Biol 11:277–291

    Article  CAS  Google Scholar 

  • Bates LS, Waldren RP, Teeare ID (1973) Rapid determination of free Pro for water-stress studies. Plant Soil 39:205–207

    Article  CAS  Google Scholar 

  • Bray EA (1993) Molecular responses to water deficit. Plant Physiol 103:1035–1040

    PubMed  CAS  Google Scholar 

  • Bray EA, Bailey-Serres J, Weretilnyk E (2000) Responses to abiotic stresses. In: Buchanan B, Gruissem W, Jones R (eds) Biochemistry and molecular biology of plants. American Society of Plant Physiologists, pp 1158–1176

  • Brini F, Hanin M, Lumbreras V, Irar S, Pagès M, Masmoudi K (2007) Functional characterization of DHN-5, a dehydrin showing a differential phosphorylation pattern in two Tunisian durum wheat (Triticum durum Desf.) varieties with marked differences in salt and drought tolerance. Plant Sci 172:20–28

    Article  CAS  Google Scholar 

  • Close TJ (1996) Dehydrins: emergence of a biochemical role of a family of plant dehydration proteins. Physiol Plant 97:795–803

    Article  CAS  Google Scholar 

  • Close TJ (1997) Dehydrins: a commonalty in the response of plants to dehydration and low temperature. Physiol Plant 100:291–296

    Article  CAS  Google Scholar 

  • Clough SJ, Bent AF (1998) Floral dip: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana. Plant J 16:735–743

    Article  PubMed  CAS  Google Scholar 

  • Delauney AJ, Hu CA, Kishor PB, Verma DP (1993) Cloning of ornithine delta-aminotransferase cDNA from Vigna aconitifolia by trans-complementation in Escherichia coli and regulation of proline biosynthesis. J Biol Chem 268:18673–18678

    PubMed  CAS  Google Scholar 

  • Dure L (1993) A repeating 11-mer amino acid motif and plant desiccation. Plant J 3:363–369

    Article  PubMed  CAS  Google Scholar 

  • Dure L, Crouch M, Harada J, Ho THD, Mundy J, Quatrano R, Thomas T, Sung ZR (1989) Common amino acids sequence domains among the LEA proteins of higher plants. Plant Mol Biol 12:475–486

    Article  CAS  Google Scholar 

  • Figueras M, Pujal J, Saleh A, Savè R, Pagès M, Goday A (2004) Maize Rab17 over-expression in Arabidopsis plants promotes osmotic stress tolerance. Ann Appl Biol 144:251–257

    Article  CAS  Google Scholar 

  • Goday A, Sanchez-Martinez D, Gomez J, Puigdomenech P, Pages M (1988) Gene expression in developing Zea mays embryos: regulation by abscisic acid of a highly phosphorylated 23–25 kD group of protein. Plant Physiol 88:564–569

    Article  PubMed  CAS  Google Scholar 

  • Goday A, Jensen AB, Culianez-Macià FA, Albà MM, Figueras M, Serratosa J, Torrent M, Pagès M (1994) The maize abscissic acid-responsive protein Rab17 is located in the nucleus and interacts with nuclear localization signals. Plant Cell 6:351–360

    Article  PubMed  CAS  Google Scholar 

  • Gunasekera D, Berkowitz GA (1992) Evaluation of contrasting cellular-level acclimation responses to leaf water deficits in three wheat genotypes. Plant Sci 86:1–12

    Article  Google Scholar 

  • Gupta SA, Berkowitz GA (1987) Osmotic adjustment, symplast volume, and nonstomatally mediated water stress inhibition of photosynthesis in wheat. Plant Physiol 89:1040–1047

    Google Scholar 

  • Holmström KO, Mäntylä E, Welin R, Mandal A, Palva T (1996) Drought tolerance in tobacco. Nature 379:683–684

    Article  Google Scholar 

  • Honjoh KI, Oda Y, Tkata R, Miyamoto T, Hatano S (1999) Introduction of the hiC6 gene, which encodes a homologue of a late embryogenesis abundant (LEA) protein, enhances freezing tolerance of yeast. J Plant Physiol 155:509–512

    CAS  Google Scholar 

  • Imai R, Chang L, Ohta A, Bray E, Takagi M (1996) A lea gene of tomato confers salt and freezing tolerance when expressed in Saccharomyces cerevisae. Gene 170:243–248

    Article  PubMed  CAS  Google Scholar 

  • Ingram J, Bartels D (1996) The molecular basis of dehydration tolerance in plants. Annu Rev Plant Physiol Plant Mol Biol 47:377–403

    Article  PubMed  CAS  Google Scholar 

  • Ismail AM, Hall AE, Close TJ (1999) Purification and partial characterization of a dehydrin involved in chilling tolerance during seedling emergence of cowpea. Plant Physiol 120:237–244

    Article  PubMed  CAS  Google Scholar 

  • Iturriaga G, Schneider K, Salamini F, Bartels D (1992) Expression of desiccation-related proteins from the resurrection plant Craterostigma plantagineum in transgenic tobacco. Plant Mol Biol 20:555–558

    Article  PubMed  CAS  Google Scholar 

  • Johnson RC, Mornhinweg DW, Ferris DM, Heithol JJ (1987) Leaf photosynthesis and conductance of selected Triticum species at different water potentials. Plant Physiol 83:1014–1017

    PubMed  Google Scholar 

  • Kawasaki S, Borchert C, Deyholos M, Wang H, Brazille S, Kawai K, Galbraith D, Bohnert HJ (2001) Gene expression profiles during the initial phase of salt stress in rice. Plant Cell 13(4):889–905

    Article  PubMed  CAS  Google Scholar 

  • Koag MC, Fenton RD, Wilkens S, Close TJ (2003) The binding of maize DHN1 to lipid vesicles. Gain of structure and lipid specificity. Plant Physiol 131:309–316

    Article  PubMed  CAS  Google Scholar 

  • Kobayashi N, Horikoshi T, Katsuyama H, Takashi H, Takayanagi K (1998) A simple and efficient DNA extraction method for plants, especially woody plants. Plant Tissue Cult Biotechnol 4:76–80

    Google Scholar 

  • Mahajan S, Tuteja N (2005) Cold, salinity and drought stresses: an overview. Arch Biochem Biophys 444:139–158

    Article  PubMed  CAS  Google Scholar 

  • Morgan JM (1984) Osmoregulation and water stress in higher plants. Aust J Agric Res 35:299–319

    Google Scholar 

  • Munns R (2005) Genes and salt tolerance: bringing them together. New Phytol 167:645–663

    Article  PubMed  CAS  Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bioassay with tobacco tissue cultures. Physiol Plant 15:473–497

    Article  CAS  Google Scholar 

  • Nanjo T, Kobayashi M, Yoshiba Y, Sanada Y, Wada K, Tsukaya H, Kakubari Y, Yamaguchi-Shinozaki K, Shinozaki K (1999) Biological functions of proline in morphogenesis and osmotolerance revealed in antisense transgenic Arabidopsis thaliana. Plant J 18:185–193

    Article  PubMed  CAS  Google Scholar 

  • Park BJ, Liu Z, Kanno A, Kameya T (2005) Genetic improvement of Chinese cabbage for salt and drought tolerance by constitutive expression of a B. napus LEA gene. Plant Sci 169:553–558

    Article  CAS  Google Scholar 

  • Pilon-Smits E, Ebskamp M, Paul MJ, Weissbeek M, Smeekens S (1995) Improved performance of transgenic fructan-accumulating tabacco under drought stress. Plant Physiol 107:125–130

    PubMed  CAS  Google Scholar 

  • Radin JW (1983) Physiological consequences of cellular water deficits: Osmotic adjustment. In: Taylor HM, Jordan WR, Sinclair TR (eds) Limitation of efficient water use in crop production. Am Soc Agron, pp 227–288

  • Romero C, Bellés JM, Vayá JL, Serrano R, Culiáñez-Macià FA (1997) Expression of the yeast trehalose-6-phosphate synthase in transgenic tobacco plants: pleiotropic phenotypes include drought tolerance. Planta 201:293–297

    Article  CAS  PubMed  Google Scholar 

  • Saavedra L, Svensson J, Carballo V, Izmendi D, Wellin B, Vidal S (2006) A dehydrin gene in Physcomitrella patens is required for salt and osmotic stress tolerance. Plant J 45:237–249

    Article  PubMed  CAS  Google Scholar 

  • Shen B, Hohmann S, Jensen RG, Bohnert H (1999) Roles of sugar alcohols in osmotic stress adaptation. Replacement of glycerol by mannitol and sorbitol in yeast. Plant Physiol 121:45–52

    Article  PubMed  CAS  Google Scholar 

  • Sivamani E, Bahieldin A, Wraith JM, Al-Niemi T, Dyer WE, Ho THD, Wu R (2000) Improved biomass productivity and water use efficiency under water-deficit conditions in transgenic wheat constitutively expressing the barley HVA1 gene. Plant Sci 155:1–9

    Article  PubMed  CAS  Google Scholar 

  • Swire-Clark GA, Marcotte WR Jr (1999) The wheat LEA protein Em functions as an osmoprotective molecule in Saccharomyces cerevesiae. Plant Mol Biol 39:117–128

    Article  PubMed  CAS  Google Scholar 

  • Tarczynski MC, Jensen RG, Bohnert H (1993) Stress protection of transgenic tobacco by production of the osmolyte mannitol. Science 259:508–510

    Article  PubMed  CAS  Google Scholar 

  • Xu D, Duan X, Wang B, Hong B, Ho TD, Wu R (1996) Expression of a late embryogenesis abundant protein gene, HVA1, from barley confers tolerance to water deficit and salt stress in transgenic rice. Plant Physiol 110:249–257

    PubMed  CAS  Google Scholar 

  • Yu LX, Setter TL (2003) Comparative transcriptional profiling of placenta and endosperm in developing maize kernels in response to water deficit. Plant Physiol 131:568–582

    Article  PubMed  CAS  Google Scholar 

  • Zhu JK (2002) Salt and drought stress signal transduction in plants. Annu Rev Plant Biol 53:247–273

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

This work was supported jointly by grants from the Ministry of Higher Education, Scientific Research and Technology, Tunisia and the Agence Espagnole de cooperation Internationale (AECI) Officina Técnica de Cooperación, Spain. Authors are grateful to Prof. Barbara Hohn for critical reading of this manuscript and Dr. Ahmed Rebaï for statistical analysis.

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Correspondence to Khaled Masmoudi.

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Communicated by J. Zou.

Faïçal Brini and Moez Hanin have contributed equally to this work.

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Brini, F., Hanin, M., Lumbreras, V. et al. Overexpression of wheat dehydrin DHN-5 enhances tolerance to salt and osmotic stress in Arabidopsis thaliana . Plant Cell Rep 26, 2017–2026 (2007). https://doi.org/10.1007/s00299-007-0412-x

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  • DOI: https://doi.org/10.1007/s00299-007-0412-x

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