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Differential expression of heat shock protein and alteration in osmolyte accumulation under heat stress in wheat

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Abstract

Heat stress causes an array of physiological, biochemical and morphological changes in plants, affecting growth and yield. Here, we report cloning of HSP90 gene of 2,323 bp from C-306 cultivar of wheat having ORF from 62 to 2,164 bp encoded for 700 amino acids. Quantitative real time expression analysis of HSP90 gene in C-306 showed 1.5, 1.2, 2.5 fold (in root), 4.5, 4.3 and 6.5 fold increase (in flag leaf) in the transcript level at pollination, milky dough and seed hardening stages. HSP90 transcript level was observed low in root as well as shoot of susceptible cultivar (PBW343) at different stages of growth. A significant difference in the fold expression of HSP90 was observed in C-306 and PBW343 against differential heat shock. An altered expression of H2O2 and decline in proline accumulation was observed in C-306 at different stages of growth. Western blot analysis revealed the presence of 5, 6 and 5 multiprotein chaperone complexes of HSP90 in the range of 95 Da to 70 KDa at pollination, milky dough and seed hardening stages. An expression of few novel isoenzymes of superoxide dismutase and catalase was observed against differential heat shock. A decrease in cell membrane stability was observed at different stages of growth in C-306 cultivar of wheat. In conclusion, we suggest that a high HSP90 transcript level along with high activities of antioxidant isoenzymes and low proline accumulation is a promising target for developing wheat genotypes with tolerance to heat stress.

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Abbreviations

CAT:

Catalase

SOD:

Superoxide dismutase

HS:

Heat stress

HSP:

Heat shock protein

ROS:

Reactive oxygen species

References

  • Assad MT, Paulsen GM (2002) Genetic changes in resistance to environment stress by U.S. great Plains wheat cultivars. Euphytica 128:87–96

    Article  CAS  Google Scholar 

  • Bandurska H (1993) In vitro and In vivo effect of proline on nitrate reductase activity under osmotic stress in barley. Acta Physiol Plant 15:83–88

    CAS  Google Scholar 

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

    Article  CAS  Google Scholar 

  • Blum A, Ebercon A (1981) Cell membrane stability as a measure of drought and heat tolerance in wheat. Crop Sci J 21:43–47

    Article  Google Scholar 

  • Bohnert HJ, Jensen RG (1996) Strategies for engineering water-stress tolerance in plants. Trends Biotechnol 14:89–97

    Article  CAS  Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein dye binding. Anal Biochem 72:248–254

    Article  PubMed  CAS  Google Scholar 

  • Cheeseman JM (2006) Hydrogen peroxide concentrations in leaves under natural conditions. J Exp Bot 57:2435–2444

    Article  PubMed  CAS  Google Scholar 

  • Chen S, Smith DF (1998) Hop as an adaptor in the heat shock protein 70 (Hsp70) and hsp90 chaperone machinery. J Biol Chem 273:35194–35200

    Article  PubMed  CAS  Google Scholar 

  • Clement M, Leonhardt N, Droillard M, Reiter I, Montillet J, Genty B, Lauriere C, Nussaume L, Noel LD (2011) The cytosolic/nuclear HSC70 and HSP90 molecular chaperones are important for stomatal closure and modulate abscisic acid-dependent physiological responses in Arabidopsis. Plant Physiol. doi:10.1104/pp. 111.174425

  • Feder ME, Hoffman GE (1999) Heat-shock proteins, molecular chaperones, and the stress response: evolutionary and ecological physiology. Annu Rev Physiol 61:243–282

    Article  PubMed  CAS  Google Scholar 

  • Fokar M, Blum A, Nguyen HT (1998) Heat tolerance in spring wheat. II. Grain filling. Euphytica 104:9–15

    Article  Google Scholar 

  • Hare PD, Cress WA (1997) Metabolic implications of stress-induced proline accumulation in plants. Plant Growth Regul 21:79–102

    Article  CAS  Google Scholar 

  • Hua X, Weitao LV, Lin B, Zhang M (2011) Proline accumulation is inhibitory to Arabidopsis seedlings during heat stress. Plant Physiol. doi:10.1104/pp. 111.175810

  • Kele Y, Oncel I (2002) Response of antioxidative defence system to temperature and water stress combinations in wheat seedlings. Plant Sci 163:783–790

    Article  Google Scholar 

  • Laemmli UK (1970) Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685

    Article  PubMed  CAS  Google Scholar 

  • Larkindale J, Knight MR (2002) Protection against heat stress-induced oxidative damage in Arabidopsis involves calcium, abscisic acid, ethylene, and salicylic acid. Plant Physiol 128:682–695

    Article  PubMed  CAS  Google Scholar 

  • Loreto F, Velikova V (2001) Isoprene produced by leaves protects the photosynthetic apparatus against ozone damage, quenches ozone products, and reduces lipid peroxidation of cellular membranes. Plant Physiol 127:1781–1787

    Article  PubMed  CAS  Google Scholar 

  • Mazhar H, Basha SM (2002) Effects of desiccation on peanut (Arachis hypogea L.) seed protein composition. Environ Exp Bot 47:67–75

    Article  CAS  Google Scholar 

  • Morita S, Kaminaka H, Masumura T, Tanaka K (1999) Induction of rice cytosolic ascorbate peroxidase mRNA by oxidative stress; the involvement of hydrogen peroxide in oxidative stress signaling. Plant Cell Physiol 40:417–422

    Article  CAS  Google Scholar 

  • Muessig C, Fischer S, Altmann T (2002) Brassinosteroid-regulated gene expression. Plant Physiol 129:1241–1251

    Article  Google Scholar 

  • Ozden M, Demirel U, Kahraman A (2009) Effects of proline on antioxidant system in leaves of grapevine (Vitis vinifera L.) exposed to oxidative stress by H2O2. Sci Hortic 119(2):163–168

    Article  CAS  Google Scholar 

  • Roychaudhari G, Sarath M, Zeece MJ (2003) Reversible denaturation of soyabean kunitz trypsin inhibitor. Arch Biochem Biophys 412:20–26

    Article  Google Scholar 

  • Roy SK, Hiyama T, Nakamoto H (1999) Purification and characterization of the 16-kDa heat-shock-responsive protein from the thermophilic cyanobacterium Synechococcus vulcanus, which is an α-crystallin-related, small heat shock protein. Eur J Biochem 262:406–416

    Article  PubMed  CAS  Google Scholar 

  • Rucinska R, Waplak S, Gwozdz EA (1999) Free radical formation and activity of antioxidant enzymes in lupin roots exposed to lead. Plant Physiol Biochem 37:113–115

    Article  Google Scholar 

  • Rizhsky L, Liang H, Shuman J, Shulaev V, Davletova S, Mitler R (2004) When defense pathways collide: the response of Arabidopsis to a combination of drought and heat stress. Plant Physiol 134:1683–1696

    Article  PubMed  CAS  Google Scholar 

  • Saadalla MM, Shanahan JF, Quick JS (1990) Heat tolerance in winter wheat: I. Hardening and genetic effects on membrane thermostability. Crop Sci 30:1243–1247

    Article  Google Scholar 

  • Sairam RK, Srivastava GC (2000) Induction of oxidative stress and antioxidant activity by hydrogen peroxide treatment in tolerant and susceptible wheat genotypes. Biol Plant 43:381–386

    Article  CAS  Google Scholar 

  • Schoffl F, Prandl R, Reindl A (1999) Regulation of the heat-shock response. Plant Physiol 117:1135–1137

    Article  Google Scholar 

  • Smith DF, Whitesell L, Nair SC, Chen S, Prapapanich V, Rimerman RA (1995) Progesterone receptor structure and function altered by geldanamycin, an hsp90-binding agent. Mol Cell Biol 15:6804–6812

    PubMed  CAS  Google Scholar 

  • Soliman WS, Fujimori M, Tase K, Sugiyama S (2011) Oxidative stress and physiological damage under prolonged heat stress in C3 grass Lolium perenne. Grassl Sci 57:101–106

    Article  CAS  Google Scholar 

  • Sung DY, Kaplan F, Lee KJ, Guy CL (2003) Acquired tolerance to temperature extremes. Trends Plant Sci 8:179–187

    Article  PubMed  CAS  Google Scholar 

  • Vierling E (1991) The roles of heat shock proteins in plants. Annu Rev Plant Physiol Plant Mol Biol 42:579–620

    Article  CAS  Google Scholar 

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Acknowledgments

The author sincerely thanks Indian Agricultural Research Institute (IARI) and Indian Council of Agriculture Research (ICAR) for financial assistance under National Initiative for Climate Resilient Agriculture (NICRA) project in order to take up the research work.

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Correspondence to Ranjeet R. Kumar.

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Kumar, R.R., Goswami, S., Sharma, S.K. et al. Differential expression of heat shock protein and alteration in osmolyte accumulation under heat stress in wheat. J. Plant Biochem. Biotechnol. 22, 16–26 (2013). https://doi.org/10.1007/s13562-012-0106-5

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