Erianthus arundinaceus HSP70 (EaHSP70) overexpression increases drought and salinity tolerance in sugarcane (Saccharum spp. hybrid)

Plant Science

Volumn 232, Issue , 2015, Pages 23-34

  Augustine, Sruthy Maria ^a   Narayan, J Ashwin ^a   Syamaladevi, Divya P ^b   Appunu, C ^a   Chakravarthi, M ^a   Ravichandran, V ^c   Subramonian, N ^a  

^a SUGARCANE BREEDING INSTITUTE   (India)

^b INDIAN GRASSLAND AND FODDER RESEARCH INSTITUTE   (India)

^c TAMIL NADU AGRICULTURAL UNIVERSITY   (India)

Author keywords

Drought tolerance; Erianthus arundinaceus; HSP70; Salinity tolerance; Sugarcane; Transformation

Indexed keywords

ERIANTHUS ARUNDINACEUS; SACCHARUM;

HEAT SHOCK PROTEIN 70; WATER;

DROUGHT; GENETICS; METABOLISM; PHYSIOLOGY; SALT TOLERANCE; SUGARCANE; TRANSGENIC PLANT;

DROUGHTS; HSP70 HEAT-SHOCK PROTEINS; PLANTS, GENETICALLY MODIFIED; SACCHARUM; SALT-TOLERANCE; WATER;

EID: 84920276154     PISSN: 01689452     EISSN: 18732259     Source Type: Journal    
DOI: 10.1016/j.plantsci.2014.12.012     Document Type: Article

References (62)

1. Augustine S.M., Syamaladevi D.P., Premachandran M.N., Ravichandran R., Subramonian N. Physiological and molecular insights to drought responsiveness in Erianthus spp. Sugar Tech 2014, 10.1007/s12355-014-0312-7.
2. Amalraj V.A., Rakkiyappan P., Neelamathi D., Chinnaraj S., Subramanian S. Wild cane as a renewable source for fuel and fibre in the paper industry. Curr. Sci. 2008, 95(11):1599-1602.
3. Vierling E. The roles of heat shock proteins in plants. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1991, 42:579-620.
4. Trent J.D. A review of acquired thermotolerance, heat-shock proteins and molecular chaperones in Archaea. FEMS Microbiol. Rev. 1996, 18:249-258.
5. Boorstein W.R., Ziegelhoffer T., Craig E.A. Molecular evolution of the HSP70 multigene family. J. Mol. Evol. 1994, 38:1-17.
6. Evans C.G., Lyra C., Jason E.G. Heat shock protein 70 (Hsp70) as an emerging drug target. J. Med. Chem. 2010, 53(12):4585-4602.
7. Cho E.K., Hong C.B. Over-expression of tobacco NtHSP 70-1 contributes to drought stress tolerance in plants. Plant Cell Rep. 2006, 25:349-358.
8. Cho E.K., Choi Y.J. A nuclear-localized HSP70 confers thermo protective activity and drought-stress tolerance on plants. Biotechnol. Lett. 2009, 31:597-606.
9. Ono K. Overexpression of DnaK from a halotolerant cyanobacterium Aphanothece halophytica enhances the high temperature tolerance of tobacco during germination and early growth. Plant Sci. 2001, 160:455-461.
10. Qi Y., Wang H., Zou Y., Liu C., Liu Y., Wang Y., Zhang W. Over-expression of mitochondrial heat shock protein 70 suppresses programmed cell death in rice. FEBS Lett. 2011, 585:231-239.
11. Uchida A., Hibino A., Shimada T., Saigusa M., Takabe T., Araki E., Kajita H., Takabe T. Overexpression of DnaK chaperone from a halotolerant cyanobacterium Aphanothece halophytica increases seed yield in rice and tobacco. Plant Biotechnol. 2008, 25:141-150.
12. Montero-Barrientos M. Transgenic expression of the Trichoderma harzianum hsp70 gene increases Arabidopsis resistance to heat and other abiotic stresses. J. Plant Physiol. 2010, 167:659-665.
13. Song A., Zhu X., Chen F., Gao H., Jiang J., Chen S. A Chrysanthemum heat shock protein confers tolerance to abiotic stress. Int. J. Mol. Sci. 2014, 15:5063-5078.
14. Phillip A., Syamaladevi D.P., Chakravarthy M., Gopinath K., Subramonian N. 5' Regulatory region of ubiquitin 2 gene from Porteresia coarctata makes efficient promoters for transgene expression in monocots and dicots. Plant Cell Rep. 2013, 32:1199-1210.
15. Sambrook J., Russel D.W. Molecular Cloning: A Laboratory Manual 1989, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY. third ed.
16. Arvinth S., Arun S., Selvakesavan R.K., Srikanth J., Mukunthan N., Ananda Kumar P., Premachandran M.N., Subramonian N. Genetic transformation and pyramiding of aprotinin expressing sugarcane with cry1Ab for shoot borer (Chilo infuscatellus) resistance. Plant Cell Rep. 2010, 29:383-395.
17. Bettina M.J.E., Melvin T.T., Thomas A.K. Visual assessment of wilting as a measure of leaf water potential and seedling drought survival. J. Trop. Ecol. 2007, 23:497-500.
18. Martineau J.R., Specht J.E., Williams J.H., Sullivan C.Y. Temperature tolerance in soybeans. I. Evaluation of a technique for assessing cellular membrane thermostability. Crop Sci. 1979, 19:75-78.
19. Molaei P., Namvar A.E.A., Bejandi T.K. Water relation, solute accumulation and cell membrane injury in sesame (Sesamum indicum L.) cultivars subjected to water stress. Ann. Biol. Res. 2012, 3(4):1833-1838.
20. Barrs H.D., Weatherley P.E. A reexamination of the relative turgidity technique for estimating water deficits in leaves. Aust. J. Biol. Sci. 1962, 15:413-428.
21. Chomczynski P., Mackey K. Modification of the TRI reagent DNA/protein isolation procedure for isolation of RNA from polysaccharide and proteoglycan rich sources. Biotechniques 1995, 19:942-945.
22. Basu S., Roychoudhury A. Expression profiling of abiotic stress inducible genes in response to multiple stresses in rice (Oryza sativa L.) varieties with contrasting level of stress tolerance. Biol. Med. Res. Int. 2014, 2014. ID-706890.
23. Cheng M., Liao P., Lin T. The Arabidopsis ethylene responsive factor 1 regulates abiotic stress responsive gene expression by binding to different cis-acting elements in response to different stress signals. Plant Physiol. 2013, 162(3):1566-1582.
24. -δCT method. Methods 2001, 25:402-408.
25. Fan L., Zheng S., Wang X. Antisense suppression of phospholipase Da retards abscisic acid and ethylene-promoted senescence of postharvest Arabidopsis leaves. Plant Cell 1997, 9:2183-2196.
26. Crafts-Brandner S.J., Below F.E., Harper J.E., Hageman R.H. Effects of pod removal on metabolism and senescence of nodulating and nonnodulating Soybean isolines: II. Enzymes and chlorophyll. Plant Physiol. 1984, 75(2):318-322.
27. Cornejo M.J., Luth D., Blankenship K.M., Anderson O.D., Blechl A.E. Activity of a maize ubiquitin promoter in transgenic rice. Plant Mol. Biol. 1993, 13:567-581.
28. Takimoto I., Christensen A.H., Quail P.H., Uchimiya H., Toki S. Non-systemic expression of a stress-responsive maize polyubiquitin gene (Ubi-1) in transgenic rice plants. Plant Mol. Biol. 1994, 26:1007-1012.
29. Garbarino J.E., Oosumi T., Belknap W.R. Isolation of a polyubiquitin promoter and its expression in transgenic potato plants. Plant Physiol. 1995, 109(4):1371-1378.
30. Ahn Y.J., Zimmerman J.L. Introduction of the carrot HSP17.7 into potato (Solanum tuberosum L.) enhances cellular membrane stability and tuberization in vitro. Plant Cell Environ. 2006, 29:95-104.
31. Camejo D., Rodri{dotless}guez P., Morales M.A., Dellamico J.M., Torrecillas A., Alarcon J.J. High temperature effects on photosynthetic activity of two tomato cultivars with different heat susceptibility. J. Plant Physiol. 2005, 162:281-289.
32. Momcilovic I., Ristic Z. Expression of chloroplast protein synthesis elongation factor, EF-Tu, in two lines of maize with contrasting tolerance to heat stress during early stages of plant development. J. Plant Physiol. 2007, 164:90-99.
33. Gunasekera D., Berkowitz G.A. Evaluation of contrasting cellular-level acclimation responses to leaf water deficits in three wheat genotypes. Plant Sci. 1992, 86:1-12.
34. Ritchie S.W., Nguyan H.T., Holaday A.S. Leaf water content and gas-exchange parameters of two wheat genotypes differing in drought resistance. Crop Sci. 1990, 30:105-111.
35. Alizade A. Soil, Water and Plants Relationship 2002, Emam Reza University Press, Mashhad, Iran, ISBN: 964-6582-21-4 (in Persian). third ed.
36. El Jaafari S. Durum wheat breeding for abiotic stresses resistance: defining physiological traits and criteria. Options Mediterr. Ser. A 2000, 40:251-256.
37. Kramer P.J., Boyer J.S. Water Relations of Plants and Soils 1995, 495. Academic Press, San Diego.
38. Wright G.C., Nageswara R., Farquhar G.D. Water use efficiency and carbon isotope discrimination in peanut under water deficit conditions. Crop Sci. 1994, 34:92-97.
39. Nageswara Rao R.C., Talwar H.S., Wright G.C. Rapid assessment of specific leaf area and leaf nitrogen in peanut (Arachis hypogaea L.) using a chlorophyll meter. J. Agron. Crop Sci. 2001, 186:175-182.
40. Van der Mescht A., de Ronde J.A., Rossouw F.T. Chlorophyll fluorescence and chlorophyll content as a measure of drought tolerance in potato. S. Afr. J. Sci. 1999, 95:407-412.
41. Angelopoulos K., Dichio B., Xiloyannis C. Inhibition of photosynthesis in olive trees (Olea europaea L.) during water stress and rewatering. J. Exp. Bot. 1996, 47:1093-1100.
42. Baker N.R., Bowyer J. Photoinhibition of Photosynthesis: From Molecular Mechanisms to Field 1994, BOIS Scientific Publishers Ltd., Oxford, UK.
43. Long S.P., Humphries S., Falkowski P.G. Photoinhibition of photosynthesis in nature. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1994, 45:633-662.
44. Khan M.S. The role of DREB transcription factors in abiotic stress tolerance of plants. Biotechnol. Biotechnol. Equip. 2011, 25(3):2433-2442.
45. Mizoi J., Shinozaki K., Yamaguchi-Shinozaki K. AP2/ERF family transcription factors in plant abiotic stress responses. Biochim. Biophys. Acta 2011, 1819(2):86-96.
46. Qin H., Qiang G., Junling Z., Li Sun Sundaram K., Yizheng Z., Mark B., Paxton P., Eduardo B., Hong Z. Regulated expression of an isopentenyl transferase gene (IPT) in peanut significantly improves drought tolerance and increases yield under field conditions. Plant Cell Physiol. 2011, 52(11):1904-1914.
47. Wang W., Vinocur B., Shoseyov O., Altman A. Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response. Trends Plant Sci. 2004, 9:244-252.
48. Frydman J. Folding of newly translated proteins in vivo: the role of molecular chaperones. Annu. Rev. Biochem. 2001, 70:603-647.
49. Miernyk J.A. The 70kDa stress-related proteins as molecular chaperones. Trends Plant Sci. 1997, 2:80-87.
50. Sung D.Y., Vierling E., Guy C.L. Comprehensive expression profile analysis of the Arabidopsis hsp70 gene family. Plant Physiol. 2001, 126:789-800.
51. Lee J.H., Schoffl F. An Hsp70 antisense gene affects the expression of HSP70/HSC70, the regulation of HSF and the acquisition of thermotolerance in transgenic Arabidopsis thaliana. Mol. Gen. Genet. 1996, 252:11-19.
52. Ding X.Z., Tsokos G.C., Kiang J.G. Overexpression of HSP-70 inhibits the phosphorylation of HSF1 by activating protein phosphatase and inhibiting protein kinase C activity. FASEB J. 1998, 12:451-459.
53. Galau G.A., Hughes D.W. Coordinate accumulation of homologous transcripts of seven cotton LEA gene families during embryogenesis and germination. Dev. Biol. 1987, 123:213-221.
54. Tunnacliffe A., Wise M.J. The continuing conundrum of the LEA proteins. Naturwissenschaften 2007, 94:791-812.
55. Dure L., Crouch M., Harada J., Ho T.H.D., Mundy J., Quatrano R. Common amino acid sequence domains among the LEA proteins of higher plants. Plant Mol. Biol. 1989, 12:475-486.
56. Nakashima K., Kiyosue T., Yamaguchi-Shinozaki K., Shinozaki K. A nuclear gene, erd1, encoding a chloroplast-targeted Clp protease regulatory subunit homolog is not only induced by water stress but also developmentally upregulated during senescence in Arabidopsis thaliana. Plant J. 1997, 12:851-861.
57. Shinozaki K., Yamaguchi-Shinozaki K. Molecular responses to dehydration and low temperature: differences and cross talk between two stress-signaling pathways. Curr. Opin. Plant Biol. 2000, 3:217-223.
58. Riechmann J.L., Heard J., Martin G., Reuber L., Jiang C., Keddie J., Adam L., Pineda O., Ratcliffe O.J., Samaha R.R., Creelman R., Pilgrim M., Broun P., Zhang J.Z., Ghandehari D., Sherman B.K., Yu G. Arabidopsis transcription factors: genome-wide comparative analysis among eukaryotes. Science 2000, 290(5499):2105-2110.
59. Jaglo-Ottosen K.R., Gilmour S.J., Zarka D.G., Schabenberger O., Thomashow M.F. Arabidopsis CBF1 overexpression induces COR genes and enhances freezing tolerance. Science 1998, 280:104-106.
60. Frank M.J., Cartwright H.N., Smith L.G. Three brick genes have distinct functions in a common pathway promoting polarized cell division and cell morphogenesis in the maize leaf epidermis. Development 2002, 130:753-762.
61. Amudha J., Balasubramani G. Recent molecular advances to combat abiotic stress tolerance in crop plants. Biotechnol. Mol. Biol. Rev. 2010, 6(2):31-58.
62. Guo S., Wharton W., Moseley P., Shi H. Heat shock protein 70 regulates cellular redox status by modulating glutathione related enzyme activities. Cell Stress Chaperones 2007, 12(3):245-254.