Expression of a Solanum sogarandinum SK3-type dehydrin enhances cold tolerance in transgenic cucumber seedlings

Plant Science

Volumn 170, Issue 6, 2006, Pages 1164-1172

  Yin, Zhimin ^a   Rorat, Tadeusz ^a   Szabala, Bartosz M ^a   Ziółkowska, Agnieszka ^b   Malepszy, Stefan ^b  

^a INSTITUTE OF PLANT GENETICS   (Poland)

^b WARSAW UNIVERSITY OF LIFE SCIENCES   (Poland)

Author keywords

Cold; Cucumis sativus L.; Dehydrin; Transgenic plants

Indexed keywords

ELECTROLYTES; PROTEINS; SEED;

COLD; CUCUMIS SATIVUS L.; DEHYDRIN; TRANSGENIC PLANTS;

GENES;

ELECTROLYTES; GENES; PROTEINS; SEEDLINGS;

CUCUMIS SATIVUS; SOLANUM; SOLANUM SOGARANDINUM;

EID: 33748255935     PISSN: 01689452     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.plantsci.2006.02.002     Document Type: Article

References (45)

1. Close T.J. Dehydrins: a commonalty in the response of plants to dehydration and low temperature. Physiol. Plant. 100 (1997) 291-296
2. Svensson J., Ismail A.M., Palva E.T., and Close T.J. Dehydrins. In: Storey K.B., and Storey J.M. (Eds). Sensing, Signalling and Cell Adaptation (2002), Elsevier, Amsterdam 155-171
3. Campbell S.A., and Close T.J. Dehydrins: genes, proteins, and associations with phenotypic traits. New Phytol. 137 (1997) 61-74
4. Egerton-Warburton L.M., Balsamo R.A., and Close T.J. Temporal accumulation and ultrastructural localization of dehydrins in Zea mays L. Physiol. Plant. 101 (1997) 545-555
5. Danyluk J., Perron A., Houde M., Limin A., Fowler B., Benhamou N., and Sarhan F. Accumulation of an acidic dehydrin in the vicinity of the plasma membrane during cold acclimation of wheat. Plant Cell 10 (1998) 623-638
6. Alsheikh M.K., Heyen B.J., and Randall S.K. Ion binding properties of the dehydrin ERD14 are dependent upon phosphorylation. J. Biol. Chem. 278 (2003) 40882-40889
7. Nylander M., Svensson J., Palva E.T., and Welin B.V. Stress-induced accumulation and tissue-specific localization of dehydrins in Arabidopsis thaliana. Plant Mol. Biol. 45 (2001) 263-279
8. Ismail A.M., Hall A.E., and Close T.J. Purification and partial characterization of a dehydrin involved in chilling tolerance during seedling emergence of cowpea. Plant Physiol. 120 (1999) 237-244
9. Kru{combining double acute accent}ger C., Berkowitz O., Stephan U.W., and Hell R. A metal-binding member of the late embryogenesis abundant protein family transports iron in the phloem of Ricinus communis L. J. Biol. Chem. 277 (2002) 25062-25069
10. Palva E.T., and Heino P. Molecular mechanism of plant cold acclimation and freezing tolerance. In: Li P., and Chen T. (Eds). Plant Cold Hardiness: Molecular Biology, Biochemistry and Physiology (1998), Plenum Press, New York 3-14
11. Hara M., Terashima S., Fukaya T., and Kuboi T. Enhancement of cold tolerance and inhibition of lipid peroxidation by citrus dehydrin in transgenic tabacco. Planta 217 (2003) 290-298
12. Hara M., Fujinaga M., and Kuboi T. Radical scavenging activity and oxidative modification of Citrus dehydrin. Plant Physiol. Biochem. 42 (2004) 657-662
13. Heyen B.J., Alsheikh M.K., Smith E.A., Torvik C.F., Seals D.F., and Randall S.K. The calcium-binding activity of a vacuole-associated, dehydrin-like protein is regulated by phosphorylation. Plant Physiol. 130 (2002) 675-687
14. Mohapatra S.S., Wolfraim L., Poole R.J., and Dhindsa R.S. Molecular cloning and relation to freezing tolerance of cold-acclimation-specific genes of alfalfa. Plant Physiol. 89 (1989) 375-380
15. Robertson A.J., Weninger A., Wilen R.W., Fu P., and Gusta L.V. Comparison of dehydrin gene expression and freezing tolerance in Bromus inermis and Secale cereale grown in controlled environments, hydroponics and the field. Plant Physiol. 106 (1994) 1213-1216
16. Zhu B., Choi D.W., Fenton R., and Close T.J. Expression of the barley dehydrin multigene family and the development of freezing tolerance. Mol. Gen. Genet. 264 (2000) 145-153
17. Welling A., Rinne P., Viherä-Aarnio A., Kontunen-Soppela S., Heino P., and Palva E.T. Photoperiod and temperature differentially regulate the expression of two dehydrin genes during overwintering of birch (Betula pubescens Ehrh.). J. Exp. Bot. 55 (2004) 507-516
18. Close T.J. Dehydrins: emergence of a biochemical role of a family of plant dehydration proteins. Physiol. Plant. 97 (1996) 795-803
19. Hara M., Wakasugi Y., Ikoma Y., Yano M., Ogawa K., and Kuboi T. cDNA sequence and expression of a cold-responsive gene in Citrus unshiu. Biosci. Biotechnol. Biochem. 63 (1999) 433-437
20. Sanchez-Ballesta M.T., Rodrigo M.J., Lafuente M.T., Granell A., and Zacarias L. Dehydrin from citrus, which confers in vitro dehydration and freezing protection activity, is constitutive and highly expressed in the flavedo of fruit but responsive to cold and water stress in leaves. J. Agric. Food Chem. 52 (2004) 1950-1957
21. Ismail A.M., Hall A.E., and Close T.J. Allelic variation of a dehydrin gene cosegregates with chilling tolerance during seedling emergence. Proc. Natl. Acad. Sci. U.S.A. 96 (1999) 13566-13570
22. Porat R., Pavoncello D., Lurie S., and McCollum T.G. Identification of a grapefruit cDNA belonging to a unique class of citrus dehydrins and characterization of its expression patterns under temperature stress conditions. Physiol. Plant. 115 (2002) 598-603
23. Porat R., Pasentsis K., Rozentzvieg D., Gerasopoulos D., Falara V., Samach A., Lurie S., and Kanellis A.K. Isolation of a dehydrin cDNA from orange and grapefruit citrus fruit that is specifically induced by the combination of heat followed by chilling temperatures. Physiol. Plant. 120 (2004) 256-264
24. Arora R., Wisniewski M.E., and Scorza R. Cold acclimation in genetically related (sibling) deciduous and evergreen peach (Prunus persica [L.] Batsch). I. Seasonal changes in cold hardiness and polypeptides of bark and xylem tissues. Plant Physiol. 99 (1992) 1562-1568
25. Arora R., and Wisniewski M.E. Cold acclimation in genetically related (sibling) deciduous and evergreen peach (Prunus persica [L.] Batsch). II. A 60-kilodalton bark protein in cold-acclimated tissues of peach is heat stable and related to the dehydrin family of proteins. Plant Physiol. 105 (1994) 95-101
26. Artlip T.S., Callahan A.M., Bassett C.L., and Wisniewski M.E. Seasonal expression of a dehydrin gene in sibling deciduous and evergreen genotypes of peach (Prunus persica [L.] Batsch). Plant Mol. Biol. 33 (1997) 61-70
27. Rorat T., Grygorowicz W.J., Irzykowski W., and Rey P. Expression of KS-type dehydrins is primarily regulated by factors related to organ type and leaf developmental stage during vegetative growth. Planta 218 (2004) 878-885
28. Danyluk J., Houde M., Rassart E., and Sarhan F. Differential expression of a gene encoding an acidic dehydrin in chilling sensitive and freezing tolerant gramineae species. FEBS Lett. 344 (1994) 20-24
29. Houde M., Daniel C., Lachapelle M., Allard F., Laliberte S., and Sarhan F. Immunolocalization of freezing-tolerance-associated proteins in the cetoplasm and nucleoplasm of wheat crown tissues. Plant J. 8 (1995) 583-593
30. Puhakainen T., Hess M.W., Makela P., Svensson J., Heino P., and Palva E.T. Overexpression of multiple dehydrin genes enhances tolerances to freezing stress in Arabidopsis. Plant Mol. Biol. 54 (2004) 743-753
31. V. Lång, The role of ABA and ABA-induced gene expression in cold acclimation of Arabidopsis thaliana, Ph.D. Dissertation, Uppsala, Swedish University of Agricultural Siences, Uppsala Genetic Center, Sweden, 1993.
32. Kaye C., Neven L., Hofig A., Li Q.B., Haskell D., and Guy C. Characterization of a gene for spinach CAP160 and expression of two spinach cold-acclimation proteins in tobacco. Plant Physiol. 116 (1998) 1367-1377
33. Yin Z., Pawłowicz I., Bartoszewski G., Malinowski R., Malepszy S., and Rorat T. Transcriptional expression of a Solanum sogarandinum pGT{proportion}Dhn10 gene fusion in cucumber, and its correlation with chilling tolerance in transgenic seedlings. Cell. Mol. Biol. Lett. 9 (2004) 891-902
34. Pawłowicz I., Grygorowicz W.J., and Rorat T. DHN10 dehydrin is not expressed in transgenic Solanum species plants when the Dhn10 gene is fused to a glucosyl transferase promoter. Cell. Mol. Biol. Lett. 9 (2004) 947-961
35. Rorat T. Changes in gene expression in a wild potato (Solanum sogarandinum) during cold acclimation. Acta Physiol. Plant. 23 (2001) 117-126
36. Rorat T., Szabala B.M., Grygorowicz W.J., Wojtowicz B., Yin Z., and Rey P. Expression of SK(3)-type dehydrin in transporting organs is associated with cold acclimation in Solanum species. Planta January (2006) 1-17 (Epub ahead of print)
37. Korobczak A., Aksamit A., Łukaszewicz M., Lorenc K., Rorat T., and Szopa J. The potato glucosyltransferase gene promoter is environmentally regulated. Plant Sci. 168 (2005) 339-348
38. Szwacka M., Morawski M., and Burza W. Agrobacterium tumefaciens-mediated cucumber transformation with thaumatin II cDNA. Genet. Pol. 37A (1996) 126-129
39. Yin Z., Bartoszewski G., Szwacka M., and Malepszy S. Cucumber transformation methods-the review. Biotechnologia 1 (2005) 95-113
40. Murashige T., and Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue culture. Physiol. Plant. 15 (1962) 473-497
41. Dellaporta S.L., Wood J., and Hicks J.B. A plant DNA minipreparation: version II. Plant Mol. Biol. Rep. 1 (1983) 19-21
42. Rorat T., Sadowski J., Irzykowski W., Ziegler P., and Daussant J. Differential expression of two β-amylase genes of rye during seed development. Physiol. Plant. 94 (1995) 19-24
43. Rorat T., and Irzykowski W. Changes in mRNA population during cold acclimation in two potato lines of Solanum sogarandinum differing by their cold hardiness. Acta Physiol. Plant. 18 (1996) 25-32
44. Puhakainen T., Li C., Boije-Malm M., Kangajärvi J., Heino P., and Palva E.T. Short-day potentiation of low temperature-induced gene expression of a C-repeat-binding factor-controlled gene during cold acclimation in Silver birch. Plant Physiol. 136 (2004) 4299-4307
45. Lee S.C., Lee M.Y., Kim S.J., Jun S.H., An G., and Kim S.R. Characterization of an abiotic stress-inducible dehydrin gene, OsDhn1, in rice (Oryza sativus L.). Mol. Cells 19 (2005) 212-218