Regulations of marker genes involved in biotic and abiotic stress by overexpression of the AtNDPK2 gene in rice

Biochemical and Biophysical Research Communications

Volumn 363, Issue 1, 2007, Pages 126-132

  Seong, Eun Soo ^a   Guo, Jia ^a   Kim, Young Hwa ^b   Cho, Joon Hyeong ^b   Lim, Chun Keun ^a   Hyun Hur, Jang ^a   Wang, Myeong Hyeon ^a  

^a Kangwon National University   (South Korea)

^b Dongguk University   (South Korea)

Author keywords

AtNDPK2; Chilling stress; Co transformation; Oxidative stress; Pathogen related proteins

Indexed keywords

ATNDPK2 PROTEIN; GENE PRODUCT; HYDROGEN PEROXIDE; OSAPX1 PROTEIN; OSAPX2 PROTEIN; OSPR2 PROTEIN; OSPR4 PROTEIN; OSSODB PROTEIN; OXYGEN RADICAL; PBC442 PROTEIN; PBC601 PROTEIN; SUPEROXIDE; UNCLASSIFIED DRUG;

ABIOTIC STRESS; ARTICLE; BIOTIC STRESS; CONTROLLED STUDY; GENE CONTROL; GENE OVEREXPRESSION; GENETIC TRANSCRIPTION; GROWTH RETARDATION; MARKER GENE; NONHUMAN; NUCLEOTIDE SEQUENCE; OXIDATIVE STRESS; PATHOGENESIS; PLANT GROWTH; PRIORITY JOURNAL; RICE; TRANSGENIC CROP;

ARABIDOPSIS PROTEINS; GENE EXPRESSION REGULATION, PLANT; GENETIC MARKERS; NUCLEOSIDE-DIPHOSPHATE KINASE; ORYZA SATIVA; OXIDATIVE STRESS; REACTIVE OXYGEN SPECIES; RECOMBINANT PROTEINS; UP-REGULATION;

EID: 34548800234     PISSN: 0006291X     EISSN: 10902104     Source Type: Journal    
DOI: 10.1016/j.bbrc.2007.08.147     Document Type: Article

References (46)

1. Cushman J.C., and Bohnert H.J. Genomic approaches to plant stress tolerance. Curr. Opin. Plant Biol. 3 (2000) 117-124
2. Yamaguchi-Shinozaki K., and Shinozaki K. Organization of cis-acting regulatory elements in osmotic-and cold-stress-responsive promoters. Trends Plant Sci. 10 (2005) 88-94
3. Umezawa T., Fujita M., Fujita Y., Yamaguchi-Shinozaki K., and Shinozaki K. Engineering drought tolerance in plants: discovering and tailoring genes to unlock the future. Curr. Opin. Plant Biotech. 17 (2006) 113-122
4. Timmusk S., and Wagner E.G. The plant-growth-promoting Rhizobacterium paenibacillus polymyxa induces changes in Arabidopsis thaliana gene expression: a possible connection between biotic and abiotic stress responses. Mol. Plant Microbe Interact. 12 (1999) 951-959
5. Buchanan C.D., Lim S., Salzman R.A., Kagiampakis I., Morishige D.T., Weers B.D., Klein R.R., Pratt L.H., Cordonnier-Pratt M.M., Klein P.E., and Mullet J.E. Sorghum bicolor's transcriptome response to dehydration, high salinity and ABA. Plant Mol. Biol. 58 (2005) 687-698
6. Davies K.J. Oxidative stress: the paradox of aerobic life. Biochem. Soc. Symp. 61 (1995) 1-31
7. Halliwell B., and Gutteridge J.M.C. Free Radicals in Biology and Medicine (1999), Oxford University Press, Oxford, NY
8. Zelko I.N., Mariani T.J., and Folz R.J. Superoxide dismutase multigene family: a comparison of the CuZn-SOD (SOD1), Mn-SOD (SOD2), and EC-SOD (SOD3) gene structures, evolution, and expression. Free Radic. Biol. Med. 33 (2002) 337-349
9. Hasegawa P.M., Bressan R.A., Zhu J.K., and Bohnert H.J. Plant cellular and molecular responses to high salinity. Annu. Rev. Plant Physiol. Plant Mol. Biol. 51 (2000) 463-499
10. Valliyodan B., and Nguyen H.T. Understanding regulatory networks and engineering for enhanced drought tolerance in plants. Curr. Opin. Plant Biotech. 9 (2006) 189-195
11. Otero A.S. NM23/nucleoside diphosphate kinase and signal transduction. J. Bioenerg. Biomembr. 32 (2000) 269-275
12. Cipollini G., Berti A., Fiore L., Rainaldi G., Basolo F., Bevilacqua G., and Caligo M.A. Down regulation of nm23 H1 gene inhibits cell proliferation. Int. J. Cancer 73 (1997) 297-302
13. Engel M., Seifert M., Theisinger B., Seyfert U., and Welter C. Glyceraldehyde-3-phosphate dehydrogenase and Nm23-H1/nucleoside diphosphate kinase A. Two old enzymes combine for the novel Nm23 protein phosphotransferase function. J. Biol. Chem. 273 (1998) 20058-20065
14. Wagner P.D., and Vu N.D. Histidine to aspartate phosphotransferase activity of nm23 proteins: phosphorylation of aldolase C on Asp-319. Biochem. J. 346 (2000) 623-630
15. Choi G., Yi H., Lee J., Kwon Y.K., Soh M.S., Shin B., Luka Z., Hahn T.R., and Song P.S. Phytochrome signalling is mediated through nucleoside diphosphate kinase 2. Nature 401 (1999) 610-613
16. Galvis M.L., Marttila S., Hakansson G., Forsberg J., and Knorpp C. Heat stress response in pea involves interaction of mitochondrial nucleoside diphosphate kinase with a novel 86-kilodalton protein. Plant Physiol. 126 (2001) 69-77
17. Zimmermann S., Baumann A., Jaekel K., Marbach I., Engelberg D., and Frohnmeyer H. UV-responsive genes of Arabidopsis revealed by similarity to the Gcn4-mediated UV response in yeast. J. Biol. Chem. 274 (1999) 17017-17024
18. Pan L., Kawai M., Yano A., and Uchimiya H. Nucleoside diphosphate kinase required for coleoptile elongation in rice. Plant Physiol. 122 (2000) 447-452
19. Shen Y., Kim J.I., and Song P.S. NDPK2 as a signal transducer in the phytochrome-mediated light signaling. J. Biol. Chem. 280 (2005) 5740-5749
20. Moon H.J., Lee B.Y., Choi G., Shin D.J., Theertha Prasad D., Lee O.S., Kwak S.S., Kim D.H., Nam J.S., Bahk J.D., Hong J.C., Lee S.Y., Cho M.J., Lim C.O., and Yun D.J. NDPkinase 2 interacts with two oxidative stress activated MAPKs to regulate cellular redox state and enhances multiple stress tolerance in transgenic plants. Proc. Natl. Acad. Sci. USA 100 (2003) 358-363
21. Ignacimuthu S., Arockiasamy S., and Terada R. Genetic transformation of rice: current status and future prospects. Curr. Sci. 79 (2000) 186-195
22. Zhang J., Feng Q., Jin C., Qiu D., Zhang L., Xie K., Yuan D., Han B., Zhang Q., and Wang S. Features of the expressed sequences revealed by a large-scale analysis of ESTs from a normalized cDNA library of the elite indica rice cultivar Minghui 63. Plant J. 42 (2005) 772-780
23. Kim K.Y., Kwon S.Y., Bang J.W.D., and Kwak S.S. A novel oxidative stress-inducible peroxidase promoter from sweetpotato: molecular cloning and characterization in transgenic sweetpotato plants and cell cultured cells. Plant Mol. Biol. 51 (2003) 831-838
24. An G. Binary Ti vectors for plant transformation and promoter analysis. Methods Enzymol. 153 (1987) 292-305
25. Hiei Y., Ohta S., Komari T., and Kumashiro T. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J. 6 (1994) 271-282
26. Yi S.Y., Kim J.H., Joung Y.H., Lee S., Kim W.T., Yu S.H., and Choi D. The pepper transcription factor CaPF1 confers pathogen and freezing tolerance in Arabidopsis. Plant Physiol. 136 (2004) 2862-2874
27. Komari T., Hiei Y., Saito Y., and Murai N. Vectors carrying two separate T-DNAs for co-transformation of higher plants mediated by Agrobacterium tumefaciens and segregation of transformants free from selection markers. Plant J. 10 (1996) 165-174
28. Depicker A., Herman L., Jacobs A., Schell J., and Montagu M.V. Frequencies of simultaneous transformation with different TDNAs and their relevance to the Agrobacterium/plant cell interaction. Mol. Gen. Genet. 201 (1985) 477-484
29. Petit A., Berkaloff A., and Tempe J. Multiple transformation of plant cells by Agrobacterium may be responsible for the complex organization of T-DNA in crown gall and hairy root. Mol. Gen. Genet. 202 (1985) 388-393
30. McKnight T.D., Lillis M.T., and Simpson R.B. Segregation of genes transferred to one plant cell from two separate Agrobacterium strains. Plant Mol. Biol. 8 (1987) 439-445
31. Framond A.J.D., Back E.W., Chilton W.S., Kayes L., and Chilton M. Two unlinked T-DNAs can transform the same tobacco plant cell and segregate in the F1 generation. Mol. Gen. Genet. 202 (1986) 125-131
32. Park J., Lee Y.K., Kang B.K., and Chung W.I. Co-transformation using a negative selectable marker gene for the production of selectable marker gene-free transgenic plants. Theor. Appl. Genet. 109 (2004) 1562-1567
33. Kim H.J., Kim Y.K., Park J.Y., and Kim J. Mutation in domain II of IAA1 confers diverse auxin-related phenotypes and represses auxin-activated expression of Aux/IAA genes in steroid regulator-inducible system. Plant J. 29 (2002) 693-704
34. Guy C.L. Cold acclimation and freezing stress tolerance: role of protein metabolism. Ann. Rev. Plant Physiol. Plant Mol. Biol. 41 (1990) 187-223
35. Tran Binh L., and Oono K. Ecotypical responses and specific protein pattern of rice seedlings and callus during chilling treatment. Jpn. J. Breed. 39 (1989) 132-133
36. Kasamo K. Response of tonoplast and membrane ATPases in chilling-sensitive and -insensitive rice (Oryza sativa L.) culture cells to low temperature. Plant Cell Physiol. 29 (1988) 1085-1094
37. Jeong S.W., Choi S.M., Lee D.S., Ahn S.N., Hur Y., Chow W.S., and Park Y.I. Differential susceptibility of photosynthesis to light-chilling stress in rice (Oryza sativa L.) depends on the capacity for photochemical dissipation of light. Mol. Cell 13 (2002) 419-428
38. Cheng C., Yun K.Y., Ressom H.W., Mohanty B., Bajic V.B., Jia Y., Yun S.J., and de los Reyes B.G. An early response regulatory cluster induced by low temperature and hydrogen peroxide in seedlings of chilling-tolerant japonica rice. BMC Genomics 8 (2007) 175
39. Tran Binh L., and Oono K. Molecular cloning and characterization of genes related to chilling tolerance in rice. Plant Physiol. 99 (1992) 1146-1150
40. Bowler C., Van Montagu M., and Inzé D. Superoxide dismutase and stress tolerance. Annu. Rev. Plant Physiol. Plant Mo1. Biol. 43 (1992) 83-116
41. Perl-Treves R., and Galun E. The tomato Cu,Zn superoxide dismutase genes are developmentally regulated and respond to light and stress. Plant Mo1. Biol. 17 (1991) 745-760
42. Sakamoto A., Okumura T., Kaminaka H., and Tanaka K. Molecular cloning of the gene (SodCc7) that encodes a cytosolic copper/zinc-superoxide dismutase from rice (Oryza sativa L.). Plant Physiol. 107 (1995) 651-652
43. Shigeoka S., Ishikawa T., Tamoi M., Miyagawa Y., Takeda T., Yabuta Y., and Yoshimura K. Regulation and function of ascorbate peroxidase isoenzymes. J. Exp. Bot. 53 (2002) 1305-1319
44. Agrawala G.K., Jwac N.S., Iwahashid H., and Rakwalb R. Importance of ascorbate peroxidases OsAPX1 and OsAPX2 in the rice pathogen response pathways and growth and reproduction revealed by their transcriptional profiling. Gene 322 (2003) 93-103
45. Agrawal G.K., Jwa N.S., Han K.S., Agrawal V.P., and Rakwal R. Isolation of a novel rice PR4 type gene whose mRNA expression is modulated by blast pathogen attack and signaling components. Plant Physiol. Biochem. 41 (2003) 81-90
46. Um M.O., Park T.I., Kim Y.J., Seo H.Y., Kim J.G., Kwon S.Y., Kwak S.S., Yun D.J., and Yun S.J. Particle bombardment-mediated transformation of barley with an Arabidopsis NDPK2 cDNA. Plant Biotechnol. Rep. 1 (2007) 71-77