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水稻中一个与OsHSP90互作的新基因特性分析

Characteristic Analysis on a Novel Gene Interacted with OsHSP90 from Rice
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摘要 OsHSP90是水稻中一类可以在不同逆境条件下被诱导的基因。利用酵母双杂交系统,在水稻低温和干旱cDNA文库中筛选出1个与OsHSP90互作的未知基因,命名为OsHSPBP。序列分析表明,该基因全长1321 bp,编码一个具有244个氨基酸残基的多肽,推测分子量为25.5 kD。在OsHSPBP蛋白的97-132位氨基酸残基间存在tify功能域,185-211位氨基酸残基构成CCT_2基序,与其他植物中的同源蛋白相似性介于30.66%-70.40%。经分析,该基因启动子区域存在6种不同的逆境反应顺式作用元件。RT-PCR半定量结果表明,OsHSP90与OsHSPBP在逆境胁迫下,均能被不同程度地诱导并呈现相似的表达趋势,说明两者可能与水稻逆境胁迫的应答和信号传递有关。 OsHSP90 is an abiotic stress-inducible gene in rice. From the chilling and drought-inducible cDNA library of rice, a novel gene, OsHSPBP, which interacted with OsHSPgO was identified by using yeast two-hybrid system. The 1321 bp full length cDNA of OsHSPBP was cloned. Its open reading frame (ORF) predicts a 244-amino acid(aa) polypeptide with calculated molecular weight of 25.5 kD. A tify motif and a CCT_2 motif were found at the aa 97-132 and aa 185--211, respectively. Sequence similarity analysis indicated that the OsHSPBP had 30.66 %- 70.40% identities with the tify family proteins from other plants. Among the putative promoter region, six factors matched to cis-elements related to the abiotic stress response were identified using the PlantCARE software. Semi-quantitative RT-PCR showed that the OsHSP90 and OsHSPBP might he detected in the similar degree under different stress-treatments, suggesting that OsHSP90 and OsHSPBP could be involved in the signal transmission and response to the abiotic stress in rice.
出处 《中国水稻科学》 CAS CSCD 北大核心 2009年第4期342-348,共7页 Chinese Journal of Rice Science
基金 教育部长江学者和创新团队发展计划资助项目(IRT0453) 国家科技支撑计划资助项目(2007BAD81B00)
关键词 水稻 逆境胁迫 诱导基因 基因表达 氨基酸序列 酵母双杂交系统 rice abiotic stressl inducible gene gene expressionl amino acid sequencel yeast two-hybrid system
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参考文献13

  • 1Kotak S,Larkindale J,Lee U,et al.Complexity of the heat stress response in plants.Curr Opin Plant Biol,2007,103:310-316.
  • 2Picard D.Heat-shock protein 90,a chaperone for folding and regulation.Cell & Mol Life Sci,2002,59(10):1640-1648.
  • 3Zimmerman J L,Petri W,Meselson M.Accumulation of specific subsets of D.melanogaster heat shock mRNAs in normal development without heat shock.Cell,1983,32(4):1161-1170.
  • 4Krishna P,Sacco M,Cherutti J F,et al.Cold-induced accumulation of HSP90 transcripts in Brassica napus.Plant Physiol,1995,107(3):915-923.
  • 5Marrs K A,Casey E S,Capitant S A,et al.Characterization of two maize HSP90 heat shock protein genes:Expression during heat shock,embryogenesis,and pollen development.Dev Genet,1993,14(1):27-41.
  • 6Schmitz G,Schmidt M,Feierabend J.Characterization of a plastid-specific HSP90 homologue:Identification of a cDNA sequence,phylogenetic descendence and analysis of its mRNA and protein expression.Plant Mol Biol,1996,30(3):479-492.
  • 7Zhao R,Davey M,Hsu Y C,et al.Navigating the chaperone network:An integrative map of physical and genetic interactions mediated by the HSP90 chaperone.Cell,2005,120(5):715-742.
  • 8Stebbins C E,Russo A A,Schneider C,et al.Crystal structure of an HSP90-geldanamycin complex:Targeting of a protein chaperone by an antitumor agent.Cell,1997,89(2):239-250.
  • 9Logemann J,Schell J,Willmitzer L.Improved method for the isolation of RNA from plant tissues.Anal Biochem,1987,163(1):16-20.
  • 10Wegele H,Muller L,Buchner J.HSP70 and HSP90:A relay team for protein folding.Rev Physiol Biochem Pharmacol,2004,151:1-44.

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