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作 者:金福厚[1] 庞岩 李士泽[1] 杨焕民[1] 计红[1] 赵巧香[1] 尹位[1]
机构地区:[1]黑龙江八一农垦大学动物科技学院,大庆163319 [2]黑龙江强尔生化技术开发有限公司,哈尔滨150090
出 处:《应用与环境生物学报》2009年第1期87-90,共4页Chinese Journal of Applied and Environmental Biology
基 金:Supported by the National Postdoctoral Science Foundation of China (GrantNo. 20060390241);the Postdoctoral Science Foundation of Heilongjiang,China
摘 要:冷诱导RNA结合蛋白(Cold inducible RNA-binding protein,CIRP)在多种冷应激细胞(包括重组中国仓鼠卵巢细胞)中被发现.迄今为止,冷应激对活体生物基因表达的影响还未见报道.和细胞相比,生物体具有更加复杂的冷应激调节机制.本研究以冷处理的BALB/C鼠为实验动物,从其睾丸组织中克隆出了CIRP的cDNA.结果表明,CIRP在生物体中能够被低温诱导,可能防止生物体遭受冷损伤.根据克隆的cDNA所推测的氨基酸序列与GenBank上公布的小鼠、大鼠、人类、牛蛙、美西螈、非洲爪蟾胚胎细胞和卵母细胞的CIRP氨基酸序列同源性分别为100%、99.4%、95.5%、67.4%、58.4%、76.9%和79.1%.这表明CIRP在生物进化过程中是高度保守的,可能具有多种生理功能.因此,这一研究将为探索人类和动物冷应激分子机制创立系统试验模型和奠定新的实践基础.The cold-inducible RNA-binding protein (CIRP) was found in various cells including recombinant Chinese hamster ovary (rCHO) cells under cold stress. However, the effect of cold stress on the gene expression of the intravital animals has not been reported till now. Compared with their cells, there were much more complicated regulatory mechanisms for cold stress response in the organisms. The BALB/C mice with cold treatment were used as experimental animals for this study. The cDNA of CIRP was firstly cloned from the testis tissues of the BALB/C mice treated by cold stress. The results indicated that CIRP in the organisms could be induced at low temperature and might protect the organisms from the cold damage. The amino acid sequences deduced via eDNA clone were 100%, 99.4%, 95.5%, 67.4%, 58.4%,76.9%, and 79.1% identical to those of the CIRP in mice, rats, human, bullfrog and axolotl cells, and Xenopus embryos and oocytes, respectively. These results show that the CIRP is highly conserved in the evolution process and may be involved in various physiological functions. Therefore, this study will establish a systematic model for experiments and provide a new foundation for exploring the molecular mechanisms of human and animals under cold stress. Fig 5, Ref 14
关 键 词:冷诱导RNA结合蛋白 CDNA 克隆 冷应激 序列分析
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