应用与环境生物学报
應用與環境生物學報
응용여배경생물학보
CHINESE JOURNAL OF APPLIED & ENVIRONMENTAL BIOLOGY
2009年
1期
87-90
,共4页
金福厚%庞岩%李士泽%杨焕民%计红%赵巧香%尹位
金福厚%龐巖%李士澤%楊煥民%計紅%趙巧香%尹位
금복후%방암%리사택%양환민%계홍%조교향%윤위
冷诱导RNA结合蛋白%cDNA%克隆%冷应激%序列分析
冷誘導RNA結閤蛋白%cDNA%剋隆%冷應激%序列分析
랭유도RNA결합단백%cDNA%극륭%랭응격%서렬분석
CIRP%eDNA%cloning%cold stress%sequence analysis
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凶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,从其睾丸组织巾克隆出了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%、99.40%、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.图5参14
冷誘導RNA結閤蛋白(Cold inducible RNA-binding protein,CIRP)在多種冷應激細胞(包括重組中國倉鼠卵巢細胞)中被髮現.迄今為止,冷應激對活體生物基兇錶達的影響還未見報道.和細胞相比,生物體具有更加複雜的冷應激調節機製.本研究以冷處理的BALB/C鼠為實驗動物,從其睪汍組織巾剋隆齣瞭CIRP的cDNA.結果錶明,CIRP在生物體中能夠被低溫誘導,可能防止生物體遭受冷損傷.根據剋隆的cDNA所推測的氨基痠序列與GenBank上公佈的小鼠、大鼠、人類、牛蛙、美西螈、非洲爪蟾胚胎細胞和卵母細胞的CIRP氨基痠序列同源性分彆為100%、99.40%、95.5%、67.4%、58.4%、76.9%和79.1%.這錶明CIRP在生物進化過程中是高度保守的,可能具有多種生理功能.因此,這一研究將為探索人類和動物冷應激分子機製創立繫統試驗模型和奠定新的實踐基礎.圖5參14
랭유도RNA결합단백(Cold inducible RNA-binding protein,CIRP)재다충랭응격세포(포괄중조중국창서란소세포)중피발현.흘금위지,랭응격대활체생물기흉표체적영향환미견보도.화세포상비,생물체구유경가복잡적랭응격조절궤제.본연구이랭처리적BALB/C서위실험동물,종기고환조직건극륭출료CIRP적cDNA.결과표명,CIRP재생물체중능구피저온유도,가능방지생물체조수랭손상.근거극륭적cDNA소추측적안기산서렬여GenBank상공포적소서、대서、인류、우와、미서원、비주조섬배태세포화란모세포적CIRP안기산서렬동원성분별위100%、99.40%、95.5%、67.4%、58.4%、76.9%화79.1%.저표명CIRP재생물진화과정중시고도보수적,가능구유다충생리공능.인차,저일연구장위탐색인류화동물랭응격분자궤제창립계통시험모형화전정신적실천기출.도5삼14
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 cDNA 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