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猪Follistatin cDNA克隆及在大肠杆菌中的表达
引用本文:何新,齐冰,何立千,陈永福,刘桂生,陈清轩.猪Follistatin cDNA克隆及在大肠杆菌中的表达[J].生物工程学报,2006,22(4):677-681.
作者姓名:何新  齐冰  何立千  陈永福  刘桂生  陈清轩
作者单位:1. 中国科学院遗传与发育生物学研究所,北京,100080;中国科学院研究生院,北京,100049
2. 北京联合大学师范学院应用生物技术系,北京,100083
3. 中国农业大学农业生物技术国家重点实验室,北京,100094
4. 中国科学院遗传与发育生物学研究所,北京,100080
基金项目:北京联合大学校科研和教改项目
摘    要:提取猪卵巢总RNA,用RT-PCR方法克隆了猪FollistatincDNA的完整开放阅读框,长1038bp。将FollistatincDNA连接到原核表达载体pGEX-4T-3中,转化大肠杆菌BL21(DE3),以IPTG诱导,进行了GST-FS融合蛋白表达。用SDS-PAGE和Western杂交检测,结果显示在63kD处有特异性表达蛋白。

关 键 词:RT-PCR  猪Follistatin  cDNA  原核表达
文章编号:1000-3061(2006)04-0677-05
修稿时间:2005年12月26

Porcine Follistatin cDNA Cloning and Expression in Escherichia coli
HE Xin,QI Bing,HE Li-Qian,CHEN Yong-Fu,LIU Gui-Sheng,CHEN Qing-Xuan.Porcine Follistatin cDNA Cloning and Expression in Escherichia coli[J].Chinese Journal of Biotechnology,2006,22(4):677-681.
Authors:HE Xin  QI Bing  HE Li-Qian  CHEN Yong-Fu  LIU Gui-Sheng  CHEN Qing-Xuan
Institution:Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100080, China.
Abstract:The total RNA was extracted from porcine ovary. Porcine Follistatin cDNA was cloned by RT-PCR. Complete porcine follistatin cDNA coding sequences are presented including 1038 bp of open reading frame. The purified porcine follistatin cDNA was inserted into pGEX-4T-3 vector to construct the prokaryotic fusion protein expression vector. The recombinant expression plasmid was transformed into BL21 (DE3) and expression was induced by IPTG. Protein products were detected by SDS-PAGE and confirmed by Western blotting analysis, which showed that the yield of the Follistatin cDNA was a 63kD protein expression vector. Follistatin protein was expressed in the form of glutathione-S-transferase (GST) fusion protein in E. coli.
Keywords:RT-PCR  porcine follistatin cDNA  prokaryotes expression  
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