首页 | 本学科首页   官方微博 | 高级检索  
     检索      

猪肌生成抑制素(MSTN)基因cDNA克隆及序列分析
引用本文:乔宪凤,刘西梅,华文君,周荆荣,刘中华,张立萍,肖红卫,华再东,李莉,郑新民.猪肌生成抑制素(MSTN)基因cDNA克隆及序列分析[J].江西农业学报,2010,22(10).
作者姓名:乔宪凤  刘西梅  华文君  周荆荣  刘中华  张立萍  肖红卫  华再东  李莉  郑新民
摘    要:利用GenBank中猪肌生成抑制素(MSTN)编码序列设计引物,以湖北白猪背最长肌肌细胞总RNA为模板,利用RT-PCR技术,扩增出MSTN基因cDNA片段。该片段全长1277bp,包含猪MSTN基因的全部编码序列。将所得片段与pUCm-T载体连接,转化到DH5α大肠杆菌中,成功地筛选到阳性克隆,其质粒测序结果与文献报道的一致。

关 键 词:湖北白猪  肌生成抑制素  基因  克隆

Cloning and Sequencing of Hubei White Swine Myostatin Gene cDNA
QIAO Xian-feng,LIU Xi-mei,HUA Wen-jun,ZHOU Jing-rong,LIU Zhong-hua,ZHANG Li-ping,XIAO Hong-wei,HUA Zai-dong,LI Li,ZHENG Xin-min.Cloning and Sequencing of Hubei White Swine Myostatin Gene cDNA[J].Acta Agriculturae Jiangxi,2010,22(10).
Authors:QIAO Xian-feng  LIU Xi-mei  HUA Wen-jun  ZHOU Jing-rong  LIU Zhong-hua  ZHANG Li-ping  XIAO Hong-wei  HUA Zai-dong  LI Li  ZHENG Xin-min
Abstract:Total RNA of muscle cell was prepared from a pig breed Hubei white swine and was used to amplify myostatin(MSTN) gene cDNA by RT-PCR.The resulted cDNA fragment with the expected size was cloned into vector pUCm-T and identified by digestion with restrictive enzyme before being sequenced.The result showed that the cloned MSTN gene was 1277 bp in total length and comprised the complete coding sequence which was 99.5% homogenous to the reported swine MSTN genes with 3 nucleotides replacement and only one amino acid difference.
Keywords:Hubei white swine  Myostatin  Gene  Cloning
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号