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西门塔尔牛肌肉生成抑制素基因编码序列的克隆与序列分析
引用本文:吕文发,赵静,袁天祥.西门塔尔牛肌肉生成抑制素基因编码序列的克隆与序列分析[J].中国牛业科学,2006,33(1):19-20,23.
作者姓名:吕文发  赵静  袁天祥
作者单位:吉林农业大学,动物科技学院,吉林,长春,130118
摘    要:本研究根据Genbank中牛肌肉生成抑制素基因序列设计引物,在设计的引物两端分别加上限制性内切酶BarnHI和EcoRI的识别位点序列。利用RT—PCR技术从西门塔尔牛肌肉组织的总RNA中扩增出MSTN基因的CDNA序列,扩增出1125bp片段,该片段与pMD18-T载体连接,转化JM109感受态细胞,所得阳性克隆进行酶切和PCR鉴定,并进行了测序分析,得到的克隆序列与设计的序列基本一致,表明成功地克隆了西门塔尔牛的肌肉生成抑制素基因的蛋白编码序列。

关 键 词:西门塔尔牛  肌肉生成抑制素  克隆
文章编号:1001-9111(2006)01-0019-02
收稿时间:2005-10-18
修稿时间:2005-10-18

Cloning and Analysis of Coding Sequence of Myostatin Gene in Simmental Cattle
LU Wen-fa,ZHAO Jing,YUANG Tian-xiang.Cloning and Analysis of Coding Sequence of Myostatin Gene in Simmental Cattle[J].China Cattle Science,2006,33(1):19-20,23.
Authors:LU Wen-fa  ZHAO Jing  YUANG Tian-xiang
Institution:College of Animal Science and Technology, Jilin Agricultural University, Changchun, Jilin 130008, China
Abstract:The primer added BamH I and EcoR I recognition site sequence were designed according to the cattle myostatin gene sequence in the Genbank.1 125 bp fragment of myostatin gene maturation region was amplified by RT-PCR from muscular tissue of Simmental cattle,and ligated with vector pMD18-T and transfecting JM109 competent cell.The sequence of identified positive clone by PCR and digested with restriction enzyme was analyzed,the same sequence between clone and designed sequence indicated that the myostatin gene of Simmental cattle was cloned successfully.
Keywords:Simrnental  Myostatin  Clone
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