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湖羊MyoG基因CDS的克隆及其真核表达载体的构建
引用本文:许峰,秦玉蓉,阴彦辉,张振韬,宋正海,范广习,高波,李碧春.湖羊MyoG基因CDS的克隆及其真核表达载体的构建[J].中国畜牧杂志,2011,47(9).
作者姓名:许峰  秦玉蓉  阴彦辉  张振韬  宋正海  范广习  高波  李碧春
作者单位:1. 扬州大学动物科学与技术学院,江苏扬州,225009
2. 苏州市吴中区东山动物防疫站,江苏苏州,215128
基金项目:国家转基因重大专项(2008ZX08008-003、2009ZX08008-003B)
摘    要:参阅GenBank发表的波尔山羊肌细胞生成素(MyoG)基因序列,设计3对具有互补末端的特异性引物,分别扩增出湖羊MyoG基因的3个外显子,利用重叠PCR技术,将此3个外显子连接,并构建成重组质粒pcDNA3.0-MyoG,转染NIH-3T3细胞,RT-PCR鉴定。结果表明:成功克隆了湖羊MyoG基因的CDS,在离体细胞中MyoG基因发生了转录,这为进一步研究MyoG基因的体内外表达及生物学的活性奠定了基础。

关 键 词:MyoG基因  重叠PCR  真核表达载体  湖羊

Cloning Based on Overlapping PCR and Construction of Eukaryotic Expression Vector of MyoG Gene of Hu Sheep
XU Feng,QIN Yu-rong,YIN Yan-hui,ZHANG Zhen-tao,SONG Zheng-hai,FAN Guang-xi,GAO Bo,LI Bi-chun.Cloning Based on Overlapping PCR and Construction of Eukaryotic Expression Vector of MyoG Gene of Hu Sheep[J].Chinese Journal of Animal Science,2011,47(9).
Authors:XU Feng  QIN Yu-rong  YIN Yan-hui  ZHANG Zhen-tao  SONG Zheng-hai  FAN Guang-xi  GAO Bo  LI Bi-chun
Institution:XU Feng1,QIN Yu-rong1,YIN Yan-hui1,ZHANG Zhen-tao1,SONG Zheng-hai2,FAN Guang-xi2,GAO Bo1,LI Bi-chun1(1.College of Animal Science and Technology,Yangzhou University,Jiangsu Yangzhou 225009,2.Dongshan Animal Epidemic Prevention Station of Wuzhong District,Jiangsu Suzhou,215128)
Abstract:Three exons of myogenin(MyoG)gene of Hu Sheep were amplified using three pairs of primers designed according to the MyoG gene sequence of Boer goat in GenBank,then linked by overlapping PCR,and inserted into the eukaryotic expression vector pcDNA3.0.NIH-3T3 cell was transfected with the constructed recombinant plasmid pcDNA3.0-MyoG,the expression of MyoG was detected by RT-PCR.The results showed that CDS of MyoG was successfully cloned in Hu sheep.Enzyme,PCR,RT-PCR analysis indicated that the recombinant pl...
Keywords:MyoG gene  overlapping PCR  eukaryotic expression vector  Hu Sheep  
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