›› 2009, Vol. 36 ›› Issue (1): 38-40.

• 生物技术 • 上一篇    下一篇

猪IκBα基因定点突变中两种方法的应用

李和刚1,2,傅田1,靳二辉1,操继跃2,李奎1,肖邦1,杨述林1
  

  1. 1.中国农业科学院北京畜牧兽医研究所,中国农业科学院家养动物遗传资源与种质创新重点开放实验室, 北京 100193; 2.华中农业大学动物医学院, 武汉 430070
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2009-01-20 发布日期:2009-01-20

Application of Two Methods for Sitespecific Mutagenesis of Porcine IκBα

LI He-gang1,2,FU Tian1,JIN Er-hui1,CAO Ji-yue2,LI Kui1,XIAO Bang1,YANG Shu-lin1   

  1. 1.Key Laboratory of Domestic Animal Genetic Resources and Germplasm Innovation of CAAS, Institute of Animal Sciences(IAS),Chinese Acadamy of Agricultural Sciences(CAAS),Beijing 100193,China; 2.School of Veterinary Medicine, Huazhong Agricultural University,Wuhan 430070,China
  • Received:1900-01-01 Revised:1900-01-01 Online:2009-01-20 Published:2009-01-20

摘要: 作者将猪IκBα基因32、36位丝氨酸位点突变为丙氨酸,为进一步研究突变型IκBα蛋白对异种移植延缓性排斥反应的抑制机理奠定基础。首先采用Stratagene公司单点突变试剂盒将猪IκBα基因32位丝氨酸位点突变为丙氨酸,接着试图在36位引入突变但未成功,最后改用重叠延伸PCR对36位进行突变。结果表明,两种突变方法结合使用,成功地将猪IκBα基因32、36位丝氨酸位点突变为丙氨酸。说明两种突变方法各有所长,又有各自的缺点,应根据试验的实际需要灵活选择合适的突变方法,以收到事半功倍的效果。

关键词: 定点突变; 重叠延伸PCR; 猪IκBα基因

Abstract: Substitute Ala for the sites of Ser 32 and Ser 36 in porcine IκBα gene,to establish the fundament for mechanism research of the mutant IκBα inhibition on delayed xenograft rejection.QuikChange SiteDirected Mutagenesis Kit was first uesd for the mutagenesis of Ser 32 site,then the kit was subsequently used for the mutagenesis of Ser 36 site,but failed. Finally OEPCR was used for the mutagenesis of Ser 36 site. These two mutagenesis methods were combined to achieve sitespecific mutagenesis at the sites of 〖JP2〗Ser 32 and Ser 36 in porcine IκBα gene.These two methods each has a unique,and each has their own shortcoming.So,in order to get better result by less work,mutation methods should be chosen flexibly according to the real need.

Key words: sitespecific mutagenesis; OEPCR; porcine IκBα

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