首页 | 本学科首页   官方微博 | 高级检索  
     

小鼠白血病抑制因子真核表达载体的构建及测序分析
引用本文:杨娜娜,朱靖,孟春花,杜立新. 小鼠白血病抑制因子真核表达载体的构建及测序分析[J]. 家畜生态, 2006, 0(1)
作者姓名:杨娜娜  朱靖  孟春花  杜立新
作者单位:泰山医学院基础医学研究所 山东泰安271000(杨娜娜),山东农业大学动物科技学院 山东泰安271018(朱靖,孟春花),中国农科院畜牧研究所 北京100094(杜立新)
基金项目:山东省自然科学基金项目(Z99D03)
摘    要:运用RT-PCR技术,克隆含信号肽和不含信号肽的小鼠分泌型白血病抑制因子cDNA,通过pMD18-T simple载体和pBS-T载体过渡,分别构建了真核表达载体pSecTag-mlif(sp )和pSecTag-mlif(sp-),酶切进行初步鉴定。利用Blast程序,搜索NCBI GeneBank中与构建表达载体中编码MLIF cDNA的同源序列,除在编码区216bp处碱基为G和在318bp处由G突变为T外,编码LIF基因的其余序列与已发表的完全一致。运用DNAMAN软件对翻译水平进行预测,结果发现这一突变位点并不影响蛋白的翻译。

关 键 词:白血病抑制因子  真核表达载体  胚胎干细胞

Construction of Eukaryotic Expression Vector of Mouse LIF cDNA and Sequence Analysis of Mouse LIF
Yang Na-na,Zhu Jing,Meng Chun-hua,Du Li-xin. Construction of Eukaryotic Expression Vector of Mouse LIF cDNA and Sequence Analysis of Mouse LIF[J]. Ecology of Domestic Animal, 2006, 0(1)
Authors:Yang Na-na  Zhu Jing  Meng Chun-hua  Du Li-xin
Affiliation:Yang Na-na~1,Zhu Jing~2,Meng Chun-hua~2,Du Li-xin~
Abstract:Mouse secreted LIF cDNA with and without signal peptide were cloned from mouse livers by RT-PCR,and then subcloned into pBS-T vector and pMD18-T simple vector.Digesting fragments were recovered and inserted into pSecTag/Hygro with molecular cloning technique.Restrictive enzymes digestion analysis and DNA sequence results revealed that the LIF gene was cloned into eukaryotic expression vector pSecTag/Hygro successfully.The expression vectors which were constructed were called pSecTag-mlif(sp~ ) and pSecTag-mlif(sp~-).The sequence encoding mouse LIF gene which were cloned is consistent with published sequence in GeneBank except that the encoding sequence had two mutations in 216bp and in 318bp.Using DNAMAN software,we found that the two mutations did not affect protein translation.
Keywords:Leukemia Inhibitory Factor  Eukaryotic expression vector  ES cell
本文献已被 CNKI 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