Liang Rubing, Liu Xipeng, Liu Jianhua, Ren Qiushi, Liang Peiji, Lin Zhixin, Xie Xiangming
College of Life Science and Technology, Shanghai Jiaotong University, 800 Dong-Chuan Road, Shanghai 200240, China.
J Microbiol Methods. 2007 Mar;68(3):497-506. doi: 10.1016/j.mimet.2006.10.016. Epub 2006 Dec 13.
Temperature-sensitive (TS) mutants of a gene are ones of which the activity or phenotype is very similar to that of wild type only at certain temperature and they provide extremely powerful tool for studying protein function in vivo. Here we report a novel strategy to generate TS phenotype of the interest gene in Escherichia coli based on a temperature-sensitive T7-expression system. A TS T7-RNA polymerase is generated by interrupting it with a TS intein from Saccharomyces cerevisiae vacuolar ATPase subunit (VMA), resulting that the gene flanked by T7-promoter and T7-terminator will be transcribed only at the permissive temperature (18 degrees C), not at the restrictive temperature (37 degrees C). The feasibility to create TS phenotype of this strategy was detected using lacZ as target. Reverse transcriptase polymerase chain reaction (PCR) indicated that at 18 degrees C, transcripts of T7-promoter controlled lacZ were at least 85 times more than those at 37 degrees C. Western blot analysis and enzymatic assay showed that large amounts of active His6-tagged LacZ produced at 18 degrees C but little at 37 degrees C. This strategy appears more promising than other TS creation methods because the target is pre-designed, no modification is introduced, and only simple DNA manipulation is required.
一个基因的温度敏感(TS)突变体是指其活性或表型仅在特定温度下与野生型非常相似的突变体,它们为在体内研究蛋白质功能提供了极其强大的工具。在此,我们报告一种基于温度敏感T7表达系统在大肠杆菌中产生感兴趣基因TS表型的新策略。通过用来自酿酒酵母液泡ATP酶亚基(VMA)的温度敏感内含肽中断T7-RNA聚合酶,产生一个TS T7-RNA聚合酶,结果是位于T7启动子和T7终止子两侧的基因仅在允许温度(18℃)下转录,而不在限制温度(37℃)下转录。以lacZ为靶标检测了该策略产生TS表型的可行性。逆转录聚合酶链反应(PCR)表明,在18℃时,T7启动子控制的lacZ转录本至少比在37℃时多85倍。蛋白质免疫印迹分析和酶活性测定表明,大量有活性的His6标签LacZ在18℃时产生,而在37℃时很少产生。该策略似乎比其他产生TS的方法更有前景,因为靶标是预先设计的,不引入修饰,只需要简单的DNA操作。