Lieb M, Rehmat S
Department of Microbiology, University of Southern California School of Medicine, Los Angeles 90033.
J Bacteriol. 1995 Feb;177(3):660-6. doi: 10.1128/jb.177.3.660-666.1995.
In Escherichia coli, T:G mismatches in specific contexts are corrected by a very short patch (VSP) repair system. Previous studies have shown that the product of gene vsr mediates correction of T:G to C:G in the 5'CTAGG/3'GGTCC context and in some related contexts. Amber mutations that arose in CAG sequences in gene cI of bacteriophage lambda were used to determine the effect of flanking bases on the repair of T:G mispairs arising during phage recombination. The experimental findings were combined with published data on mismatch repair of mutations in lambda gene P and E. coli gene lacI. While VSP repair was most efficient in the context 5'CTAGG, there was very significant correction when either the 5'C or the 3' G was replaced by another base. Some mismatch repair of TAG to CAG occurred in all contexts tested. Reduction in VSP repair caused by the lack of MutL or MutS was fully complemented by the addition of vsr+ plasmids when the T:G mispair was in the 5'CTAGG/3'GGTCC context. VSP repair was decreased in bacteria containing mutS+ on a multicopy plasmid. It is suggested that VSP repair maintains sequences such as the repetitive extragenic palindromic (REP) and Chi sequences, which have important roles in E. coli and closely related bacteria.
在大肠杆菌中,特定环境下的T:G错配可由一个极短片段(VSP)修复系统进行校正。先前的研究表明,基因vsr的产物介导了在5'CTAGG/3'GGTCC环境及一些相关环境中T:G到C:G的校正。利用噬菌体λ基因cI中CAG序列出现的琥珀突变来确定侧翼碱基对噬菌体重组过程中产生的T:G错配修复的影响。实验结果与已发表的关于λ基因P和大肠杆菌基因lacI中突变错配修复的数据相结合。虽然VSP修复在5'CTAGG环境中效率最高,但当5'C或3'G被另一个碱基取代时,也有非常显著的校正。在所有测试环境中都发生了一些TAG到CAG的错配修复。当T:G错配处于5'CTAGG/3'GGTCC环境时,添加vsr + 质粒可完全弥补因缺乏MutL或MutS而导致的VSP修复减少。在多拷贝质粒上含有mutS + 的细菌中,VSP修复减少。有人提出,VSP修复维持了诸如重复基因外回文序列(REP)和Chi序列等序列,这些序列在大肠杆菌及密切相关细菌中具有重要作用。