Lahue R S, Modrich P
Department of Biochemistry, Duke University Medical Center, Durham, NC 27710.
Mutat Res. 1988 Mar;198(1):37-43. doi: 10.1016/0027-5107(88)90037-1.
Some of the molecular aspects of methyl-directed mismatch repair in E. coli have been characterized. These include: mismatch recognition by mutS protein in which different mispairs are bound with different affinities; the direct involvement of d(GATC) sites; and strand scission by mutH protein at d(GATC) sequences with strand selection based on methylation of the DNA at those sites. In addition, communication over a distance between a mismatch and d(GATC) sites has been implicated. Analysis of mismatch correction in a defined system (Lahue et al., unpublished) should provide a direct means to further molecular aspects of this process.
大肠杆菌中甲基定向错配修复的一些分子层面已得到表征。这些包括:MutS蛋白识别错配,其中不同的错配以不同的亲和力结合;d(GATC)位点的直接参与;以及MutH蛋白在d(GATC)序列处进行链断裂,并根据这些位点处DNA的甲基化情况进行链选择。此外,错配与d(GATC)位点之间远距离的通信也有涉及。在一个明确的系统中对错配校正进行分析(拉胡等人,未发表)应能为进一步研究这一过程的分子层面提供直接手段。