Rewinski C, Marinus M G
Department of Pharmacology, University of Massachusetts Medical School, Worcester 01655-2937.
Nucleic Acids Res. 1987 Oct 26;15(20):8205-15. doi: 10.1093/nar/15.20.8205.
The Dam-directed post-replicative mismatch repair system of Escherichia coli removes base pair mismatches from DNA. The products of the mutH, mutL and mutS genes, among others, are required for efficient mismatch repair. Absence of any of these gene products leads to persistence of mismatches in DNA with a resultant increase in spontaneous mutation rate. To determine the specificity of the mismatch repair system in vivo we have isolated and characterized 47 independent mutations from a mutH strain in the plasmid borne mnt repressor gene. The major class of mutations comprises AT to GC transitions that occur within six base pairs of the only two 5'-GATC-3' sequences in the mnt gene. In the wild type control strain, insertion of the IS1 element was the major spontaneous mutational event. A prediction of the Dam-directed mismatch repair model, that the mutation spectra of dam and mutH strains should be the same, was confirmed.
大肠杆菌的Dam介导的复制后错配修复系统可从DNA中去除碱基对错配。错配修复高效进行需要mutH、mutL和mutS等基因的产物。缺少这些基因产物中的任何一种都会导致DNA中的错配持续存在,从而导致自发突变率增加。为了确定体内错配修复系统的特异性,我们从携带mnt阻遏基因的质粒中的mutH菌株中分离并鉴定了47个独立突变。主要的突变类型包括mnt基因中仅有的两个5'-GATC-3'序列的六个碱基对内发生的AT到GC的转换。在野生型对照菌株中,IS1元件的插入是主要的自发突变事件。Dam介导的错配修复模型的一个预测,即dam和mutH菌株的突变谱应该相同,得到了证实。