Parker B O, Marinus M G
Department of Pharmacology, University of Massachusetts Medical School, Worcester 01655.
Proc Natl Acad Sci U S A. 1992 Mar 1;89(5):1730-4. doi: 10.1073/pnas.89.5.1730.
Plasmid heteroduplexes were constructed that contain 1, 2, 3, 4, or 5 unpaired bases within the mnt gene. These were used to assess the efficiency of repair of small heterologous sequences ("heterologies") in DNA by the Escherichia coli Dam-directed mismatch repair system. Heteroduplexes in defined states of methylation at d(GATC) sites were used to transform a repair-proficient indicator strain (which has a mnt-lac fusion coding for a nonfunctional mnt repressor) and its isogenic mutH, -L, and -S derivatives. Using this in vivo transformation system, we scored for repair on the basis of colony color: correction in favor of the strand bearing mnt+ coding information gives rise to colonies that are white, whereas correction on the opposite strand (mnt-) yields colonies that are red when grown on MacConkey agar. Failure to repair a heterology yields colonies that are both red and white ("mixed"). The correction efficiencies of two heteroduplexes, each containing a single G.T mismatch within mnt, were also monitored for purposes of comparison. Our results show that mutHLS-dependent, methyl-directed repair of heteroduplexes with 1-, 2-, and 3-base deletions is as highly efficient as the repair of G.T mismatches. Heteroduplexes with a 4-base deletion are marginally repaired and DNA with a 5-base deletion is not detectably repaired. In addition, we show that purified MutS protein from Salmonella typhimurium, which can substitute for E. coli MutS in vivo, binds to oligonucleotide duplexes containing 1, 2, 3, and 4 unpaired bases of a sequence identical with that used for the in vivo studies. Specific binding of MutS to homoduplex DNA and to DNA that had undergone a 5-base deletion was not observed.
构建了在mnt基因内含有1、2、3、4或5个未配对碱基的质粒异源双链体。这些用于评估大肠杆菌Dam定向错配修复系统对DNA中小的异源序列(“异源部分”)的修复效率。在d(GATC)位点处于特定甲基化状态的异源双链体用于转化一个具有修复能力的指示菌株(其具有编码无功能mnt阻遏物的mnt - lac融合基因)及其同基因的mutH、-L和-S衍生物。利用这个体内转化系统,我们根据菌落颜色对修复情况进行评分:偏向携带mnt +编码信息的链的校正会产生白色菌落,而在相反链(mnt -)上的校正会在麦康凯琼脂上生长时产生红色菌落。未能修复异源部分会产生红色和白色菌落(“混合”)。为了进行比较,还监测了两个异源双链体的校正效率,每个异源双链体在mnt内都含有一个单一的G.T错配。我们的结果表明,对于具有1个、2个和3个碱基缺失的异源双链体,依赖mutHLS的甲基定向修复与G.T错配的修复效率一样高。具有4个碱基缺失的异源双链体仅得到少量修复,而具有5个碱基缺失的DNA未检测到修复。此外,我们表明,来自鼠伤寒沙门氏菌的纯化的MutS蛋白,其在体内可替代大肠杆菌的MutS,能与含有与体内研究中所用序列相同的1、2、3和4个未配对碱基的寡核苷酸双链体结合。未观察到MutS与同源双链DNA以及经历了5个碱基缺失的DNA的特异性结合。