Hasan A M Mahedi, Leach David R F
Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF United Kingdom.
Institute of Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF United Kingdom
Proc Natl Acad Sci U S A. 2015 Jul 28;112(30):9388-93. doi: 10.1073/pnas.1505370112. Epub 2015 Jul 13.
Defects in DNA mismatch repair (MMR) result in elevated mutagenesis and in cancer predisposition. This disease burden arises because MMR is required to correct errors made in the copying of DNA. MMR is bidirectional at the level of DNA strand polarity as it operates equally well in the 5' to 3' and the 3' to 5' directions. However, the directionality of MMR with respect to the chromosome, which comprises parental DNA strands of opposite polarity, has been unknown. Here, we show that MMR in Escherichia coli is unidirectional with respect to the chromosome. Our data demonstrate that, following the recognition of a 3-bp insertion-deletion loop mismatch, the MMR machinery searches for the first hemimethylated GATC site located on its origin-distal side, toward the replication fork, and that resection then proceeds back toward the mismatch and away from the replication fork. This study provides support for a tight coupling between MMR and DNA replication.
DNA错配修复(MMR)缺陷会导致突变率升高和癌症易感性增加。这种疾病负担的产生是因为需要MMR来纠正DNA复制过程中出现的错误。在DNA链极性层面,MMR是双向的,因为它在5'到3'和3'到5'方向上的运作效果相同。然而,MMR相对于由极性相反的亲本DNA链组成的染色体的方向性一直未知。在此,我们表明大肠杆菌中的MMR相对于染色体是单向的。我们的数据表明,在识别出一个3碱基对的插入-缺失环错配后,MMR机制会在其远离起始点的一侧朝着复制叉寻找第一个半甲基化的GATC位点,然后切除过程会朝着错配方向并远离复制叉进行。这项研究为MMR与DNA复制之间的紧密耦合提供了支持。