Crouse Gray F
Department of Biology, Emory University, Atlanta, GA 30322, USA.
DNA Repair (Amst). 2016 Feb;38:102-109. doi: 10.1016/j.dnarep.2015.11.020. Epub 2015 Dec 2.
At the heart of the mismatch repair (MMR) system are proteins that recognize mismatches in DNA. Such mismatches can be mispairs involving normal or damaged bases or insertion/deletion loops due to strand misalignment. When such mispairs are generated during replication or recombination, MMR will direct removal of an incorrectly paired base or block recombination between nonidentical sequences. However, when mispairs are recognized outside the context of replication, proper strand discrimination between old and new DNA is lost, and MMR can act randomly and mutagenically on mispaired DNA. Such non-canonical actions of MMR are important in somatic hypermutation and class switch recombination, expansion of triplet repeats, and potentially in mutations arising in nondividing cells. MMR involvement in damage recognition and signaling is complex, with the end result likely dependent on the amount of DNA damage in a cell.
错配修复(MMR)系统的核心是识别DNA错配的蛋白质。此类错配可以是涉及正常或受损碱基的错配,也可以是由于链错配导致的插入/缺失环。当此类错配在复制或重组过程中产生时,MMR将指导去除配对错误的碱基或阻止非同源序列之间的重组。然而,当在复制背景之外识别出错配时,新旧DNA之间的正确链区分就会丧失,MMR会对错配的DNA随机起作用并产生诱变作用。MMR的这种非典型作用在体细胞超突变和类别转换重组、三联体重复序列的扩增以及可能在非分裂细胞中产生的突变中很重要。MMR参与损伤识别和信号传导很复杂,最终结果可能取决于细胞中DNA损伤的量。