DNA错配修复的分子机制

Peggy Hsieh
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引用次数: 199

摘要

DNA错配修复(MMR)保护了基因组的完整性。在复制后修复中,这种修复途径纠正了碱基和插入/删除(I/D)错配,这些错配逃脱了复制聚合酶的校对功能。在缺乏它的情况下,细胞呈现突变表型,其中自发突变率大大提高。错配修复缺陷与某些癌症易感性综合征分离的发现突出了其在突变避免中的重要作用。最近,识别错配的关键修复蛋白MutS的三维结构已经通过x射线晶体学确定。本文概述了MutS蛋白的结构特征,并讨论了结构数据如何与生化和遗传学研究一起揭示错配修复的分子机制。
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Molecular mechanisms of DNA mismatch repair

DNA mismatch repair (MMR) safeguards the integrity of the genome. In its role in postreplicative repair, this repair pathway corrects base–base and insertion/deletion (I/D) mismatches that have escaped the proofreading function of replicative polymerases. In its absence, cells assume a mutator phenotype in which the rate of spontaneous mutation is greatly elevated. The discovery that defects in mismatch repair segregate with certain cancer predisposition syndromes highlights its essential role in mutation avoidance. Recently, three-dimensional structures of MutS, a key repair protein that recognizes mismatches, have been determined by X-ray crystallography. This article provides an overview of the structural features of MutS proteins and discusses how the structural data together with biochemical and genetic studies reveal new insights into the molecular mechanisms of mismatch repair.

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