Suppr超能文献

解旋酶活性是否有助于真核生物中的错配修复?

Does a helicase activity help mismatch repair in eukaryotes?

机构信息

Department of Biochemistry and Molecular Biology, Miller School of Medicine, University of Miami, Miami, FL 33136, USA.

出版信息

IUBMB Life. 2010 Jul;62(7):548-53. doi: 10.1002/iub.349.

Abstract

Mismatch repair (MMR) corrects innate DNA replication infidelities. Many components of eukaryotic MMR have been identified, the molecular mechanism of MMR has been largely demonstrated, and furthermore the nick-directed MMR reactions have been reconstituted with purified human proteins in vitro. However, some fundamental questions still remain to be answered. One such question is whether a DNA helicase activity is required for MMR in eukaryotes. This short review presents an overview of the interactions between eukaryotic DNA helicases and MMR factors, and suggests a possible mechanism for how DNA helicases may be involved in repair of DNA mismatches.

摘要

错配修复(MMR)纠正先天的 DNA 复制错误。已经鉴定出真核生物 MMR 的许多组成部分,MMR 的分子机制在很大程度上已被证实,并且已经在体外使用纯化的人类蛋白重新构建了切口定向的 MMR 反应。然而,仍有一些基本问题有待解答。其中一个问题是在真核生物中是否需要 DNA 解旋酶活性来进行 MMR。这篇简短的综述概述了真核生物 DNA 解旋酶与 MMR 因子之间的相互作用,并提出了 DNA 解旋酶可能参与修复 DNA 错配的可能机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验