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人类DNA错配修复中切除步骤的分析。

Analysis of the excision step in human DNA mismatch repair.

作者信息

Genschel Jochen, Modrich Paul

机构信息

Department of Biochemistry, Duke University Medical Center, Durham, North Carolina, USA.

出版信息

Methods Enzymol. 2006;408:273-84. doi: 10.1016/S0076-6879(06)08017-7.

Abstract

The reaction responsible for replication error correction by mismatch repair proceeds via several steps: mismatch recognition, mismatch-provoked excision, repair DNA synthesis, and ligation. Key steps in this process are the recognition and subsequent exonucleolytic removal of the mispair. A minimal system comprised of human MutSalpha (MSH2MSH6), MutLalpha (MLH1PMS2), exonuclease I (EXOI), replication protein A (RPA), proliferating cell nuclear antigen (PCNA), and replication factor C (RFC) is sufficient to support mismatch-provoked excision in vitro. This chapter describes methods for analysis of the reconstituted excision reaction.

摘要

错配修复负责复制错误校正的反应通过几个步骤进行

错配识别、错配引发的切除、修复性DNA合成和连接。该过程的关键步骤是错配的识别以及随后的核酸外切酶去除错配。一个由人类MutSα(MSH2MSH6)、MutLα(MLH1PMS2)、核酸外切酶I(EXOI)、复制蛋白A(RPA)、增殖细胞核抗原(PCNA)和复制因子C(RFC)组成的最小系统足以在体外支持错配引发的切除。本章描述了分析重组切除反应的方法。

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