Genschel Jochen, Modrich Paul
Department of Biochemistry, Duke University Medical Center, Durham, North Carolina, USA.
Methods Enzymol. 2006;408:273-84. doi: 10.1016/S0076-6879(06)08017-7.
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.
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。