MutS and MutL sliding clamps in DNA mismatch repair

Xiao-Peng Han , Xiao-Wen Yang , Jiaquan Liu

Genome Instability & Disease ›› 2022, Vol. 4 ›› Issue (1) : 1 -11.

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Genome Instability & Disease ›› 2022, Vol. 4 ›› Issue (1) : 1 -11. DOI: 10.1007/s42764-022-00094-x
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MutS and MutL sliding clamps in DNA mismatch repair

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Abstract

DNA mismatch repair (MMR) corrects mispair nucleotides that arise from polymerase misincorporation. Highly conserved MutS (MSH) and MutL (MLH/PMS) homologs initiate MMR, and in higher eukaryotes act as DNA damage sensors that can trigger apoptosis. The MSH proteins recognize the mismatch nucleotides, whereas the MLH/PMS proteins mediate multiple protein–protein interactions associated with downstream MMR events including strand-specific incision and excision. Remarkably, the mechanics of the MSH and MLH/PMS proteins have been elusive for decades. Here we summarize and discuss recent biophysical studies of core MMR components, especially focusing on the unique conformations of MSH and MLH/PMS proteins that lead to the coordination of multiple repair events.

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Xiao-Peng Han, Xiao-Wen Yang, Jiaquan Liu. MutS and MutL sliding clamps in DNA mismatch repair. Genome Instability & Disease, 2022, 4(1): 1-11 DOI:10.1007/s42764-022-00094-x

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National Natural Science Foundation of China(32071283)

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