hMSH3 and hMSH6 interact with PCNA and colocalize with it to replication foci

被引:194
作者
Kleczkowska, HE [1 ]
Marra, G [1 ]
Lettieri, T [1 ]
Jiricny, J [1 ]
机构
[1] Paul Scherrer Inst, CH-8008 Zurich, Switzerland
关键词
PCNA; hMSH6; hMSH3; mismatch repair; DNA repair; replication foci;
D O I
10.1101/gad.191201
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Proliferating cell nuclear antigen (PCNA) has been implicated in eukaryotic postreplicative mismatch correction, but the nature of its interaction with the repair machinery remained enigmatic. We now show that PCNA binds to the human mismatch binding factors hMutS alpha and hMutS beta via their hMSH6 and hMSH3 subunits, respectively. The N-terminal domains of both proteins contain the highly conserved PCNA-binding motif Qxx[LI]xx[FF]. A variant of hMutS alpha, lacking this motif because of deletion of 77 N-terminal residues of the hMSH6 subunit, no longer was able to interact with PCNA in vitro and failed to restore mismatch repair in hMSH6-deficient cells. Colocalization of PCNA and hMSH6 or hMSH3 to replication foci implies an intimate link between replication and mismatch correction. We postulate that PCNA plays a role in repair initiation by guiding the mismatch repair proteins to free termini in the newly replicated DNA strands.
引用
收藏
页码:724 / 736
页数:13
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