Requirement for PCNA in DNA mismatch repair at a step preceding DNA resynthesis

被引:501
作者
Umar, A [1 ]
Buermeyer, AB [1 ]
Simon, JA [1 ]
Thomas, DC [1 ]
Clark, AB [1 ]
Liskay, RM [1 ]
Kunkel, TA [1 ]
机构
[1] OREGON HLTH SCI UNIV,DEPT MOL & MED GENET,PORTLAND,OR 97201
关键词
D O I
10.1016/S0092-8674(00)81323-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A two-hybrid system was used to screen yeast and human expression libraries for proteins that interact with mismatch repair proteins. PCNA was recovered from both libraries and shown in the case of yeast to interact with both MLH1 and MSH2. A yeast strain containing a mutation in the PCNA gene had a strongly elevated mutation rate in a dinucleotide repeat, and the rate was not further elevated in a strain also containing a mutation in MLH1. Mismatch repair activity was examined in human cell extracts using an assay that does not require DNA repair synthesis. Activity was inhibited by p21WAF1 or a p21 peptide, both of which bind to PCNA, and activity was restored to inhibited reactions by addition of PCNA. The data suggest a PCNA requirement in mismatch repair at a step preceding DNA resynthesis. The ability of PCNA to bind to MLH1 and MSH2 may reflect linkage between mismatch repair and replication and may be relevant to the roles of mismatch repair proteins in other DNA transactions.
引用
收藏
页码:65 / 73
页数:9
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