PCNA Is Required for Initiation of Recombination-Associated DNA Synthesis by DNA Polymerase δ

被引:117
作者
Li, Xuan [1 ]
Stith, Carrie M. [3 ]
Burgers, Peter M. [3 ]
Heyer, Wolf-Dietrich [1 ,2 ]
机构
[1] Univ Calif Davis, Dept Microbiol, Davis, CA 95616 USA
[2] Univ Calif Davis, Dept Mol & Cellular Biol, Davis, CA 95616 USA
[3] Washington Univ, Dept Biochem & Mol Biophys, Sch Med, St Louis, MO 63110 USA
基金
美国国家卫生研究院;
关键词
CELL NUCLEAR ANTIGEN; HOMOLOGOUS RECOMBINATION; RAD54; PROTEIN; ESCHERICHIA-COLI; GENE CONVERSION; D-LOOPS; YEAST; REPAIR; STRAND; REPLICATION;
D O I
10.1016/j.molcel.2009.09.036
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Genetic recombination ensures proper chromosome segregation during meiosis and is essential for genome stability and tumor suppression. DNA synthesis after Rad51-mediated DNA strand invasion is a crucial step during recombination. PCNA is known as the processivity clamp for DNA polymerases. Here, we report the surprising observation that PCNA is specifically required to initiate recombination-associated DNA synthesis in the extension of the 3' end of the invading strand in a D loop. We show using a reconstituted system of yeast Rad51, Rad54, RPA, PCNA, RFC, and DNA polymerase delta that loading of PCNA by RFC targets DNA polymerase delta to the D loop formed by Rad51 protein, allowing efficient utilization of the invading 3' end and processive DNA synthesis. We conclude that PCNA has a specific role in the initiation of recombination-associated DNA synthesis and that DNA polymerase delta promotes recombination-associated DNA synthesis.
引用
收藏
页码:704 / 713
页数:10
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