RAD18-mediated ubiquitination of PCNA activates the Fanconi anemia DNA repair network

被引:84
作者
Geng, Liyi [1 ]
Huntoon, Catherine J. [1 ]
Karnitz, Larry M. [1 ,2 ,3 ]
机构
[1] Mayo Clin, Coll Med, Div Oncol Res, Rochester, MN 55905 USA
[2] Mayo Clin, Coll Med, Dept Mol Pharmacol & Expt Therapeut, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Dept Radiat Oncol, Rochester, MN 55905 USA
关键词
CROSS-LINK REPAIR; CELL NUCLEAR ANTIGEN; DEFECTIVE POSTREPLICATION REPAIR; CORE COMPLEX; MAMMALIAN-CELLS; HOMOLOGOUS RECOMBINATION; TRANSLESION SYNTHESIS; HUMAN RAD18; DAMAGE; MONOUBIQUITINATION;
D O I
10.1083/jcb.201005101
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Fanconi anemia (FA) network is important for the repair of interstrand DNA cross-links. A key event in FA pathway activation is the monoubiquitylation of the FA complementation group I (FANCI)-FANCD2 (ID) complex by FA complementation group L (FANCL), an E3 ubiquitin ligase. In this study, we show that RAD18, another DNA damage-activated E3 ubiquitin ligase, also participates in ID complex activation by ubiquitylating proliferating cell nuclear antigen (PCNA) on Lysl 64, an event required for the recruitment of FANCL to chromatin. We also found that monoubiquitylated PCNA stimulates FANCL-catalyzed FANCD2 and FANCI monoubiquitylation. Collectively, these experiments identify RAD18-mediated PCNA monoubiquitination as a central hub for the mobilization of the FA pathway by promoting FANCL-mediated FANCD2 monoubiquitylation.
引用
收藏
页码:249 / 257
页数:9
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