DNA damage tolerance

被引:63
作者
Branzei, Dana [1 ]
Psakhye, Ivan [1 ]
机构
[1] FIRC Inst Mol Oncol, IFOM, Via Adamello 16, I-20139 Milan, Italy
关键词
REPLICATION FORK REVERSAL; MUTATION-RATES; POSTREPLICATION REPAIR; CHROMATIN ORGANIZATION; CELLULAR-RESPONSE; PCNA RECRUITS; UBIQUITIN; PROTEIN; SUMO; PATHWAY;
D O I
10.1016/j.ceb.2016.03.015
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Accurate chromosomal DNA replication is fundamental for optimal cellular function and genome integrity. Replication perturbations activate DNA damage tolerance pathways, which are crucial to complete genome duplication as well as to prevent formation of deleterious double strand breaks. Cells use two general strategies to tolerate lesions: recombination to a homologous template, and trans-lesion synthesis with specialized polymerases. While key players of these processes have been outlined, much less is known on their choreography and regulation. Recent advances have uncovered principles by which DNA damage tolerance is regulated locally and temporally - in relation to replication timing and cell cycle stage -, and are beginning to elucidate the DNA dynamics that mediate lesion tolerance and influence chromosome structure during replication.
引用
收藏
页码:137 / 144
页数:8
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