The multifaceted functions of homologous recombination in dealing with replication-associated DNA damages

被引:10
作者
Chakraborty, Shrena [1 ,2 ,3 ]
Schirmeisen, Kamila [1 ,2 ,3 ]
Lambert, Sarah A. E. [1 ,2 ,3 ,4 ]
机构
[1] Univ PSL, Inst Curie, CNRS UMR3348, F-91400 Orsay, France
[2] Univ Paris Saclay, CNRS UMR3348, F-91400 Orsay, France
[3] Equipe Labelisee Ligue Natl Canc, Orsay, France
[4] Univ PSL, Univ Paris Saclay, Inst Curie, CNRS UMR3348, F-91400 Orsay, France
关键词
Homologous recombination; Replication stress; Fork integrity and restart; Post-replicative gap repair; Cancer; Genome instability; BREAK-INDUCED REPLICATION; FORK REVERSAL; REPAIR; RAD51; STRESS; CANCER; DEGRADATION; MECHANISMS; HELICASE; EXCHANGE;
D O I
10.1016/j.dnarep.2023.103548
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The perturbation of DNA replication, a phenomena termed "replication stress", is a driving force of genome instability and a hallmark of cancer cells. Among the DNA repair mechanisms that contribute to tolerating replication stress, the homologous recombination pathway is central to the alteration of replication fork progression. In many organisms, defects in the homologous recombination machinery result in increased cell sensitivity to replication-blocking agents and a higher risk of cancer in humans. Moreover, the status of homologous recombination in cancer cells often correlates with the efficacy of anti-cancer treatment. In this review, we discuss our current understanding of the different functions of homologous recombination in fixing replication-associated DNA damage and contributing to complete genome duplication. We also examine which functions are pivotal in preventing cancer and genome instability.
引用
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页数:9
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