Moving forward one step back at a time: reversibility during homologous recombination

被引:30
作者
Piazza, Aurele [1 ]
Heyer, Wolf-Dietrich [2 ,3 ]
机构
[1] Inst Pasteur, Spatial Regulat Genomes, CNRS, UMR3525, 28 Rue Docteur Roux, F-75015 Paris, France
[2] Univ Calif Davis, Dept Microbiol & Mol Genet, One Shields Ave, Davis, CA 95616 USA
[3] Univ Calif Davis, Dept Mol & Cellular Biol, One Shields Ave, Davis, CA 95616 USA
关键词
D-loop; Homologous recombination; Helicase; Homology search; Genomic stability; Crossover; STRAND BREAK REPAIR; DOUBLE HOLLIDAY JUNCTIONS; MITOTIC RECOMBINATION; INDUCED REPLICATION; GENOME INSTABILITY; HALF-CROSSOVERS; MPH1; HELICASE; CROSSING-OVER; DNA-SYNTHESIS; D-LOOPS;
D O I
10.1007/s00294-019-00995-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
DNA double-strand breaks are genotoxic lesions whose repair can be templated off an intact DNA duplex through the conserved homologous recombination (HR) pathway. Because it mainly consists of a succession of non-covalent associations of molecules, HR is intrinsically reversible. Reversibility serves as an integral property of HR, exploited and tuned at various stages throughout the pathway with anti- and pro-recombinogenic consequences. Here, we focus on the reversibility of displacement loops (D-loops), a central DNA joint molecule intermediate whose dynamics and regulation have recently been physically probed in somatic S. cerevisiae cells. From homology search to repair completion, we discuss putative roles of D-loop reversibility in repair fidelity and outcome.
引用
收藏
页码:1333 / 1340
页数:8
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