Studying DNA Double-Strand Break Repair: An Ever-Growing Toolbox

被引:109
作者
Vitor, Alexandra C. [1 ]
Huertas, Pablo [2 ,3 ]
Legube, Gaelle [4 ]
de Almeida, Sergio F. [1 ]
机构
[1] Univ Lisbon, Inst Med Mol Joao Lobo Antunes, Fac Med, Lisbon, Portugal
[2] Univ Seville, Dept Genet, Seville, Spain
[3] Univ Pablo Olavide, Univ Sevilla, CSIC, Ctr Andaluz Biol Mol & Med Regenerat CABIMER, Seville, Spain
[4] Univ Toulouse, CNRS, CBI, LBCMCP, Toulouse, France
基金
欧洲研究理事会;
关键词
DNA repair; homologous recombination (HR); non-homologous DNA end joining; chromatin; DNA damage; DAMAGE-RESPONSE; HOMOLOGOUS RECOMBINATION; GENOME-WIDE; HUMAN-CELLS; CHROMATIN; ATM; DYNAMICS; TRANSCRIPTION; COMPLEX; 53BP1;
D O I
10.3389/fmolb.2020.00024
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To ward off against the catastrophic consequences of persistent DNA double-strand breaks (DSBs), eukaryotic cells have developed a set of complex signaling networks that detect these DNA lesions, orchestrate cell cycle checkpoints and ultimately lead to their repair. Collectively, these signaling networks comprise the DNA damage response (DDR). The current knowledge of the molecular determinants and mechanistic details of the DDR owes greatly to the continuous development of ground-breaking experimental tools that couple the controlled induction of DSBs at distinct genomic positions with assays and reporters to investigate DNA repair pathways, their impact on other DNA-templated processes and the specific contribution of the chromatin environment. In this review, we present these tools, discuss their pros and cons and illustrate their contribution to our current understanding of the DDR.
引用
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页数:16
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