RAD51 Gene Family Structure and Function

被引:145
作者
Bonilla, Braulio [1 ]
Hengel, Sarah R. [1 ]
Grundy, McKenzie K. [1 ]
Bernstein, Kara A. [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Microbiol & Mol Genet, Pittsburgh, PA 15213 USA
来源
ANNUAL REVIEW OF GENETICS, VOL 54, 2020 | 2020年 / 54卷
基金
美国国家卫生研究院;
关键词
RAD51; paralog; double-strand break repair; homologous recombination; replication; Shu complex; REPLICATION PROTEIN-A; DOUBLE-STRAND BREAKS; EFFICIENT HOMOLOGOUS RECOMBINATION; CANCER SUSCEPTIBILITY GENE; DNA END RESECTION; SHU COMPLEX; NUCLEOPROTEIN FILAMENT; MEIOTIC RECOMBINATION; FANCONI-ANEMIA; FORK REVERSAL;
D O I
10.1146/annurev-genet-021920-092410
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Accurate DNA repair and replication are critical for genomic stability and cancer prevention. RAD51 and its gene family are key regulators of DNA fidelity through diverse roles in double-strand break repair, replication stress, and meiosis. RAD51 is an ATPase that forms a nucleoprotein filament on single-stranded DNA. RAD51 has the function of finding and invading homologous DNA sequences to enable accurate and timely DNA repair. Its paralogs, which arose from ancient gene duplications of RAD51, have evolved to regulate and promote RAD51 function. Underscoring its importance, misregulation of RAD51, and its paralogs, is associated with diseases such as cancer and Fanconi anemia. In this review, we focus on the mammalian RAD51 structure and function and highlight the use of model systems to enable mechanistic understanding of RAD51 cellular roles. We also discuss how misregulation of the RAD51 gene family members contributes to disease and consider new approaches to pharmacologically inhibit RAD51.
引用
收藏
页码:25 / 46
页数:22
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