Walking a tightrope The complex balancing act of R-loops in genome stability

被引:141
作者
Brickner, Joshua R. [1 ]
Garzon, Jada L. [1 ]
Cimprich, Karlene A. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Chem & Syst Biol, Stanford, CA 94305 USA
基金
美国国家卫生研究院;
关键词
RNA-POLYMERASE-II; DNA-END RESECTION; TRANSCRIPTIONAL PAUSE SITES; STRAND BREAK REPAIR; HOMOLOGOUS RECOMBINATION; REPLICATION INITIATION; PATTERN-RECOGNITION; CHECKPOINT KINASE; CRYSTAL-STRUCTURE; RNA/DNA HYBRIDS;
D O I
10.1016/j.molcel.2022.04.014
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
Although transcription is an essential cellular process, it is paradoxically also a well-recognized cause of genomic instability. R-loops, non-B DNA structures formed when nascent RNA hybridizes to DNA to displace the non-template strand as single-stranded DNA (ssDNA), are partially responsible for this instability. Yet, recent work has begun to elucidate regulatory roles for R-loops in maintaining the genome. In this review, we discuss the cellular contexts in which R-loops contribute to genomic instability, particularly during DNA replication and double-strand break (DSB) repair. We also summarize the evidence that R-loops participate as an intermediate during repair and may influence pathway choice to preserve genomic integrity. Finally, we discuss the immunogenic potential of R-loops and highlight their links to disease should they become pathogenic.
引用
收藏
页码:2267 / 2297
页数:31
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