| Literature DB >> 35508167 |
Joshua R Brickner1, Jada L Garzon1, Karlene A Cimprich2.
Abstract
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.Entities:
Keywords: DNA damage; R-loop pathology; R-loops; RNA-DNA hybrid; double-strand break repair; genome stability; replication stress
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Year: 2022 PMID: 35508167 PMCID: PMC9233011 DOI: 10.1016/j.molcel.2022.04.014
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 19.328