Abstract
Since their discovery, R‐loops have been associated with both physiological and pathological functions that are conserved across species. R‐loops are a source of replication stress and genome instability, as seen in neurodegenerative disorders and cancer. In response, cells have evolved pathways to prevent R‐loop accumulation as well as to resolve them. A growing body of evidence correlates R‐loop accumulation with changes in the epigenetic landscape. However, the role of chromatin modification and remodeling in R‐loops homeostasis remains unclear. This review covers various mechanisms precluding R‐loop accumulation and highlights the role of chromatin modifiers and remodelers in facilitating timely R‐loop resolution. We also discuss the enigmatic role of RNA:DNA hybrids in facilitating DNA repair, epigenetic landscape and the potential role of replication fork preservation pathways, active fork stability and stalled fork protection pathways, in avoiding replication‐transcription conflicts. Finally, we discuss the potential role of several Chro‐ Mates (chromatin modifiers and remodelers) in the likely differentiation between persistent/detri-mental R‐loops and transient/benign R‐loops that assist in various physiological processes relevant for therapeutic interventions.
Original language | English |
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Article number | 8850 |
Journal | International Journal of Molecular Sciences |
Volume | 22 |
Issue number | 16 |
DOIs | |
Publication status | Published - 17 Aug 2021 |
Bibliographical note
Funding Information:Funding: This research is supported by NWO‐Incentive Grant (12412) to N.T.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.