RNA at DNA Double-Strand Breaks: The Challenge of Dealing with DNA
Number of Authors: 32020 (English)In: Bioessays, ISSN 0265-9247, E-ISSN 1521-1878, Vol. 42, no 5, article id 1900225Article, review/survey (Refereed) Published
Abstract [en]
RNA polymerase II is recruited to DNA double-strand breaks (DSBs), transcribes the sequences that flank the break and produces a novel RNA type that has been termed damage-induced long non-coding RNA (dilncRNA). DilncRNAs can be processed into short, miRNA-like molecules or degraded by different ribonucleases. They can also form double-stranded RNAs or DNA:RNA hybrids. The DNA:RNA hybrids formed at DSBs contribute to the recruitment of repair factors during the early steps of homologous recombination (HR) and, in this way, contribute to the accuracy of the DNA repair. However, if not resolved, the DNA:RNA hybrids are highly mutagenic and prevent the recruitment of later HR factors. Here recent discoveries about the synthesis, processing, and degradation of dilncRNAs are revised. The focus is on RNA clearance, a necessary step for the successful repair of DSBs and the aim is to reconcile contradictory findings on the effects of dilncRNAs and DNA:RNA hybrids in HR.
Place, publisher, year, edition, pages
2020. Vol. 42, no 5, article id 1900225
Keywords [en]
DNA repair, EXOSC10, exosome, homologous recombination, RNA clearance, RNAse H, transcription
National Category
Biological Sciences
Identifiers
URN: urn:nbn:se:su:diva-180366DOI: 10.1002/bies.201900225ISI: 000516663600001PubMedID: 32105369OAI: oai:DiVA.org:su-180366DiVA, id: diva2:1421490
2020-04-032020-04-032022-03-23Bibliographically approved