Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
RNA at DNA Double-Strand Breaks: The Challenge of Dealing with DNA
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute. Parc Científic de Barcelona, Spain.
Stockholm University, Faculty of Science, Department of Biochemistry and Biophysics.
Stockholm University, Faculty of Science, Department of Molecular Biosciences, The Wenner-Gren Institute.
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
Available from: 2020-04-03 Created: 2020-04-03 Last updated: 2022-03-23Bibliographically approved

Open Access in DiVA

No full text in DiVA

Other links

Publisher's full textPubMed

Authority records

Bonath, FranziskaVisa, Neus

Search in DiVA

By author/editor
Bonath, FranziskaVisa, Neus
By organisation
Department of Molecular Biosciences, The Wenner-Gren InstituteDepartment of Biochemistry and Biophysics
In the same journal
Bioessays
Biological Sciences

Search outside of DiVA

GoogleGoogle Scholar

doi
pubmed
urn-nbn

Altmetric score

doi
pubmed
urn-nbn
Total: 34 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association-8th-edition
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf