Non-canonical DNA/RNA structures during Transcription-Coupled Double-Strand Break Repair: Roadblocks or Bona fide repair intermediates?


Journal

DNA repair
ISSN: 1568-7856
Titre abrégé: DNA Repair (Amst)
Pays: Netherlands
ID NLM: 101139138

Informations de publication

Date de publication:
09 2019
Historique:
pubmed: 25 7 2019
medline: 25 3 2020
entrez: 24 7 2019
Statut: ppublish

Résumé

Although long overlooked, it is now well understood that DNA does not systematically assemble into a canonical double helix, known as B-DNA, throughout the entire genome but can also accommodate other structures including DNA hairpins, G-quadruplexes and RNA:DNA hybrids. Notably, these non-canonical DNA structures form preferentially at transcriptionally active loci. Acting as replication roadblocks and being targeted by multiple machineries, these structures weaken the genome and render it prone to damage, including DNA double-strand breaks (DSB). In addition, secondary structures also further accumulate upon DSB formation. Here we discuss the potential functions of pre-existing or de novo formed nucleic acid structures, as bona fide repair intermediates or repair roadblocks, especially during Transcription-Coupled DNA Double-Strand Break repair (TC-DSBR), and provide an update on the specialized protein complexes displaying the ability to remove these structures to safeguard genome integrity.

Identifiants

pubmed: 31331819
pii: S1568-7864(19)30214-9
doi: 10.1016/j.dnarep.2019.102661
pmc: PMC6764918
mid: NIHMS1535270
pii:
doi:

Substances chimiques

RNA 63231-63-0
DNA 9007-49-2

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

102661

Subventions

Organisme : NCI NIH HHS
ID : R01 CA198279
Pays : United States
Organisme : NCI NIH HHS
ID : R01 CA201268
Pays : United States

Informations de copyright

Copyright © 2019 Elsevier B.V. All rights reserved.

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Auteurs

Nadine Puget (N)

LBCMCP, Centre de Biologie Integrative (CBI), CNRS, Université de Toulouse, UT3, France.

Kyle M Miller (KM)

Department of Molecular Biosciences, LIVESTRONG Cancer Institute of the Dell Medical School, Institute for Cellular and Molecular Biology, The University of Texas at Austin, Austin, TX, 78712, USA. Electronic address: kyle.miller@austin.utexas.edu.

Gaëlle Legube (G)

LBCMCP, Centre de Biologie Integrative (CBI), CNRS, Université de Toulouse, UT3, France. Electronic address: gaelle.legube@univ-tlse3.fr.

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