The regulation of DNA end resection by chromatin response to DNA double strand breaks.

53BP1 BRCA1 DNA end resection chromatin remodeling histone modificaitons homologous recombination non-homologous end joining

Journal

Frontiers in cell and developmental biology
ISSN: 2296-634X
Titre abrégé: Front Cell Dev Biol
Pays: Switzerland
ID NLM: 101630250

Informations de publication

Date de publication:
2022
Historique:
received: 30 04 2022
accepted: 29 06 2022
entrez: 1 8 2022
pubmed: 2 8 2022
medline: 2 8 2022
Statut: epublish

Résumé

DNA double-strand breaks (DSBs) constantly arise upon exposure to genotoxic agents and during physiological processes. The timely repair of DSBs is important for not only the completion of the cellular functions involving DSBs as intermediates, but also the maintenance of genome stability. There are two major pathways dedicated to DSB repair: homologous recombination (HR) and non-homologous end joining (NHEJ). The decision of deploying HR or NHEJ to repair DSBs largely depends on the structures of broken DNA ends. DNA ends resected to generate extensive single-strand DNA (ssDNA) overhangs are repaired by HR, while those remaining blunt or minimally processed can be repaired by NHEJ. As the generation and repair of DSB occurs within the context of chromatin, the resection of broken DNA ends is also profoundly affected by the state of chromatin flanking DSBs. Here we review how DNA end resection can be regulated by histone modifications, chromatin remodeling, and the presence of ssDNA structure through altering the accessibility to chromatin and the activity of pro- and anti-resection proteins.

Identifiants

pubmed: 35912102
doi: 10.3389/fcell.2022.932633
pii: 932633
pmc: PMC9335370
doi:

Types de publication

Journal Article Review

Langues

eng

Pagination

932633

Subventions

Organisme : NIAID NIH HHS
ID : R01 AI047829
Pays : United States

Informations de copyright

Copyright © 2022 Chen and Sleckman.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Bo-Ruei Chen (BR)

Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, United States.

Barry P Sleckman (BP)

Division of Hematology and Oncology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, United States.
O'Neal Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL, United States.

Classifications MeSH