Distinct mechanisms of mutagenic processing of alternative DNA structures by repair proteins.

DNA repair DNA structure Non-B DNA cancer mutagenesis

Journal

Molecular & cellular oncology
ISSN: 2372-3556
Titre abrégé: Mol Cell Oncol
Pays: United States
ID NLM: 101642411

Informations de publication

Date de publication:
2020
Historique:
received: 05 03 2020
revised: 11 03 2020
accepted: 12 03 2020
entrez: 12 5 2020
pubmed: 12 5 2020
medline: 12 5 2020
Statut: epublish

Résumé

Repetitive sequences can form a variety of alternative DNA structures (non-B DNA) that can modulate transcription, replication, and repair. However, non-B DNA-forming sequences can also stimulate mutagenesis, and are enriched at mutation hotspots in human cancer genomes. Interestingly, different types of non-B DNA stimulate mutagenesis via distinct repair processing mechanisms.

Identifiants

pubmed: 32391433
doi: 10.1080/23723556.2020.1743807
pii: 1743807
pmc: PMC7199757
doi:

Types de publication

Journal Article

Langues

eng

Pagination

1743807

Subventions

Organisme : NCI NIH HHS
ID : R01 CA093729
Pays : United States

Informations de copyright

© 2020 The Author(s). Published with license by Taylor & Francis Group, LLC.

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Auteurs

Jennifer A McKinney (JA)

Division of Pharmacology and Toxicology, College of Pharmacy, The University of Texas at Austin, Dell Pediatric Research Institute, Austin, TX, USA.

Guliang Wang (G)

Division of Pharmacology and Toxicology, College of Pharmacy, The University of Texas at Austin, Dell Pediatric Research Institute, Austin, TX, USA.

Karen M Vasquez (KM)

Division of Pharmacology and Toxicology, College of Pharmacy, The University of Texas at Austin, Dell Pediatric Research Institute, Austin, TX, USA.

Classifications MeSH