DNA polymerase ζ has robust reverse transcriptase activity relative to other cellular DNA polymerases.

DNA polymerase zeta DNA synthesis double-strand DNA break repair reverse transcriptase translesion DNA polymerase

Journal

The Journal of biological chemistry
ISSN: 1083-351X
Titre abrégé: J Biol Chem
Pays: United States
ID NLM: 2985121R

Informations de publication

Date de publication:
23 Oct 2024
Historique:
received: 25 06 2024
revised: 29 09 2024
accepted: 10 10 2024
medline: 26 10 2024
pubmed: 26 10 2024
entrez: 25 10 2024
Statut: aheadofprint

Résumé

Cell biology and genetic studies have demonstrated that DNA double strand break (DSB) repair can be performed using an RNA transcript that spans the site of the DNA break as a template for repair. This type of DSB repair requires a reverse transcriptase to convert an RNA sequence into DNA to facilitate repair of the break, rather than copying from a DNA template as in canonical DSB repair. Translesion synthesis (TLS) DNA polymerases (Pol) are often more promiscuous than DNA Pols, raising the notion that reverse transcription could be performed by a TLS Pol. Indeed, several studies have demonstrated that human Pol η has reverse transcriptase activity, while others have suggested that the yeast TLS Pol ζ is involved. Here, we purify all seven known nuclear DNA Pols of Saccharomyces cerevisiae and compare their reverse transcriptase activities. The comparison shows that Pol ζ far surpasses Pol η and all other DNA Pols in reverse transcriptase activity. We find that Pol ζ reverse transcriptase activity is not affected by RPA or RFC/PCNA and acts distributively to make DNA complementary to an RNA template strand. Consistent with prior S. cerevisiae studies performed in vivo, we propose that Pol ζ is the major DNA Pol that functions in the RNA templated DSB repair pathway.

Identifiants

pubmed: 39454951
pii: S0021-9258(24)02420-7
doi: 10.1016/j.jbc.2024.107918
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

107918

Informations de copyright

Copyright © 2024 The Authors. Published by Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of Interest “The authors declare that they have no conflicts of interest with the contents of this article.”

Auteurs

Ryan Mayle (R)

Howard Hughes Medical Institute and the Department of DNA Replication, The Rockefeller University New York, NY 10065.

William K Holloman (WK)

Department of Microbiology & Immunology, Weill Cornell Medicine, New York, NY 10065. Electronic address: wkhollo@med.cornell.edu.

Michael E O'Donnell (ME)

Howard Hughes Medical Institute and the Department of DNA Replication, The Rockefeller University New York, NY 10065. Electronic address: odonnel@rockefeller.edu.

Classifications MeSH