Topoisomerase 1 facilitates nucleosome reassembly at stress genes during recovery.


Journal

Nucleic acids research
ISSN: 1362-4962
Titre abrégé: Nucleic Acids Res
Pays: England
ID NLM: 0411011

Informations de publication

Date de publication:
11 Dec 2023
Historique:
accepted: 25 10 2023
revised: 19 10 2023
received: 15 03 2023
pubmed: 13 11 2023
medline: 13 11 2023
entrez: 13 11 2023
Statut: ppublish

Résumé

Chromatin remodeling is essential to allow full development of alternative gene expression programs in response to environmental changes. In fission yeast, oxidative stress triggers massive transcriptional changes including the activation of hundreds of genes, with the participation of histone modifying complexes and chromatin remodelers. DNA transcription is associated to alterations in DNA topology, and DNA topoisomerases facilitate elongation along gene bodies. Here, we test whether the DNA topoisomerase Top1 participates in the RNA polymerase II-dependent activation of the cellular response to oxidative stress. Cells lacking Top1 are resistant to H2O2 stress. The transcriptome of Δtop1 strain was not greatly affected in the absence of stress, but activation of the anti-stress gene expression program was more sustained than in wild-type cells. Top1 associated to stress open reading frames. While the nucleosomes of stress genes are partially and transiently evicted during stress, the chromatin configuration remains open for longer times in cells lacking Top1, facilitating RNA polymerase II progression. We propose that, by removing DNA tension arising from transcription, Top1 facilitates nucleosome reassembly and works in synergy with the chromatin remodeler Hrp1 as opposing forces to transcription and to Snf22 / Hrp3 opening remodelers.

Identifiants

pubmed: 37956308
pii: 7416808
doi: 10.1093/nar/gkad1066
pmc: PMC10711424
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12161-12173

Subventions

Organisme : MCIN//AEI//10.13039//501
Organisme : ERDF
Organisme : European Union
Organisme : Generalitat de Catalunya
ID : 2017-SGR-539 and 2021-SGR-00007
Organisme : ICREA Academia Award
Organisme : Ministerio de Economía y Competitividad
Organisme : Ministerio de Ciencia e Innovación
ID : PID2021-122837-NB-I00

Informations de copyright

© The Author(s) 2023. Published by Oxford University Press on behalf of Nucleic Acids Research.

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Auteurs

Montserrat Vega (M)

Oxidative Stress and Cell Cycle Group, Universitat Pompeu Fabra, Barcelona 08003, Spain.

Rubén Barrios (R)

Oxidative Stress and Cell Cycle Group, Universitat Pompeu Fabra, Barcelona 08003, Spain.

Rodrigo Fraile (R)

Oxidative Stress and Cell Cycle Group, Universitat Pompeu Fabra, Barcelona 08003, Spain.

Kevin de Castro Cogle (K)

BatchX Inc., San Jose, CAUSA.

David Castillo (D)

BatchX Inc., San Jose, CAUSA.

Roger Anglada (R)

Genomics Core Facility, Universitat Pompeu Fabra, Barcelona 08003, Spain.

Ferran Casals (F)

Genomics Core Facility, Universitat Pompeu Fabra, Barcelona 08003, Spain.

José Ayté (J)

Oxidative Stress and Cell Cycle Group, Universitat Pompeu Fabra, Barcelona 08003, Spain.

Ernesto Lowy-Gallego (E)

European Molecular Biology Laboratory, European Bioinformatics Institute, Wellcome Genome Campus, Hinxton, Cambridge CB10 1SD, UK.

Elena Hidalgo (E)

Oxidative Stress and Cell Cycle Group, Universitat Pompeu Fabra, Barcelona 08003, Spain.

Classifications MeSH