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Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates

Replication of vertebrate genomes is tightly regulated to ensure accurate duplication, but our understanding of the interplay between genetic and epigenetic factors in this regulation remains incomplete. Here, we investigated the involvement of three elements enriched at gene promoters and replicati...

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Autores principales: Poulet-Benedetti, Jérémy, Tonnerre-Doncarli, Caroline, Valton, Anne-Laure, Laurent, Marc, Gérard, Marie, Barinova, Natalja, Parisis, Nikolaos, Massip, Florian, Picard, Franck, Prioleau, Marie-Noëlle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415359/
https://www.ncbi.nlm.nih.gov/pubmed/37563125
http://dx.doi.org/10.1038/s41467-023-40441-4
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author Poulet-Benedetti, Jérémy
Tonnerre-Doncarli, Caroline
Valton, Anne-Laure
Laurent, Marc
Gérard, Marie
Barinova, Natalja
Parisis, Nikolaos
Massip, Florian
Picard, Franck
Prioleau, Marie-Noëlle
author_facet Poulet-Benedetti, Jérémy
Tonnerre-Doncarli, Caroline
Valton, Anne-Laure
Laurent, Marc
Gérard, Marie
Barinova, Natalja
Parisis, Nikolaos
Massip, Florian
Picard, Franck
Prioleau, Marie-Noëlle
author_sort Poulet-Benedetti, Jérémy
collection PubMed
description Replication of vertebrate genomes is tightly regulated to ensure accurate duplication, but our understanding of the interplay between genetic and epigenetic factors in this regulation remains incomplete. Here, we investigated the involvement of three elements enriched at gene promoters and replication origins: guanine-rich motifs potentially forming G-quadruplexes (pG4s), nucleosome-free regions (NFRs), and the histone variant H2A.Z, in the firing of origins of replication in vertebrates. We show that two pG4s on the same DNA strand (dimeric pG4s) are sufficient to induce the assembly of an efficient minimal replication origin without inducing transcription in avian DT40 cells. Dimeric pG4s in replication origins are associated with formation of an NFR next to precisely-positioned nucleosomes enriched in H2A.Z on this minimal origin and genome-wide. Thus, our data suggest that dimeric pG4s are important for the organization and duplication of vertebrate genomes. It supports the hypothesis that a nucleosome close to an NFR is a shared signal for the formation of replication origins in eukaryotes.
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spelling pubmed-104153592023-08-12 Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates Poulet-Benedetti, Jérémy Tonnerre-Doncarli, Caroline Valton, Anne-Laure Laurent, Marc Gérard, Marie Barinova, Natalja Parisis, Nikolaos Massip, Florian Picard, Franck Prioleau, Marie-Noëlle Nat Commun Article Replication of vertebrate genomes is tightly regulated to ensure accurate duplication, but our understanding of the interplay between genetic and epigenetic factors in this regulation remains incomplete. Here, we investigated the involvement of three elements enriched at gene promoters and replication origins: guanine-rich motifs potentially forming G-quadruplexes (pG4s), nucleosome-free regions (NFRs), and the histone variant H2A.Z, in the firing of origins of replication in vertebrates. We show that two pG4s on the same DNA strand (dimeric pG4s) are sufficient to induce the assembly of an efficient minimal replication origin without inducing transcription in avian DT40 cells. Dimeric pG4s in replication origins are associated with formation of an NFR next to precisely-positioned nucleosomes enriched in H2A.Z on this minimal origin and genome-wide. Thus, our data suggest that dimeric pG4s are important for the organization and duplication of vertebrate genomes. It supports the hypothesis that a nucleosome close to an NFR is a shared signal for the formation of replication origins in eukaryotes. Nature Publishing Group UK 2023-08-10 /pmc/articles/PMC10415359/ /pubmed/37563125 http://dx.doi.org/10.1038/s41467-023-40441-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Poulet-Benedetti, Jérémy
Tonnerre-Doncarli, Caroline
Valton, Anne-Laure
Laurent, Marc
Gérard, Marie
Barinova, Natalja
Parisis, Nikolaos
Massip, Florian
Picard, Franck
Prioleau, Marie-Noëlle
Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates
title Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates
title_full Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates
title_fullStr Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates
title_full_unstemmed Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates
title_short Dimeric G-quadruplex motifs-induced NFRs determine strong replication origins in vertebrates
title_sort dimeric g-quadruplex motifs-induced nfrs determine strong replication origins in vertebrates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10415359/
https://www.ncbi.nlm.nih.gov/pubmed/37563125
http://dx.doi.org/10.1038/s41467-023-40441-4
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