Nucleosome Array Deformation in Chromatin is Sustained by Bending, Twisting and Kinking of Linker DNA.


Journal

Journal of molecular biology
ISSN: 1089-8638
Titre abrégé: J Mol Biol
Pays: Netherlands
ID NLM: 2985088R

Informations de publication

Date de publication:
15 10 2023
Historique:
received: 08 07 2023
revised: 21 08 2023
accepted: 30 08 2023
medline: 2 10 2023
pubmed: 8 9 2023
entrez: 7 9 2023
Statut: ppublish

Résumé

Chromatin in the nucleus undergoes mechanical stresses from different sources during the various stages of cell life. Here a trinucleosome array is used as the minimal model to study the mechanical response to applied stress at the molecular level. By using large-scale, all-atom steered-molecular dynamics simulations, we show that the largest part of mechanical stress in compression is accommodated by the DNA linkers joining pairs of nucleosomes, which store the elastic energy accumulated by the applied force. Different mechanical instabilities (Euler bending, Brazier kinking, twist-bending) can deform the DNA canonical structure, as a function of the increasing force load. An important role of the histone tails in assisting the DNA deformation is highlighted. The overall response of the smallest chromatin fragment to compressive stress leaves the nucleosome assembly with a substantial plastic deformation and localised defects, which can have a potential impact on DNA transcription, downstream signaling pathways, the regulation of gene expression, and DNA repair.

Identifiants

pubmed: 37678705
pii: S0022-2836(23)00374-1
doi: 10.1016/j.jmb.2023.168263
pii:
doi:

Substances chimiques

Chromatin 0
DNA 9007-49-2
Histones 0
Nucleosomes 0

Banques de données

figshare
['10.6084/m9.figshare.23634396']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

168263

Informations de copyright

Copyright © 2023. Published by Elsevier Ltd.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Fabrizio Cleri (F)

Université de Lille, Institut d'Electronique Microelectronique et Nanotechnologie (IEMN CNRS UMR8520) and Département de Physique, 59652 Villeneuve d'Ascq, France. Electronic address: fabrizio.cleri@univ-lille.fr.

Stefano Giordano (S)

University of Lille, CNRS, Centrale Lille, Univ. Polytechnique Hauts-de-France, UMR 8520 - IEMN - Institut d'Électronique de Microélectronique et de Nanotechnologie, F-59000 Lille, France.

Ralf Blossey (R)

Univ. Lille, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle, F-59000 Lille, France.

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Classifications MeSH