Cargando…
Histone dynamics mediate DNA unwrapping and sliding in nucleosomes
Nucleosomes are elementary building blocks of chromatin in eukaryotes. They tightly wrap ∼147 DNA base pairs around an octamer of histone proteins. How nucleosome structural dynamics affect genome functioning is not completely clear. Here we report all-atom molecular dynamics simulations of nucleoso...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062685/ https://www.ncbi.nlm.nih.gov/pubmed/33888707 http://dx.doi.org/10.1038/s41467-021-22636-9 |
_version_ | 1783681811352649728 |
---|---|
author | Armeev, Grigoriy A. Kniazeva, Anastasiia S. Komarova, Galina A. Kirpichnikov, Mikhail P. Shaytan, Alexey K. |
author_facet | Armeev, Grigoriy A. Kniazeva, Anastasiia S. Komarova, Galina A. Kirpichnikov, Mikhail P. Shaytan, Alexey K. |
author_sort | Armeev, Grigoriy A. |
collection | PubMed |
description | Nucleosomes are elementary building blocks of chromatin in eukaryotes. They tightly wrap ∼147 DNA base pairs around an octamer of histone proteins. How nucleosome structural dynamics affect genome functioning is not completely clear. Here we report all-atom molecular dynamics simulations of nucleosome core particles at a timescale of 15 microseconds. At this timescale, functional modes of nucleosome dynamics such as spontaneous nucleosomal DNA breathing, unwrapping, twisting, and sliding were observed. We identified atomistic mechanisms of these processes by analyzing the accompanying structural rearrangements of the histone octamer and histone-DNA contacts. Octamer dynamics and plasticity were found to enable DNA unwrapping and sliding. Through multi-scale modeling, we showed that nucleosomal DNA dynamics contribute to significant conformational variability of the chromatin fiber at the supranucleosomal level. Our study further supports mechanistic coupling between fine details of histone dynamics and chromatin functioning, provides a framework for understanding the effects of various chromatin modifications. |
format | Online Article Text |
id | pubmed-8062685 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80626852021-05-11 Histone dynamics mediate DNA unwrapping and sliding in nucleosomes Armeev, Grigoriy A. Kniazeva, Anastasiia S. Komarova, Galina A. Kirpichnikov, Mikhail P. Shaytan, Alexey K. Nat Commun Article Nucleosomes are elementary building blocks of chromatin in eukaryotes. They tightly wrap ∼147 DNA base pairs around an octamer of histone proteins. How nucleosome structural dynamics affect genome functioning is not completely clear. Here we report all-atom molecular dynamics simulations of nucleosome core particles at a timescale of 15 microseconds. At this timescale, functional modes of nucleosome dynamics such as spontaneous nucleosomal DNA breathing, unwrapping, twisting, and sliding were observed. We identified atomistic mechanisms of these processes by analyzing the accompanying structural rearrangements of the histone octamer and histone-DNA contacts. Octamer dynamics and plasticity were found to enable DNA unwrapping and sliding. Through multi-scale modeling, we showed that nucleosomal DNA dynamics contribute to significant conformational variability of the chromatin fiber at the supranucleosomal level. Our study further supports mechanistic coupling between fine details of histone dynamics and chromatin functioning, provides a framework for understanding the effects of various chromatin modifications. Nature Publishing Group UK 2021-04-22 /pmc/articles/PMC8062685/ /pubmed/33888707 http://dx.doi.org/10.1038/s41467-021-22636-9 Text en © The Author(s) 2021 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Armeev, Grigoriy A. Kniazeva, Anastasiia S. Komarova, Galina A. Kirpichnikov, Mikhail P. Shaytan, Alexey K. Histone dynamics mediate DNA unwrapping and sliding in nucleosomes |
title | Histone dynamics mediate DNA unwrapping and sliding in nucleosomes |
title_full | Histone dynamics mediate DNA unwrapping and sliding in nucleosomes |
title_fullStr | Histone dynamics mediate DNA unwrapping and sliding in nucleosomes |
title_full_unstemmed | Histone dynamics mediate DNA unwrapping and sliding in nucleosomes |
title_short | Histone dynamics mediate DNA unwrapping and sliding in nucleosomes |
title_sort | histone dynamics mediate dna unwrapping and sliding in nucleosomes |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8062685/ https://www.ncbi.nlm.nih.gov/pubmed/33888707 http://dx.doi.org/10.1038/s41467-021-22636-9 |
work_keys_str_mv | AT armeevgrigoriya histonedynamicsmediatednaunwrappingandslidinginnucleosomes AT kniazevaanastasiias histonedynamicsmediatednaunwrappingandslidinginnucleosomes AT komarovagalinaa histonedynamicsmediatednaunwrappingandslidinginnucleosomes AT kirpichnikovmikhailp histonedynamicsmediatednaunwrappingandslidinginnucleosomes AT shaytanalexeyk histonedynamicsmediatednaunwrappingandslidinginnucleosomes |