Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin Remodeling

Nucleosomes are structural units of the chromosome consisting of DNA wrapped around histone proteins, and play important roles in compaction and regulation of the chromatin structure. While the structure and dynamics of canonical nucleosomes have been studied extensively, those of nucleosomes in int...

Full description

Bibliographic Details
Main Authors: Takeru Kameda, Akinori Awazu, Yuichi Togashi
Format: Article
Language:English
Published: Frontiers Media S.A. 2019-11-01
Series:Frontiers in Molecular Biosciences
Subjects:
DNA
Online Access:https://www.frontiersin.org/article/10.3389/fmolb.2019.00133/full
id doaj-d598b6f37b39483fa13b07e10e883e0b
record_format Article
spelling doaj-d598b6f37b39483fa13b07e10e883e0b2020-11-25T01:59:46ZengFrontiers Media S.A.Frontiers in Molecular Biosciences2296-889X2019-11-01610.3389/fmolb.2019.00133486330Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin RemodelingTakeru Kameda0Akinori Awazu1Akinori Awazu2Yuichi Togashi3Yuichi Togashi4Yuichi Togashi5Department of Mathematical and Life Sciences, Graduate School of Science, Hiroshima University, Higashi-Hiroshima, JapanGraduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, JapanResearch Center for the Mathematics on Chromatin Live Dynamics (RcMcD), Hiroshima University, Higashi-Hiroshima, JapanGraduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, JapanResearch Center for the Mathematics on Chromatin Live Dynamics (RcMcD), Hiroshima University, Higashi-Hiroshima, JapanRIKEN Center for Biosystems Dynamics Research (BDR), Higashi-Hiroshima, JapanNucleosomes are structural units of the chromosome consisting of DNA wrapped around histone proteins, and play important roles in compaction and regulation of the chromatin structure. While the structure and dynamics of canonical nucleosomes have been studied extensively, those of nucleosomes in intermediate states, that occur when their structure or positioning is modulated, have been less understood. In particular, the dynamic features of partially disassembled nucleosomes have not been discussed in previous studies. Using all-atom molecular dynamics simulations, in this study, we investigated the dynamics and stability of nucleosome structures lacking a histone-dimer. DNA in nucleosomes lacking a histone H2A/H2B dimer was drastically deformed due to loss of local interactions between DNA and histones. In contrast, conformation of DNA in nucleosomes lacking H3/H4 was similar to the canonical nucleosome, as the H2A C-terminal domain infiltrated the space originally occupied by the dissociated H3/H4 histones and restricted DNA dynamics in close proximity. Our results suggest that, besides histone chaperones, the intrinsic dynamics of nucleosomes support the exchange of H2A/H2B, which is significantly more frequent than that of H3/H4.https://www.frontiersin.org/article/10.3389/fmolb.2019.00133/fullnucleosomeDNAhistonechromatinstructural dynamicshexasome
collection DOAJ
language English
format Article
sources DOAJ
author Takeru Kameda
Akinori Awazu
Akinori Awazu
Yuichi Togashi
Yuichi Togashi
Yuichi Togashi
spellingShingle Takeru Kameda
Akinori Awazu
Akinori Awazu
Yuichi Togashi
Yuichi Togashi
Yuichi Togashi
Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin Remodeling
Frontiers in Molecular Biosciences
nucleosome
DNA
histone
chromatin
structural dynamics
hexasome
author_facet Takeru Kameda
Akinori Awazu
Akinori Awazu
Yuichi Togashi
Yuichi Togashi
Yuichi Togashi
author_sort Takeru Kameda
title Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin Remodeling
title_short Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin Remodeling
title_full Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin Remodeling
title_fullStr Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin Remodeling
title_full_unstemmed Histone Tail Dynamics in Partially Disassembled Nucleosomes During Chromatin Remodeling
title_sort histone tail dynamics in partially disassembled nucleosomes during chromatin remodeling
publisher Frontiers Media S.A.
series Frontiers in Molecular Biosciences
issn 2296-889X
publishDate 2019-11-01
description Nucleosomes are structural units of the chromosome consisting of DNA wrapped around histone proteins, and play important roles in compaction and regulation of the chromatin structure. While the structure and dynamics of canonical nucleosomes have been studied extensively, those of nucleosomes in intermediate states, that occur when their structure or positioning is modulated, have been less understood. In particular, the dynamic features of partially disassembled nucleosomes have not been discussed in previous studies. Using all-atom molecular dynamics simulations, in this study, we investigated the dynamics and stability of nucleosome structures lacking a histone-dimer. DNA in nucleosomes lacking a histone H2A/H2B dimer was drastically deformed due to loss of local interactions between DNA and histones. In contrast, conformation of DNA in nucleosomes lacking H3/H4 was similar to the canonical nucleosome, as the H2A C-terminal domain infiltrated the space originally occupied by the dissociated H3/H4 histones and restricted DNA dynamics in close proximity. Our results suggest that, besides histone chaperones, the intrinsic dynamics of nucleosomes support the exchange of H2A/H2B, which is significantly more frequent than that of H3/H4.
topic nucleosome
DNA
histone
chromatin
structural dynamics
hexasome
url https://www.frontiersin.org/article/10.3389/fmolb.2019.00133/full
work_keys_str_mv AT takerukameda histonetaildynamicsinpartiallydisassemblednucleosomesduringchromatinremodeling
AT akinoriawazu histonetaildynamicsinpartiallydisassemblednucleosomesduringchromatinremodeling
AT akinoriawazu histonetaildynamicsinpartiallydisassemblednucleosomesduringchromatinremodeling
AT yuichitogashi histonetaildynamicsinpartiallydisassemblednucleosomesduringchromatinremodeling
AT yuichitogashi histonetaildynamicsinpartiallydisassemblednucleosomesduringchromatinremodeling
AT yuichitogashi histonetaildynamicsinpartiallydisassemblednucleosomesduringchromatinremodeling
_version_ 1724962649240764416