Literature DB >> 28877499

H4 Tails Potentially Produce the Diversity in the Orientation of Two Nucleosomes.

Hisashi Ishida1, Hidetoshi Kono2.   

Abstract

Histone tails play an important role in internucleosomal interaction and chromatin compaction. To understand how the H4 tails are involved in the internucleosomal interaction, an adaptively biased molecular dynamics simulation of 63 models of two stacked nucleosomes, each with the H4 tails in different locations, was carried out. This simulation generated a variety of orientations of the separated nucleosomes depending on the formation of the H4 tail bridge between the H4 tails and the DNA of the neighboring nucleosomes. For the models that showed distinctive orientations of the two nucleosomes, the free energies of the separation of the nucleosomes were further investigated using umbrella sampling simulations. The attractive force between the nucleosomes was estimated from the free energies; the force when two H4 tail bridges formed varied from 36 to 63 pN, depending on the formation of the H4 tail-bridge and the interfacial interaction, whereas the force reduced to 15-18 pN after either one of the H4 tail bridges had broken, regardless of the conformation of the H4 tail. Additional simulations of the nucleosomes show that when the H4 tail was truncated, the force between the nucleosomes became repulsive (from-3 to -7 pN). We concluded that the H4 tails potentially produce the diversity in the orientation of the two nucleosomes, which would contribute to the polymorphism of the chromatin structure.
Copyright © 2017 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2017        PMID: 28877499      PMCID: PMC5611672          DOI: 10.1016/j.bpj.2017.07.015

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  51 in total

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Authors:  Nikolay Korolev; Alexander P Lyubartsev; Lars Nordenskiöld
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4.  Crystal structure of the nucleosome core particle at 2.8 A resolution.

Authors:  K Luger; A W Mäder; R K Richmond; D F Sargent; T J Richmond
Journal:  Nature       Date:  1997-09-18       Impact factor: 49.962

5.  A distinct switch in interactions of the histone H4 tail domain upon salt-dependent folding of nucleosome arrays.

Authors:  Sharon Pepenella; Kevin J Murphy; Jeffrey J Hayes
Journal:  J Biol Chem       Date:  2014-08-13       Impact factor: 5.157

6.  Modeling studies of chromatin fiber structure as a function of DNA linker length.

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Authors:  Faye Gordon; Karolin Luger; Jeffrey C Hansen
Journal:  J Biol Chem       Date:  2005-07-19       Impact factor: 5.157

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Authors:  Yanping Fan; Nikolay Korolev; Alexander P Lyubartsev; Lars Nordenskiöld
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  7 in total

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4.  Free energy profiles for unwrapping the outer superhelical turn of nucleosomal DNA.

Authors:  Hidetoshi Kono; Shun Sakuraba; Hisashi Ishida
Journal:  PLoS Comput Biol       Date:  2018-03-05       Impact factor: 4.475

5.  A multiscale analysis of DNA phase separation: from atomistic to mesoscale level.

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6.  Interactions Between Nucleosomes: From Atomistic Simulation to Polymer Model.

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Journal:  Front Mol Biosci       Date:  2021-04-12

7.  Cryo-EM of nucleosome core particle interactions in trans.

Authors:  Silvija Bilokapic; Mike Strauss; Mario Halic
Journal:  Sci Rep       Date:  2018-05-04       Impact factor: 4.379

  7 in total

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