Nucleosome simulations suggest mechanisms of electrostatically-driven mesoscale chromatin evolution
Abstract
Nucleosomes are structures made up of proteins called histones that bind and compact DNA, driving the mesoscale organization of the chromatin polymer. Although histone proteins have diversified over evolutionary time, their contributions to the corresponding diversification of chromatin structure are poorly understood. Here, we mine protein databases for histones and create \emph{in silico} nucleosomes for 3241 organisms spanning >1.5B years of evolution. Using a combination of electrostatic calculations and coarse-grained molecular dynamics simulations, we reveal extensive biophysical diversification of the nucleosome unit. Finally, we perform coarse-grained oligonucleosomal simulations on a subset of evolutionarily and biophysically divergent nucleosomes, demonstrating dramatic differences in bulk phase behavior of chromatin. Taken together, our results suggest a paradigm in which histones may have evolved to facilitate particular types of mesoscale chromatin behavior.
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BibTeX
@misc{jena2026nucleosome,
title = {{Nucleosome simulations suggest mechanisms of electrostatically-driven mesoscale chromatin evolution}},
author = {Siddhartha G. Jena},
howpublished = {arXiv},
year = {2026},
month = sep,
doi = {10.48550/arxiv.2609.24907},
eprint = {2609.24907},
archivePrefix = {arXiv},
url = {https://arxiv.org/abs/2609.24907},
note = {CC BY 4.0},
}
RIS
TY - UNPB
TI - Nucleosome simulations suggest mechanisms of electrostatically-driven mesoscale chromatin evolution
AU - Siddhartha G. Jena
PY - 2026
DA - 2026/09/21
PB - arXiv
DO - 10.48550/arxiv.2609.24907
UR - https://arxiv.org/abs/2609.24907
AB - Nucleosomes are structures made up of proteins called histones that bind and compact DNA, driving the mesoscale organization of the chromatin polymer. Although histone proteins have diversified over evolutionary time, their contributions to the corresponding diversification of chromatin structure are poorly understood. Here, we mine protein databases for histones and create \emph{in silico} nucleosomes for 3241 organisms spanning >1.5B years of evolution. Using a combination of electrostatic calculations and coarse-grained molecular dynamics simulations, we reveal extensive biophysical diversification of the nucleosome unit. Finally, we perform coarse-grained oligonucleosomal simulations on a subset of evolutionarily and biophysically divergent nucleosomes, demonstrating dramatic differences in bulk phase behavior of chromatin. Taken together, our results suggest a paradigm in which histones may have evolved to facilitate particular types of mesoscale chromatin behavior.
ER -