Abstract

Sharp increase in macromolecular crowding induces abnormal chromatin compaction in the cell nucleus, suggesting its non-negligible impact on chromatin structure and function. However, the details of the crowding-induced chromatin compaction remain poorly understood. In this work, we present a computer simulation study on the entropic effect of macromolecular crowding on the interaction between chromatin structural units called nucleosome clutches. Nucleosome clutches were modeled by a chain of nucleosomes collapsed by harmonic restraints implicitly mimicking the nucleosome association mediated by histone tails and linker histones. The nucleosome density of the clutches was set close to either that of high-density heterochromatin or that of low-density euchromatin. The effective interactions between these nucleosome clutches were calculated in various crowding conditions, and it was found that the increase in the degree of macromolecular crowding induced attractive interaction between two clutches with high nucleosome density. Interestingly, the increased degree of macromolecular crowding did not induce any attraction between two clutches with low nucleosome density. Our results suggest that the entropic effect of macromolecular crowding can enhance binding between nucleosome clutches in heterochromatin, but not in euchromatin, as a result of the difference in nucleosome packing degrees.

Highlights

  • Cellular environments are highly crowded with biological macromolecules, such as proteins and RNAs, and it was shown that the change in the degree of macromolecular crowding could significantly influence the structural and dynamic properties of diverse biological processes[1,2,3,4,5]

  • Our simulation results using the two models of nucleosome clutches revealed that the macromolecular crowding can have distinguishable entropic influences on structural units of euchromatin and heterochromatin, which could not have been appreciated without the models of detailed nucleosome assemblies

  • We investigated the crowding effect on the pair interaction between nucleosome clutches as a model of local interaction sites in chromatins, with the aim of understanding the effect of macromolecular crowding on the large-scale chromatin compaction

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Summary

Introduction

Cellular environments are highly crowded with biological macromolecules, such as proteins and RNAs, and it was shown that the change in the degree of macromolecular crowding could significantly influence the structural and dynamic properties of diverse biological processes[1,2,3,4,5]. Computational studies confirmed that the crowding-induced effective attraction could significantly reduce the size of chromatin domains in more crowded environments[13,14]. In these studies, chromatins were modeled as chains of spherical units of several tens of nanometer diameter, representing the local assemblies of DNA and proteins. Our simulation results using the two models of nucleosome clutches revealed that the macromolecular crowding can have distinguishable entropic influences on structural units of euchromatin and heterochromatin, which could not have been appreciated without the models of detailed nucleosome assemblies.

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