Abstract

BackgroundThe activity of a single gene is influenced by the composition of the chromatin in which it is embedded. Nucleosome turnover, conformational dynamics, and covalent histone modifications each induce changes in the structure of chromatin and its affinity for regulatory proteins. The dynamics of histone modifications and the persistence of modification patterns for long periods are still largely unknown.ResultsIn this study, we present a stochastic mathematical model that describes the molecular mechanisms of histone modification pattern formation along a single gene, with non-phenomenological, physical parameters. We find that diffusion and recruitment properties of histone modifying enzymes together with chromatin connectivity allow for a rich repertoire of stochastic histone modification dynamics and pattern formation. We demonstrate that histone modification patterns at a single gene can be established or removed within a few minutes through diffusion and weak recruitment mechanisms of histone modification spreading. Moreover, we show that strong synergism between diffusion and weak recruitment mechanisms leads to nearly irreversible transitions in histone modification patterns providing stable patterns. In the absence of chromatin connectivity spontaneous and dynamic histone modification boundaries can be formed that are highly unstable, and spontaneous fluctuations cause them to diffuse randomly. Chromatin connectivity destabilizes this synergistic system and introduces bistability, illustrating state switching between opposing modification states of the model gene. The observed bistable long-range and localized pattern formation are critical effectors of gene expression regulation.ConclusionThis study illustrates how the cooperative interactions between regulatory proteins and the chromatin state generate complex stochastic dynamics of gene expression regulation.Electronic supplementary materialThe online version of this article (doi:10.1186/1756-8935-7-30) contains supplementary material, which is available to authorized users.

Highlights

  • The activity of a single gene is influenced by the composition of the chromatin in which it is embedded

  • The histone modification spreading model We consider a nucleosomal chromatin region of 10 kb corresponding to the length of an average human gene (Figure 1A)

  • In this study we present a stochastic mathematical model that describes the mechanisms of histone modification spreading

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Summary

Introduction

The activity of a single gene is influenced by the composition of the chromatin in which it is embedded. Nucleosome turnover, conformational dynamics, and covalent histone modifications each induce changes in the structure of chromatin and its affinity for regulatory proteins. Chromatin folding into higher-order structures, and binding of large regulatory protein assemblies to the chromatin play a critical role in generating the epigenetic state. Changes in chromatin structure are guided by post-translational covalent histone modifications. A prominent feature of core histones is the large amount and diversity of covalently modified residues they can possess [2,15]. These marks guide the recruitment and binding of defined histone modifying enzymes and other regulatory proteins [16]. All of the above mentioned processes play a key role in regulation of transcription at the level of single genes [19,20,21,22]

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