| Literature DB >> 35733026 |
Govind Menon1, Martin Howard2.
Abstract
The maintenance of transcriptional states regulated by histone modifications and controlled switching between these states are fundamental concepts in our understanding of nucleosome-mediated epigenetic memory. Any approach relying on genome-wide bioinformatic analyses alone offers limited scope for dissecting the molecular mechanisms involved in maintenance and switching. Mechanistic mathematical models-describing the dynamics of histone modifications at individual genomic loci-offer an alternative way to investigate these mechanisms. These models, in conjunction with quantitative experimental data-ChIP data, quantification of mRNA levels, and single-cell fluorescence tracking in clonal lineages-can generate predictions that drive more targeted experiments, allowing us to understand mechanisms that would be challenging to unravel by a purely experimental approach. In this chapter, we describe a generic stochastic modeling framework that can be used to capture histone modification dynamics and associated molecular processes-including transcription and read-write feedback by chromatin modifying complexes-at individual genomic loci. Using a specific example-transcriptional silencing by Polycomb-mediated H3K27 methylation-we demonstrate how to construct and simulate a stochastic histone modification model. We provide a step-by-step guide to programming simulations for such a model and discuss how to analyze the simulation output.Entities:
Keywords: Bistability; Gene expression states; Gillespie algorithm; Maintenance and switching; Mechanistic modeling; Nucleosome-mediated epigenetic memory; Polycomb; Stochastic histone modification model
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Year: 2022 PMID: 35733026 DOI: 10.1007/978-1-0716-2481-4_19
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745