Bottom-up modeling of chromatin segregation due to epigenetic modifications

Proc Natl Acad Sci U S A. 2018 Dec 11;115(50):12739-12744. doi: 10.1073/pnas.1812268115. Epub 2018 Nov 26.

Abstract

We use a chromosome-scale simulation to show that the preferential binding of heterochromatin protein 1 (HP1) to regions high in histone methylation (specifically H3K9me3) results in phase segregation and reproduces features of the observed Hi-C contact map. Specifically, we perform Monte Carlo simulations with one computational bead per nucleosome and an H3K9me3 pattern based on published ChIP-seq signals. We implement a binding model in which HP1 preferentially binds to trimethylated histone tails and then oligomerizes to bridge together nucleosomes. We observe a phase reminiscent of heterochromatin-dense and high in H3K9me3-and another reminiscent of euchromatin-less dense and lacking H3K9me3. This segregation results in a plaid contact probability map that matches the general shape and position of published Hi-C data. Analysis suggests that a roughly 20-kb segment of H3K9me3 enrichment is required to drive segregation into the heterochromatic phase.

Keywords: Hi-C; chromosomal organization; epigenetic regulation; genomic architecture; polymer simulation.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Chromatin / genetics*
  • Chromobox Protein Homolog 5
  • Chromosomal Proteins, Non-Histone / genetics
  • Chromosome Segregation / genetics*
  • Epigenesis, Genetic / genetics*
  • Euchromatin / genetics
  • Heterochromatin / genetics
  • Histones / genetics
  • Humans
  • Monte Carlo Method
  • Nucleosomes / genetics
  • Probability

Substances

  • Chromatin
  • Chromosomal Proteins, Non-Histone
  • Euchromatin
  • Heterochromatin
  • Histones
  • Nucleosomes
  • Chromobox Protein Homolog 5