Delayed Accumulation of H3K27me3 on Nascent DNA Is Essential for Recruitment of Transcription Factors at Early Stages of Stem Cell Differentiation

Mol Cell. 2017 Apr 20;66(2):247-257.e5. doi: 10.1016/j.molcel.2017.03.006. Epub 2017 Apr 11.

Abstract

Recruitment of transcription factors (TFs) to repressed genes in euchromatin is essential to activate new transcriptional programs during cell differentiation. However, recruitment of all TFs, including pioneer factors, is impeded by condensed H3K27me3-containing chromatin. Single-cell and gene-specific analyses revealed that, during the first hours of induction of differentiation of mammalian embryonic stem cells (ESCs), accumulation of the repressive histone mark H3K27me3 is delayed after DNA replication, indicative of a decondensed chromatin structure in all regions of the replicating genome. This delay provides a critical "window of opportunity" for recruitment of lineage-specific TFs to DNA. Increasing the levels of post-replicative H3K27me3 or preventing S phase entry inhibited recruitment of new TFs to DNA and significantly blocked cell differentiation. These findings suggest that recruitment of lineage-specifying TFs occurs soon after replication and is facilitated by a decondensed chromatin structure. This insight may explain the developmental plasticity of stem cells and facilitate their exploitation for therapeutic purposes.

Keywords: DNA replication; H3K27me3; HMTs; KDMs; embryonic stem cells; nascent DNA; nascent chromatin; neuronal differentiation; transcription factors.

MeSH terms

  • Animals
  • Binding Sites
  • Cell Differentiation*
  • Cell Lineage*
  • Cell Plasticity
  • Chromatin / chemistry
  • Chromatin / metabolism*
  • Chromatin Assembly and Disassembly*
  • DNA / biosynthesis*
  • DNA / chemistry
  • DNA / genetics
  • DNA Methylation
  • DNA Replication*
  • Embryonic Stem Cells / metabolism*
  • Gene Expression Regulation, Developmental
  • Histone Demethylases / metabolism
  • Histones / chemistry
  • Histones / metabolism*
  • Humans
  • Methylation
  • Mice
  • Nuclear Proteins / metabolism
  • Nucleic Acid Conformation
  • Protein Binding
  • Structure-Activity Relationship
  • Time Factors
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription, Genetic*

Substances

  • Chromatin
  • Histones
  • Nuclear Proteins
  • Transcription Factors
  • DNA
  • Histone Demethylases
  • KDM6A protein, human