The Nucleosome Remodeling and Deacetylation Complex Modulates Chromatin Structure at Sites of Active Transcription to Fine-Tune Gene Expression

Mol Cell. 2018 Jul 5;71(1):56-72.e4. doi: 10.1016/j.molcel.2018.06.003. Epub 2018 Jun 28.

Abstract

Chromatin remodeling complexes play essential roles in metazoan development through widespread control of gene expression, but the precise molecular mechanisms by which they do this in vivo remain ill defined. Using an inducible system with fine temporal resolution, we show that the nucleosome remodeling and deacetylation (NuRD) complex controls chromatin architecture and the protein binding repertoire at regulatory regions during cell state transitions. This is primarily exerted through its nucleosome remodeling activity while deacetylation at H3K27 follows changes in gene expression. Additionally, NuRD activity influences association of RNA polymerase II at transcription start sites and subsequent nascent transcript production, thereby guiding the establishment of lineage-appropriate transcriptional programs. These findings provide a detailed molecular picture of genome-wide modulation of lineage-specific transcription by an essential chromatin remodeling complex as well as insight into the orchestration of molecular events involved in transcriptional transitions in vivo. VIDEO ABSTRACT.

Keywords: Mediator; NuRD; RNA polymerase II; chromatin; embryonic stem cells; enhancer; transcription; transcription factor.

Publication types

  • Research Support, Non-U.S. Gov't
  • Video-Audio Media

MeSH terms

  • Acetylation
  • Animals
  • Cell Line
  • Gene Expression Regulation*
  • Histones / genetics
  • Histones / metabolism
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex / genetics
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex / metabolism*
  • Mice
  • Mouse Embryonic Stem Cells / cytology
  • Mouse Embryonic Stem Cells / metabolism*
  • Nucleosomes / genetics
  • Nucleosomes / metabolism*
  • RNA Polymerase II / genetics
  • RNA Polymerase II / metabolism*
  • Transcription Initiation Site
  • Transcription, Genetic*

Substances

  • Histones
  • Nucleosomes
  • RNA Polymerase II
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex