dMec: a novel Mi-2 chromatin remodelling complex involved in transcriptional repression

EMBO J. 2009 Mar 4;28(5):533-44. doi: 10.1038/emboj.2009.3. Epub 2009 Jan 22.

Abstract

The ATP-dependent chromatin remodeller Mi-2 functions as a transcriptional repressor and contributes to the suppression of cell fates during development in several model organisms. Mi-2 is the ATPase subunit of the conserved Nucleosome Remodeling and Deacetylation (NuRD) complex, and transcriptional repression by Mi-2 is thought to be dependent on its associated histone deacetylase. Here, we have purified a novel dMi-2 complex from Drosophila that is distinct from dNuRD. dMec (dMEP-1 complex) is composed of dMi-2 and dMEP-1. dMec is a nucleosome-stimulated ATPase that is expressed in embryos, larval tissues and adult flies. Surprisingly, dMec is far more abundant than dNuRD and constitutes the major dMi-2-containing complex. Both dNuRD and dMec associate with proneural genes of the achaete-scute complex. However, despite lacking a histone deacetylase subunit, only dMec contributes to the repression of proneural genes. These results reveal an unexpected complexity in the composition and function of Mi-2 complexes.

MeSH terms

  • Adenosine Triphosphatases / metabolism*
  • Animals
  • Autoantigens / metabolism*
  • Cells, Cultured
  • Chromatin Assembly and Disassembly / physiology*
  • Drosophila Proteins / metabolism*
  • Drosophila melanogaster / metabolism*
  • Embryo, Nonmammalian / metabolism
  • Gene Expression Regulation, Developmental
  • Histone Deacetylases / metabolism*
  • Larva / metabolism
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex
  • Protein Subunits / metabolism

Substances

  • Autoantigens
  • Drosophila Proteins
  • Mi-2 protein, Drosophila
  • Protein Subunits
  • Histone Deacetylases
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex
  • Adenosine Triphosphatases