Perspective on unraveling the versatility of 'co-repressor' complexes

Biochim Biophys Acta. 2015 Aug;1849(8):1051-6. doi: 10.1016/j.bbagrm.2015.06.012. Epub 2015 Jun 28.

Abstract

A multitude of post-translational modifications take place on histones, one of the best studied being acetylation on lysine residues, which is generally associated with gene activation. During the last decades, several so-called co-repressor protein complexes that carry out the reverse process, histone deacetylation, have been identified and characterized, such as the Sin3, N-CoR/SMRT and NuRD complexes. Although a repressive role for these complexes in regulating gene expression is well established, accumulating evidence also points to a role in gene activation. Here, we argue that integration of various state-of-the-art technologies, addressing different aspects of transcriptional regulation, is essential to unravel this apparent biological versatility of 'co-repressor' complexes.

Keywords: Co-repressor complexes; Gene regulation; Histone deacetylation; Technology integration.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Co-Repressor Proteins / physiology*
  • Gene Expression Regulation*
  • Humans
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex / physiology
  • Multiprotein Complexes / physiology*
  • Nuclear Receptor Co-Repressor 1 / physiology
  • Nuclear Receptor Co-Repressor 2 / physiology
  • Transcription Factors / physiology*

Substances

  • Co-Repressor Proteins
  • Multiprotein Complexes
  • NCOR1 protein, human
  • Nuclear Receptor Co-Repressor 1
  • Nuclear Receptor Co-Repressor 2
  • Transcription Factors
  • Mi-2 Nucleosome Remodeling and Deacetylase Complex