Histone chaperones cooperate to mediate Mef2-targeted transcriptional regulation during skeletal myogenesis

Biochem Biophys Res Commun. 2011 Apr 15;407(3):541-7. doi: 10.1016/j.bbrc.2011.03.055. Epub 2011 Mar 21.

Abstract

Histone chaperones function in histone transfer and regulate the nucleosome occupancy and the activity of genes. HIRA is a replication-independent (RI) histone chaperone that is linked to transcription and various developmental processes. Here, we show that HIRA interacts with Mef2 and contributes to the activation of Mef2-target genes during muscle differentiation. Asf1 cooperated with HIRA and was indispensable for Mef2-dependent transcription. The HIRA R460A mutant, which is defective in Asf1 binding, lost the transcriptional co-activation. In addition, the role of Cabin1, previously reported as a Mef2 repressor and as one of the components of the HIRA-containing complex, was delineated in Mef2/HIRA-mediated transcription. Cabin1 associated with the C-terminus of HIRA via its N-terminal domain and suppressed Mef2/HIRA-mediated transcription. Expression of Cabin1 was dramatically reduced upon myoblast differentiation, which may allow Mef2 and HIRA/Asf1 to resume their transcriptional activity. HIRA led to more permeable chromatin structure marked by active histone modifications around the myogenin promoter. Our results suggest that histone chaperone complex components contribute to the regulation of Mef2 target genes for muscle differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing
  • Animals
  • Calcineurin / metabolism
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Chromatin Immunoprecipitation
  • Chromosomal Proteins, Non-Histone
  • Gene Expression Regulation*
  • Histone Chaperones / genetics
  • Histone Chaperones / metabolism*
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • MEF2 Transcription Factors
  • Mice
  • Muscle Development / genetics*
  • Muscle, Skeletal / growth & development*
  • MyoD Protein / genetics
  • Myogenic Regulatory Factors / genetics
  • Myogenic Regulatory Factors / metabolism*
  • Myogenin / genetics
  • Phosphoproteins / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transcription, Genetic

Substances

  • Adaptor Proteins, Signal Transducing
  • Asf1b protein, mouse
  • Cabin1 protein, mouse
  • Cell Cycle Proteins
  • Chromosomal Proteins, Non-Histone
  • HIRA protein, human
  • Histone Chaperones
  • Intracellular Signaling Peptides and Proteins
  • MEF2 Transcription Factors
  • Mef2a protein, mouse
  • MyoD Protein
  • Myogenic Regulatory Factors
  • Myogenin
  • Phosphoproteins
  • Transcription Factors
  • Calcineurin