hMusTRD1alpha1 represses MEF2 activation of the troponin I slow enhancer

J Biol Chem. 2003 Sep 19;278(38):36603-10. doi: 10.1074/jbc.M212814200. Epub 2003 Jul 10.

Abstract

The novel transcription factor hMusTRD1alpha1 (human muscle TFII-I repeat domain-containing protein 1alpha1; previously named MusTRD1; O'Mahoney, J. V., Guven, K. L., Lin, J., Joya, J. E., Robinson, C. S., Wade, R. P., and Hardeman, E. C. (1998) Mol. Cell. Biol. 18, 6641-6652) was identified in a yeast one-hybrid screen as a protein that binds within an upstream enhancer-containing region of the skeletal muscle-specific gene, TNNI1 (human troponin I slow; hTnIslow). It has been proposed that hMusTRD1alpha1 may play an important role in fiber-specific muscle gene expression by virtue of its ability to bind to an Inr-like element (nucleotides -977 to -960) within the hTnIslow upstream enhancer-containing region that is necessary for slow fiber-specific expression. In this study we demonstrate that both MEF2C, a known regulator of slow fiber-specific genes, and hMusTRD1alpha1 regulate hTnIslow through the Inr-like element. Co-transfection assays in C2C12 cells and Cos-7 cells demonstrate that hMusTRD1alpha1 represses hTnIslow transcription and prevents MEF2C-mediated activation of hTnIslow transcription. Gel shift analysis shows that hMusTRD1alpha1 can abrogate MEF2C binding to its cognate site in the hTnIslow enhancer. Glutathione S-transferase pull-down assays demonstrate that hMusTRD1alpha1 can interact with both MEF2C and the nuclear receptor co-repressor. The data support the role of hMusTRD1alpha1 as a repressor of slow fiber-specific transcription through mechanisms involving direct interactions with MEF2C and the nuclear receptor co-repressor.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • COS Cells
  • Cell Line
  • Cell Nucleus / metabolism
  • DNA / metabolism
  • DNA-Binding Proteins / chemistry*
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism*
  • Gene Expression Regulation
  • Glutathione Transferase / metabolism
  • MEF2 Transcription Factors
  • Mice
  • Models, Biological
  • Models, Genetic
  • Muscle Fibers, Slow-Twitch / metabolism
  • Muscle Proteins*
  • Muscle, Skeletal / metabolism
  • Myogenic Regulatory Factors
  • Nuclear Proteins*
  • Plasmids / metabolism
  • Precipitin Tests
  • Protein Binding
  • Protein Structure, Tertiary
  • Repressor Proteins / chemistry*
  • Repressor Proteins / genetics*
  • Reverse Transcriptase Polymerase Chain Reaction
  • Trans-Activators*
  • Transcription Factors / metabolism*
  • Transcription, Genetic
  • Transcriptional Activation
  • Troponin I / chemistry*
  • Two-Hybrid System Techniques

Substances

  • DNA-Binding Proteins
  • Gtf2ird1 protein, mouse
  • MEF2 Transcription Factors
  • Mef2c protein, mouse
  • Muscle Proteins
  • Myogenic Regulatory Factors
  • Nuclear Proteins
  • Repressor Proteins
  • Trans-Activators
  • Transcription Factors
  • Troponin I
  • DNA
  • Glutathione Transferase