Collaborative interactions between MEF-2 and Sp1 in muscle-specific gene regulation

J Cell Biochem. 1998 Sep 1;70(3):366-75.

Abstract

Previous investigations have demonstrated synergistic interactions in vivo between CCAC and A/T-rich nucleotide sequence motifs as functional components of muscle-specific transcriptional enhancers. Using CCAC and A/T-rich elements from the myoglobin and muscle creatine kinase (MCK) gene enhancers, Sp1 and myocyte-specific enhancer factor-2 (MEF-2) were identified as cognate binding proteins that recognize these sites. Physical interactions between Sp1 and MEF-2 were demonstrated by immunological detection of both proteins in DNA binding complexes formed in vitro by nuclear extracts in the presence of only the A/T sequence motif, by coprecipitation of recombinant MEF-2 in the presence of a glutathione-S-transferase-Sp1 fusion protein bound to glutathione beads, and by a two-hybrid assay in Saccharomyces cerevisiae. The interaction with Sp1 in vitro and in vivo is specific for MEF-2 and was not observed with serum response factor, a related MADS domain protein. Forced expression of Sp1 and MEF-2 in insect cells otherwise lacking these factors promotes synergistic transcriptional activation of a promoter containing binding sites for both proteins. These data expand the repertoire of functional and physical interactions between lineage-restricted (MEF-2) and ubiquitous (Sp1) transcription factors that may be important for myogenic differentiation.

Publication types

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

MeSH terms

  • Animals
  • Cell Line
  • Creatine Kinase / genetics*
  • DNA-Binding Proteins / metabolism*
  • Drosophila Proteins
  • Drosophila melanogaster
  • Enhancer Elements, Genetic
  • Gene Expression Regulation*
  • Glutathione Transferase
  • Luciferases
  • MEF2 Transcription Factors
  • Mice
  • Muscles / metabolism*
  • Myogenic Regulatory Factors
  • Myoglobin / genetics
  • Nuclear Proteins / metabolism
  • Organ Specificity
  • Protein Biosynthesis
  • Recombinant Fusion Proteins / isolation & purification
  • Recombinant Fusion Proteins / metabolism
  • Saccharomyces cerevisiae / genetics
  • Serum Response Factor
  • Sp1 Transcription Factor / metabolism*
  • Transcription Factors / metabolism*
  • Transfection

Substances

  • DNA-Binding Proteins
  • Drosophila Proteins
  • MEF2 Transcription Factors
  • Mef2 protein, Drosophila
  • Myogenic Regulatory Factors
  • Myoglobin
  • Nuclear Proteins
  • Recombinant Fusion Proteins
  • Serum Response Factor
  • Sp1 Transcription Factor
  • Transcription Factors
  • Luciferases
  • Glutathione Transferase
  • Creatine Kinase