Control of mouse cardiac morphogenesis and myogenesis by transcription factor MEF2C

Science. 1997 May 30;276(5317):1404-7. doi: 10.1126/science.276.5317.1404.

Abstract

Members of the myocyte enhancer factor-2 (MEF2) family of MADS (MCM1, agamous, deficiens, serum response factor)-box transcription factors bind an A-T-rich DNA sequence associated with muscle-specific genes. The murine MEF2C gene is expressed in heart precursor cells before formation of the linear heart tube. In mice homozygous for a null mutation of MEF2C, the heart tube did not undergo looping morphogenesis, the future right ventricle did not form, and a subset of cardiac muscle genes was not expressed. The absence of the right ventricular region of the mutant heart correlated with down-regulation of the dHAND gene, which encodes a basic helix-loop-helix transcription factor required for cardiac morphogenesis. Thus, MEF2C is an essential regulator of cardiac myogenesis and right ventricular development.

Publication types

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

MeSH terms

  • Acyltransferases / metabolism
  • Animals
  • Gene Expression Regulation, Developmental
  • Gene Targeting
  • Heart / embryology*
  • Heart Ventricles / cytology
  • Heart Ventricles / embryology
  • In Situ Hybridization
  • MEF2 Transcription Factors
  • Mice
  • Mice, Inbred C57BL
  • Morphogenesis* / genetics
  • Morphogenesis* / physiology
  • Mutagenesis
  • Myocardium / cytology
  • Myogenic Regulatory Factors / genetics
  • Myogenic Regulatory Factors / physiology*
  • Stem Cells

Substances

  • MEF2 Transcription Factors
  • Mef2c protein, mouse
  • Myogenic Regulatory Factors
  • Acyltransferases
  • trehalose mycolyltransferase