Control of Mouse Cardiac Morphogenesis and Myogenesis by Transcription Factor MEF2C

Author:

Lin Qing123,Schwarz John123,Bucana Corazon123,N. Olson Eric123

Affiliation:

1. Q. Lin and E. N. Olson, Department of Molecular Biology and Oncology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75235–9148, USA.

2. J. Schwarz, Division of Cardiology, Department of Internal Medicine, University of Texas Medical School, Houston, TX 77030, USA.

3. C. Bucana, Department of Cell Biology, University of Texas M. D. Anderson Cancer Center, Houston, TX 77030, USA.

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.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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