Lin Q, Schwarz J, Bucana C, Olson E N
Department of Molecular Biology and Oncology, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75235-9148, USA.
Science. 1997 May 30;276(5317):1404-7. doi: 10.1126/science.276.5317.1404.
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.
MADS(MCM1、无配子生殖、缺失、血清反应因子)盒转录因子的肌细胞增强因子2(MEF2)家族成员可结合与肌肉特异性基因相关的富含A-T的DNA序列。小鼠MEF2C基因在心脏前体细胞中在线性心管形成之前就已表达。在MEF2C基因无效突变的纯合小鼠中,心管未发生环状形态发生,未来的右心室未形成,并且一部分心肌基因未表达。突变心脏右心室区域的缺失与dHAND基因的下调相关,该基因编码心脏形态发生所需的一种碱性螺旋-环-螺旋转录因子。因此,MEF2C是心肌生成和右心室发育的重要调节因子。