Lu J, Webb R, Richardson J A, Olson E N
Department of Molecular Biology and Oncology, University of Texas Southwestern Medical Center, 6000 Harry Hines Boulevard, Dallas, TX 75235-9148, USA.
Proc Natl Acad Sci U S A. 1999 Jan 19;96(2):552-7. doi: 10.1073/pnas.96.2.552.
Skeletal muscle development is controlled by a family of muscle-specific basic helix-loop-helix (bHLH) transcription factors that activate muscle genes by binding E-boxes (CANNTG) as heterodimers with ubiquitous bHLH proteins, called E proteins. Myogenic bHLH factors are expressed in proliferating undifferentiated myoblasts, but they do not initiate myogenesis until myoblasts exit the cell cycle. We describe a bHLH protein, MyoR (for myogenic repressor), that is expressed in undifferentiated myoblasts in culture and is down-regulated during differentiation. MyoR is also expressed specifically in the skeletal muscle lineage between days 10.5 and 16.5 of mouse embryogenesis and down-regulated thereafter during the period of secondary myogenesis. MyoR forms heterodimers with E proteins that bind the same DNA sequence as myogenic bHLH/E protein heterodimers, but MyoR acts as a potent transcriptional repressor that blocks myogenesis and activation of E-box-dependent muscle genes. These results suggest a role for MyoR as a lineage-restricted transcriptional repressor of the muscle differentiation program.
骨骼肌发育受一类肌肉特异性碱性螺旋-环-螺旋(bHLH)转录因子控制,这些转录因子作为异二聚体与名为E蛋白的普遍存在的bHLH蛋白结合E盒(CANNTG),从而激活肌肉基因。生肌bHLH因子在增殖的未分化成肌细胞中表达,但直到成肌细胞退出细胞周期,它们才启动肌生成。我们描述了一种bHLH蛋白,即MyoR(生肌抑制因子),它在培养的未分化成肌细胞中表达,在分化过程中下调。MyoR在小鼠胚胎发育第10.5天至16.5天之间的骨骼肌谱系中也特异性表达,此后在次级肌生成期间下调。MyoR与E蛋白形成异二聚体,其结合的DNA序列与生肌bHLH/E蛋白异二聚体相同,但MyoR作为一种有效的转录抑制因子,可阻断肌生成和E盒依赖性肌肉基因的激活。这些结果表明MyoR作为肌肉分化程序的谱系限制性转录抑制因子发挥作用。