Anand G, Shapiro D N, Dickman P S, Prochownik E V
Department of Pediatrics, Children's Hospital of Pittsburgh, Pennsylvania 15213.
J Clin Invest. 1994 Jan;93(1):5-9. doi: 10.1172/JCI116982.
Skeletal myogenesis is regulated by a group of transcription factors (MyoD, myogenin, myf5, and myf6) that are "basic helix-loop-helix" proteins that bind to the promoters of muscle-specific genes and promote their expression. We have previously shown that after a mutation of Leu122 to Arg the DNA binding basic domain of MyoD confers c-myc-like functional characteristics to the protein. In this study we used single-strand conformation polymorphism analysis to determine whether such mutations occur naturally in rhabdomyosarcomas. We have found that the basic domains of all the myogenic factors remain unaltered in rhabdomyosarcomas. Selection against such mutations may be the result of functional redundancy of these myogenic transcription factors.
骨骼肌生成受一组转录因子(MyoD、肌细胞生成素、Myf5和Myf6)调控,这些转录因子是“碱性螺旋-环-螺旋”蛋白,可与肌肉特异性基因的启动子结合并促进其表达。我们之前已经表明,MyoD的DNA结合碱性结构域在Leu122突变为Arg后赋予该蛋白类似c-myc的功能特性。在本研究中,我们使用单链构象多态性分析来确定此类突变是否在横纹肌肉瘤中自然发生。我们发现,在横纹肌肉瘤中,所有生肌因子的碱性结构域均未改变。对这类突变的选择淘汰可能是这些生肌转录因子功能冗余的结果。