Department of Biochemistry and Molecular Genetics, University of Virginia, 1300 Jefferson Park Ave, Jordan Hall 1240, University of Virginia School of Medicine, Charlottesville, VA 22908, United States.
Curr Opin Pharmacol. 2012 Jun;12(3):383-8. doi: 10.1016/j.coph.2012.02.001. Epub 2012 Mar 2.
The genetics of skeletal muscle lineage commitment are deceptively complicated. MyoD overexpression is sufficient to convert fibroblasts into skeletal muscle myotubes. In vivo, there are a number of different steps of differentiation that require a large network of transcription factors that control differentiation and homeostasis of skeletal muscle progenitors. Each transcription factor has been shown to have the ability to promote the next factor in the cascade, but the mechanisms regulating the transitions remain incomplete. Recently, microRNAs have been shown to be important for a large number of developmental and oncogenic processes. In this review, we will discuss recent advances in the understanding of how microRNA is critical for skeletal muscle development by interacting with protein-coding genes that had previously been shown to be important for myogenesis.
骨骼肌谱系决定的遗传学非常复杂。MyoD 的过表达足以将成纤维细胞转化为骨骼肌肌管。在体内,有许多不同的分化步骤需要一个大型转录因子网络来控制骨骼肌祖细胞的分化和稳态。已经表明每个转录因子都有能力促进级联中的下一个因子,但调节这些转变的机制仍不完整。最近,microRNA 已被证明在许多发育和致癌过程中非常重要。在这篇综述中,我们将讨论最近在理解 microRNA 通过与先前显示对肌发生重要的蛋白质编码基因相互作用从而对骨骼肌发育至关重要方面的进展。