Sanford/Burnham Institute for Medical Research, 10901 North Torrey Pines Road, La Jolla, CA 92037-1062, USA.
Exp Cell Res. 2010 Nov 1;316(18):3073-80. doi: 10.1016/j.yexcr.2010.05.023. Epub 2010 May 27.
Skeletal muscle differentiation relies on the coordinated activation and repression of specific subsets of genes. This reflects extensive changes in chromatin architecture, composition of chromatin-associated complexes and histone modifications at the promoter/enhancer elements of skeletal muscle genes. An early, key event in the activation of muscle-specific gene transcription is the disruption of the repressive conformation imposed by nucleosomes, which impede the access of pioneer transcription factors, such as the muscle-specific basic helix-loop-helix (bHLH) factors MyoD and Myf5, to their DNA-binding sites. This review focuses on our current understanding of the role of the SWI/SNF ATP-dependent chromatin-remodeling complex in the activation of the myogenic program, by inducing conformational changes permissive for muscle-gene expression. Recent findings suggest that specific combinations of individual SWI/SNF components can generate sub-complexes with specialized functions that are engaged at sequential stages of muscle-gene activation--e.g., initial displacement of the nucleosome followed by the loading of the complete myogenic transcriptosome that promotes gene transcription. SWI/SNF composition and function is regulated by the exchange of specific variants of structural sub-units. In turn, an exchange of histone variants and related epigenetic modifications might reflect the impact of distinct SWI/SNF complexes on the architecture and activity of target promoter/enhancer elements. Thus, the SWI/SNF complexes should be regarded not just as simple executors of the program imposed by transcription factors, but as multifaceted "readers" and "shapers" of the chromatin/DNA landscape within target muscle genes along the transition from myoblasts to myotubes.
骨骼肌分化依赖于特定基因亚群的协调激活和抑制。这反映了染色质结构、染色质相关复合物组成和启动子/增强子元件处组蛋白修饰的广泛变化。肌肉特异性基因转录激活的早期关键事件是破坏核小体施加的抑制构象,核小体阻碍了先驱转录因子(如肌肉特异性碱性螺旋-环-螺旋 (bHLH) 因子 MyoD 和 Myf5)与其 DNA 结合位点的接触。这篇综述重点介绍了我们目前对 SWI/SNF ATP 依赖性染色质重塑复合物在肌生成程序激活中的作用的理解,通过诱导有利于肌肉基因表达的构象变化来实现。最近的发现表明,特定的 SWI/SNF 组件组合可以产生具有专门功能的亚复合物,这些亚复合物在肌肉基因激活的连续阶段被募集——例如,核小体的初始位移,随后是完整的肌生成转录体的加载,从而促进基因转录。SWI/SNF 的组成和功能受特定结构亚基变体的交换调控。反过来,组蛋白变体和相关表观遗传修饰的交换可能反映了不同的 SWI/SNF 复合物对靶启动子/增强子元件的结构和活性的影响。因此,SWI/SNF 复合物不应仅仅被视为转录因子所施加程序的简单执行者,而应被视为沿着成肌细胞向肌管过渡过程中靶肌肉基因内染色质/DNA 景观的多面“读取器”和“塑造者”。