Padilla-Benavides Teresita, Reyes-Gutierrez Pablo, Imbalzano Anthony N
Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA 01605, USA.
Department of Molecular Biology and Biochemistry, Wesleyan University, Middletown, CT 06459, USA.
Biology (Basel). 2020 Jul 3;9(7):152. doi: 10.3390/biology9070152.
Myogenesis is the biological process by which skeletal muscle tissue forms. Regulation of myogenesis involves a variety of conventional, epigenetic, and epigenomic mechanisms that control chromatin remodeling, DNA methylation, histone modification, and activation of transcription factors. Chromatin remodeling enzymes utilize ATP hydrolysis to alter nucleosome structure and/or positioning. The mammalian SWItch/Sucrose Non-Fermentable (mSWI/SNF) family of chromatin remodeling enzymes is essential for myogenesis. Here we review diverse and novel mechanisms of regulation of mSWI/SNF enzymes by kinases and phosphatases. The integration of classic signaling pathways with chromatin remodeling enzyme function impacts myoblast viability and proliferation as well as differentiation. Regulated processes include the assembly of the mSWI/SNF enzyme complex, choice of subunits to be incorporated into the complex, and sub-nuclear localization of enzyme subunits. Together these processes influence the chromatin remodeling and gene expression events that control myoblast function and the induction of tissue-specific genes during differentiation.
肌生成是骨骼肌组织形成的生物学过程。肌生成的调控涉及多种传统、表观遗传和表观基因组机制,这些机制控制染色质重塑、DNA甲基化、组蛋白修饰以及转录因子的激活。染色质重塑酶利用ATP水解来改变核小体结构和/或定位。哺乳动物染色质重塑酶的SWItch/蔗糖非发酵(mSWI/SNF)家族对肌生成至关重要。在此,我们综述激酶和磷酸酶对mSWI/SNF酶调控的多种新机制。经典信号通路与染色质重塑酶功能的整合影响成肌细胞的活力、增殖以及分化。受调控的过程包括mSWI/SNF酶复合物的组装、纳入复合物的亚基选择以及酶亚基的核内定位。这些过程共同影响染色质重塑和基因表达事件,从而控制成肌细胞功能以及分化过程中组织特异性基因的诱导。