Laker Rhianna C, Ryall James G
Department of Medicine, Center for Skeletal Muscle Research at the Robert M. Berne Cardiovascular Research Center, University of Virginia, Charlottesville, VA 22908, USA.
Stem Cell Metabolism & Regenerative Medicine Group, Basic & Clinical Myology Laboratory, The University of Melbourne, Melbourne, VIC 3010, Australia.
Stem Cells Int. 2016;2016:5725927. doi: 10.1155/2016/5725927. Epub 2016 Jan 5.
An unresolved and critically important question in skeletal muscle biology is how muscle stem cells initiate and regulate the genetic program during muscle development. Epigenetic dynamics are essential for cellular development and organogenesis in early life and it is becoming increasingly clear that epigenetic remodeling may also be responsible for the cellular adaptations that occur in later life. DNA methylation of cytosine bases within CpG dinucleotide pairs is an important epigenetic modification that reduces gene expression when located within a promoter or enhancer region. Recent advances in the field suggest that epigenetic regulation is essential for skeletal muscle stem cell identity and subsequent cell development. This review summarizes what is currently known about how skeletal muscle stem cells regulate the myogenic program through DNA methylation, discusses a novel role for metabolism in this process, and addresses DNA methylation dynamics in adult skeletal muscle in response to physical activity.
骨骼肌生物学中一个尚未解决且至关重要的问题是,肌肉干细胞如何在肌肉发育过程中启动和调节基因程序。表观遗传动力学对于生命早期的细胞发育和器官形成至关重要,并且越来越清楚的是,表观遗传重塑也可能是后期生命中发生的细胞适应性变化的原因。位于CpG二核苷酸对中的胞嘧啶碱基的DNA甲基化是一种重要的表观遗传修饰,当位于启动子或增强子区域时会降低基因表达。该领域的最新进展表明,表观遗传调控对于骨骼肌干细胞的特性及随后的细胞发育至关重要。本综述总结了目前关于骨骼肌干细胞如何通过DNA甲基化调节肌生成程序的已知信息,讨论了代谢在此过程中的新作用,并探讨了成年骨骼肌对体育活动作出反应时的DNA甲基化动态变化。