核心
心肌细胞
细胞生物学
生物
基因
计算生物学
基因表达调控
遗传学
作者
Matthieu Dos Santos,Akansha M. Shah,Yichi Zhang,Svetlana Bezprozvannaya,Kenian Chen,Lin Xu,Weichun Lin,John McAnally,Rhonda Bassel‐Duby,Ning Liu,Eric N. Olson
标识
DOI:10.1038/s41467-023-40073-8
摘要
Abstract Skeletal muscle fibers express distinct gene programs during development and maturation, but the underlying gene regulatory networks that confer stage-specific myofiber properties remain unknown. To decipher these distinctive gene programs and how they respond to neural activity, we generated a combined multi-omic single-nucleus RNA-seq and ATAC-seq atlas of mouse skeletal muscle development at multiple stages of embryonic, fetal, and postnatal life. We found that Myogenin, Klf5, and Tead4 form a transcriptional complex that synergistically activates the expression of muscle genes in developing myofibers. During myofiber maturation, the transcription factor Maf acts as a transcriptional switch to activate the mature fast muscle gene program. In skeletal muscles of mutant mice lacking voltage-gated L-type Ca 2+ channels (Cav1.1), Maf expression and myofiber maturation are impaired. These findings provide a transcriptional atlas of muscle development and reveal genetic links between myofiber formation, maturation, and contraction.
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