| Literature DB >> 32544095 |
Lin Liu1,2, Chenyun Ding1,2, Tingting Fu1,2, Zhenhua Feng3, Ji-Eun Lee4, Liwei Xiao1,2, Zhisheng Xu1,2, Yujing Yin1,2, Qiqi Guo1,2, Zongchao Sun1,2, Wanping Sun1,2, Yan Mao1,2, Likun Yang1,2, Zheng Zhou1,2, Danxia Zhou1,2, Leilei Xu3, Zezhang Zhu3, Yong Qiu3, Kai Ge4, Zhenji Gan1,2.
Abstract
Skeletal muscle depends on the precise orchestration of contractile and metabolic gene expression programs to direct fiber-type specification and to ensure muscle performance. Exactly how such fiber type-specific patterns of gene expression are established and maintained remains unclear, however. Here, we demonstrate that histone monomethyl transferase MLL4 (KMT2D), an enhancer regulator enriched in slow myofibers, plays a critical role in controlling muscle fiber identity as well as muscle performance. Skeletal muscle-specific ablation of MLL4 in mice resulted in downregulation of the slow oxidative myofiber gene program, decreased numbers of type I myofibers, and diminished mitochondrial respiration, which caused reductions in muscle fatty acid utilization and endurance capacity during exercise. Genome-wide ChIP-Seq and mRNA-Seq analyses revealed that MLL4 directly binds to enhancers and functions as a coactivator of the myocyte enhancer factor 2 (MEF2) to activate transcription of slow oxidative myofiber genes. Importantly, we also found that the MLL4 regulatory circuit is associated with muscle fiber-type remodeling in humans. Thus, our results uncover a pivotal role for MLL4 in specifying structural and metabolic identities of myofibers that govern muscle performance. These findings provide therapeutic opportunities for enhancing muscle fitness to combat a variety of metabolic and muscular diseases.Entities:
Keywords: Epigenetics; Metabolism; Muscle Biology; Skeletal muscle; Transcription
Year: 2020 PMID: 32544095 PMCID: PMC7456251 DOI: 10.1172/JCI136155
Source DB: PubMed Journal: J Clin Invest ISSN: 0021-9738 Impact factor: 14.808