RDF/XMLNTriplesTurtleShow queryShare
SubjectPredicateObject
http://purl.uniprot.org/citations/27506764http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/27506764http://www.w3.org/2000/01/rdf-schema#comment"Upon adaption of skeletal muscle to physiological and pathophysiological stimuli, muscle fiber type and mitochondrial function are coordinately regulated. Recent studies have identified pathways involved in control of contractile proteins of oxidative-type fibers. However, the mechanism for coupling of mitochondrial function to the muscle contractile machinery during fiber type transition remains unknown. Here, we show that the expression of the genes encoding type I myosins, Myh7/Myh7b and their intronic miR-208b/miR-499, parallels mitochondrial function during fiber type transitions. Using in vivo approaches in mice, we found that miR-499 drives a PGC-1α-dependent mitochondrial oxidative metabolism program to match shifts in slow-twitch muscle fiber composition. Mechanistically, miR-499 directly targets Fnip1, an AMP-activated protein kinase (AMPK)-interacting protein that negatively regulates AMPK, a known activator of PGC-1α. Inhibition of Fnip1 reactivated AMPK/PGC-1α signaling and mitochondrial function in myocytes. Restoration of the expression of miR-499 in the mdx mouse model of Duchenne muscular dystrophy (DMD) reduced the severity of DMD Thus, we have identified a miR-499/Fnip1/AMPK circuit that can serve as a mechanism to couple muscle fiber type and mitochondrial function."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.org/dc/terms/identifier"doi:10.15252/emmm.201606372"xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Gao X."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Liu J."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Liang X."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Liu L."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Kelly D.P."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Xiao L."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Zhou Q."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Zhou D."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Kong Y."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Vega R.B."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Lai L."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Fu T."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Gan Z."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/author"Zhu M.S."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/date"2016"xsd:gYear
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/name"EMBO Mol Med"xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/pages"1212-1228"xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/title"Coupling of mitochondrial function and skeletal muscle fiber type by a miR-499/Fnip1/AMPK circuit."xsd:string
http://purl.uniprot.org/citations/27506764http://purl.uniprot.org/core/volume"8"xsd:string
http://purl.uniprot.org/citations/27506764http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/27506764
http://purl.uniprot.org/citations/27506764http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/27506764
http://purl.uniprot.org/uniprot/#_A0A0G2JGG3-mappedCitation-27506764http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/27506764