| Literature DB >> 33140469 |
Ying Peng1,2, Feng Yue2, Jingjuan Chen2, Wei Xia2,3, Kuilong Huang1,2, Gongshe Yang1, Shihuan Kuang2.
Abstract
Myogenesis includes sequential stages of progenitor cell proliferation, myogenic commitment and differentiation, myocyte fusion, and myotube maturation. Different stages of myogenesis are orchestrated and regulated by myogenic regulatory factors and various downstream cellular signaling. Here we identify phosphatase orphan 1 (Phospho1) as a new player in myogenesis. During activation, proliferation, and differentiation of quiescent satellite cells, the expression of Phospho1 gradually increases. Overexpression of Phospho1 inhibits myoblast proliferation but promotes their differentiation and fusion. Conversely, knockdown of Phospho1 accelerates myoblast proliferation but impairs myotube formation. Moreover, knockdown of Phospho1 decreases the OXPHO protein levels and mitochondria density, whereas overexpression of Phospho1 upregulates OXPHO protein levels and promotes mitochondrial oxygen consumption. Finally, we show that Phospho1 expression is controlled by myogenin, which binds to the promoter of Phospho1 to regulate its transcription. These results indicate a key role of Phospho1 in regulating myogenic differentiation and mitochondrial function.Entities:
Keywords: MyoG; Phospho1; mitochondria; myogenesis
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Year: 2020 PMID: 33140469 PMCID: PMC7983050 DOI: 10.1096/fj.202001672R
Source DB: PubMed Journal: FASEB J ISSN: 0892-6638 Impact factor: 5.191