College of Animal Science and Technology, Northwest A&F University, Yangling, China.
Department of Animal Sciences, Purdue University, West Lafayette, IN, USA.
FASEB J. 2021 Jan;35(1):e21154. doi: 10.1096/fj.202001672R. Epub 2020 Nov 2.
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.
成肌发生包括祖细胞增殖、成肌细胞分化和分化、肌细胞融合和肌管成熟的连续阶段。成肌发生的不同阶段由成肌调节因子和各种下游细胞信号协调和调节。在这里,我们确定磷酸酶孤儿 1(Phospho1)为成肌发生的新成员。在静止卫星细胞的激活、增殖和分化过程中,Phospho1 的表达逐渐增加。Phospho1 的过表达抑制成肌细胞的增殖,但促进其分化和融合。相反,Phospho1 的敲低加速了成肌细胞的增殖,但损害了肌管的形成。此外,Phospho1 的敲低降低了 OXPHO 蛋白水平和线粒体密度,而过表达 Phospho1 则上调 OXPHO 蛋白水平并促进线粒体耗氧量。最后,我们表明 Phospho1 的表达受肌生成素控制,肌生成素结合到 Phospho1 的启动子上调节其转录。这些结果表明 Phospho1 在调节成肌细胞分化和线粒体功能方面发挥着关键作用。