Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10816999 | Cellular Signalling | 2008 | 7 Pages |
Abstract
Myostatin is a negative regulator of skeletal muscle growth and affects numerous genes expression involved in cell proliferation, differentiation and metabolism. However, the molecular mechanisms underlying myostatin-regulated genes expression remain to be elucidated. In this study, we showed that myostatin blocked the recruitment of p300 to the cyclin D1 promoter, resulting in the silence of cyclin D1 expression. Our data further demonstrated that myostatin decreased the protein level of p300 by inducing p300 degradation via the ubiquitin-proteasome system. In addition, we provided experimental evidence to show that myostatin-induced p300 degradation was mediated by the phosphatidylinositol 3-kinase/PTEN/Akt signaling pathway and this could be antagonized by IGF-1 or insulin. Results presented in this study uncovered an epigenetic control of genes expression in response to myostatin.
Keywords
PI3KTGF-βMSTNP300IGF-1ERKHDACsJnkc-Jun N-terminal kinaseMAPKAktHistone acetylationinsulin-like growth factor-1transforming growth factor-βphosphatase and tensin homolog deleted on chromosome 10Phosphatidylinositol 3-kinaseMyostatinhistone deacetylaseshistone acetyltransferasesmitogen-activated protein kinasePtenHATs
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Authors
Ming Ji, Qiang Zhang, Jianwei Ye, Xueyan Wang, Wei Yang, Dahai Zhu,