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肌肉生长抑制素通过PI3K/PTEN/Akt信号通路诱导p300降解,从而使细胞周期蛋白D1表达沉默。

Myostatin induces p300 degradation to silence cyclin D1 expression through the PI3K/PTEN/Akt pathway.

作者信息

Ji Ming, Zhang Qiang, Ye Jianwei, Wang Xueyan, Yang Wei, Zhu Dahai

机构信息

National Laboratory of Medical Molecular Biology and Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences and Peking Union Medical College, Tsinghua University, 5 Dong Dan San Tiao, Beijing 100005, PR China.

出版信息

Cell Signal. 2008 Aug;20(8):1452-8. doi: 10.1016/j.cellsig.2008.03.013. Epub 2008 Apr 1.

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.

摘要

肌生成抑制素是骨骼肌生长的负调节因子,影响众多参与细胞增殖、分化和代谢的基因表达。然而,肌生成抑制素调节基因表达的分子机制仍有待阐明。在本研究中,我们发现肌生成抑制素阻止p300募集到细胞周期蛋白D1启动子,导致细胞周期蛋白D1表达沉默。我们的数据进一步表明,肌生成抑制素通过泛素-蛋白酶体系统诱导p300降解,从而降低p300的蛋白水平。此外,我们提供的实验证据表明,肌生成抑制素诱导的p300降解由磷脂酰肌醇3-激酶/PTEN/Akt信号通路介导,而IGF-1或胰岛素可拮抗这一过程。本研究结果揭示了对肌生成抑制素响应的基因表达的表观遗传调控。

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