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| 題名: | FoxO6 and PGC-1α form a regulatory loop in myogenic cells |
| 作者: | 陳盛良;Chung, Shih Ying;Huang, Wei Chieh;Su, Ching Wen;Lee, Kuan Wei;Chi, Hsiang Cheng;Lin, Cheng Tao;Chen, Szu-Tah;Huang, Kai Min;Tsai, Mu Shiun;Yu, Hui Peng;Chen, Shen Liang |
| 貢獻者: | 生醫理工學院生命科學系 |
| 日期: | 2013-07-08 |
| 上傳時間: | 2026-04-23 11:12:46 (UTC+8) |
| 出版者: | Portland Press, Ltd.;Portland Press Ltd |
| 摘要: | 摘要： Transcription factors of the FoxO (forkhead box O) family regulate a wide range of cellular physiological processes, including metabolic adaptation and myogenic differentiation. The transcriptional activity of most FoxO members is inhibitory to myogenic differentiation and overexpression of FoxO1 inhibits the development of oxidative type I fibres in vivo. In this study, we found that FoxO6, the last discovered FoxO family member, is expressed ubiquitously in various tissues but with higher expression levels in oxidative tissues, such as brain and oxidative muscles. Both the expression level and promoter activity of FoxO6 were found to be enhanced by PGC-1α (peroxisome-proliferator-activated receptor γ co-activator 1α), thus explained its enriched expression in oxidative tissues. We further demonstrated that FoxO6 represses the expression of PGC-1α via direct binding to an upstream A/T-rich element (AAGATATCAAAACA,−2228–2215) in the PGC-1α promoter. Oxidative low-intensity exercise induced PGC-1α but reduced FoxO6 expression levels in hind leg muscles, and the binding of FoxO6 to PGC-1α promoter was also prevented by exercise. As FoxO6 promoter can be co-activated by PGC-1α and its promoter in turn can be repressed by FoxO6, it suggests that FoxO6 and PGC-1α form a regulatory loop for setting oxidative metabolism level in the skeletal muscle, which can be entrained by exercise.
出版者： Portland Press Ltd
出版日期： 2013-06-01
出處： Bioscience Reports, 2013-06, Vol.33 (3)
識別號： ISSN: 0144-8463
識別號： DOI: 10.1042/bsr20130031 |
| 顯示於類別: | [生命科學系] 期刊論文
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