O-GlcNAcylation of BMAL1 regulates circadian rhythms in NIH3T3 fibroblasts.

O-GlcNAcylation of BMAL1 regulates circadian rhythms in NIH3T3 fibroblasts.
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BMAL1 的 O-GlcNAc 酰化调节 NIH3T3 成纤维细胞的昼夜节律。

DOI:
10.1016/j.bbrc.2013.01.043
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发表时间:
2013-02
期刊:
Biochem Biophys Res Commun
影响因子:
--
通讯作者:
Li, Jia-Da
Li, Jia-Da
中科院分区:
其他
文献类型:
--
作者:
Ma, Yan-Tao;Luo, Hunjin;Guan, Wen-Juan;Zhang, Hua;Chen, Chongfen;Wang, Ziyao;Li, Jia-Da

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各种生理过程和行为表现出大约24小时的昼夜节律,这在协调体内代谢过程和环境信号方面是至关重要的。翻译后修饰在调节昼夜节律核心蛋白方面起着重要作用。在这项研究中,我们证明了用O-连接的β-N-乙酰氨基葡萄糖(O-GlcNAc)修饰BMAL1,可以稳定BMAL1并增强其转录活性。相反,抑制O-GlcN酰化导致时钟基因表达的昼夜节律被抑制。由于O-GlcN酰化对葡萄糖水平很敏感,这种修饰可能会提供一种新的机制,将代谢与昼夜节律联系起来。
Various physiological processes and behaviors show a circadian rhythm of approximately 24h, which is crucial in coordinating internal metabolic processes and environmental signals. Post-translational modifications play an important role in regulating circadian core proteins. In this study, we demonstrated that BMAL1 was modified with an O-linked β-N-acetylglucosamine (O-GlcNAc), which stabilized BMAL1 and enhanced its transcriptional activity. Conversely, inhibition of O-GlcNAcylation resulted in inhibition of circadian rhythms of clock gene expression. Because O-GlcNAcylation is sensitive to the glucose level, such a modification may provide a new mechanism connecting metabolism with circadian rhythms.
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