Kon Naohiro, Hirota Tsuyoshi, Kawamoto Takeshi, Kato Yukio, Tsubota Tadashi, Fukada Yoshitaka
Department of Biophysics and Biochemistry, Graduate School of Science, The University of Tokyo, Hongo 7-3-1, Bunkyo-ku, Tokyo 113-0033, Japan.
Nat Cell Biol. 2008 Dec;10(12):1463-9. doi: 10.1038/ncb1806. Epub 2008 Nov 23.
The circadian clock is reset by external time cues for synchronization to environmental changes. In mammals, the light-input signalling pathway mediated by Per gene induction has been extensively studied. On the other hand, little is known about resetting mechanisms that are independent of Per induction. Here we show that activation of activin receptor-like kinase (ALK), triggered by TGF-beta, activin or alkali signals, evoked resetting of the cellular clock independently of Per induction. The resetting was mediated by an immediate-early induction of Dec1, a gene whose physiological role in the function of the circadian clock has been unclear. Acute Dec1 induction was a prerequisite for ALK-mediated resetting and upregulation was dependent on SMAD3, which was phosphorylated for activation in response to the resetting stimuli. Intraperitoneal injection of TGF-beta into wild-type or Dec1-deficient mice demonstrated that Dec1 has an essential role in phase-shift of clock gene expression in the kidney and adrenal gland. These results indicate that ALK-SMAD3-Dec1 signalling provides an input pathway in the mammalian molecular clock.
生物钟通过外部时间线索进行重置,以与环境变化同步。在哺乳动物中,由Per基因诱导介导的光输入信号通路已得到广泛研究。另一方面,对于独立于Per诱导的重置机制知之甚少。在这里,我们表明,由TGF-β、激活素或碱性信号触发的激活素受体样激酶(ALK)的激活,可独立于Per诱导引起细胞生物钟的重置。这种重置是由Dec1的即时早期诱导介导的,Dec1是一种在生物钟功能中的生理作用尚不清楚的基因。急性Dec1诱导是ALK介导的重置的先决条件,其上调依赖于SMAD3,SMAD3在响应重置刺激时被磷酸化激活。向野生型或Dec1缺陷型小鼠腹腔注射TGF-β表明,Dec1在肾脏和肾上腺中时钟基因表达的相移中起重要作用。这些结果表明,ALK-SMAD3-Dec1信号通路在哺乳动物分子生物钟中提供了一条输入途径。