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The CRTC1-SIK1 pathway regulates entrainment of the circadian clock

机译:CRTC1-SIK1通路调节生物钟的携带

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Retinal photoreceptors entrain the circadian system to the solar day. This photic resetting involves cAMP response element binding protein (CREB)-mediated upregulation of Per genes within individual cells of the suprachiasmatic nuclei (SCN). Our detailed understanding of this pathway is poor, and it remains unclear why entrainment to a new time zone takes several days. By analyzing the light-regulated transcriptome of the SCN, we have identified a key role for salt inducible kinase 1 (SIK1) and CREB-regulated transcription coactivator 1 (CRTC1) in clock re-setting. An entrainment stimulus causes CRTC1 to coactivate CREB, inducing the expression of Per1 and Sik1. SIK1 then inhibits further shifts of the clock by phosphorylation and deactivation of CRTC1. Knockdown of Sik1 within the SCN results in increased behavioral phase shifts and rapid re-entrainment following experimental jet lag. Thus SIK1 provides negative feedback, acting to suppress the effects of light on the clock. This pathway provides a potential target for the regulation of circadian rhythms.
机译:视网膜感光器将昼夜节律系统带到太阳日。这种光复性复位涉及cAMP反应元件结合蛋白(CREB)介导的视交叉上核(SCN)单个细胞内Per基因的上调。我们对该途径的详细了解很差,并且尚不清楚为什么将一个新的时区带入需要几天的时间。通过分析SCN的光调节转录组,我们确定了盐诱导激酶1(SIK1)和CREB调节转录共激活因子1(CRTC1)在时钟重置中的关键作用。夹带刺激使CRTC1共同激活CREB,从而诱导Per1和Sik1的表达。然后,SIK1通过CRTC1的磷酸化和去激活来抑制时钟的进一步偏移。在SCN中抑制Sik1会导致行为相移增加,并在实验时差后迅速重新夹带。因此,SIK1提供负反馈,以抑制光对时钟的影响。该途径为调节昼夜节律提供了潜在的靶标。

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