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磷酸化密码决定Neurospora 中昼夜反馈回路的闭合和输出。

The Phospho-Code Determining Circadian Feedback Loop Closure and Output in Neurospora.

机构信息

Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH 03755, USA.

Norris Cotton Cancer Center, Geisel School of Medicine at Dartmouth, Hanover, NH 03755, USA; Department of Biochemistry and Cell Biology, Geisel School of Medicine at Dartmouth, Hanover, NH 03755, USA.

出版信息

Mol Cell. 2019 May 16;74(4):771-784.e3. doi: 10.1016/j.molcel.2019.03.003. Epub 2019 Apr 3.

Abstract

In the negative feedback loop driving fungal and animal circadian oscillators, negative elements (FREQUENCY [FRQ], PERIODS [PERs], and CRYPTOCHROMES [CRYs]) are understood to inhibit their own expression, in part by promoting the phosphorylation of their heterodimeric transcriptional activators (e.g., White Collar-1 [WC-1]-WC-2 [White Collar complex; WCC] and BMAL1/Circadian Locomotor Output Cycles Kaput [CLOCK]). However, correlations between heterodimer activity and phosphorylation are weak, contradictions exist, and mechanistic details are almost wholly lacking. We report mapping of 80 phosphosites on WC-1 and 15 on WC-2 and elucidation of the time-of-day-specific code, requiring both a group of phosphoevents on WC-1 and two distinct clusters on WC-2, that governs circadian repression, leading to feedback loop closure. Combinatorial control via phosphorylation also governs rhythmic WCC binding to the promoters of clock-controlled genes mediating the essential first step in circadian output, a group encoding both transcription factors and signaling proteins. These data provide a basic mechanistic understanding for fundamental events underlying circadian negative feedback and output, key aspects of circadian biology.

摘要

在驱动真菌和动物生物钟振荡器的负反馈环中,负元件(频率[FRQ]、周期[PERs]和隐色素[CRYs])被理解为抑制自身表达,部分是通过促进其异二聚体转录激活物(例如,White Collar-1[WC-1]-WC-2[White Collar 复合物;WCC]和 BMAL1/Circadian Locomotor Output Cycles Kaput[CLOCK])的磷酸化。然而,异二聚体活性与磷酸化之间的相关性很弱,存在矛盾,而且机制细节几乎完全缺失。我们报告了对 WC-1 上的 80 个磷酸化位点和 WC-2 上的 15 个磷酸化位点进行了作图,并阐明了昼夜特异性密码,该密码需要 WC-1 上的一组磷酸化事件和 WC-2 上的两个不同簇,从而控制生物钟的负反馈,导致反馈环闭合。通过磷酸化进行的组合控制还控制着 WCC 与时钟控制基因启动子的节律性结合,这些基因介导生物钟输出的基本第一步,其中一组编码转录因子和信号蛋白。这些数据为生物钟负反馈和输出的基本事件提供了基本的机制理解,这是生物钟生物学的关键方面。

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