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