Biochemistry Center, Heidelberg University, Im Neuenheimer Feld 328, Heidelberg D-69120, Germany.
Biochemistry Center, Heidelberg University, Im Neuenheimer Feld 328, Heidelberg D-69120, Germany.
J Mol Biol. 2020 May 29;432(12):3449-3465. doi: 10.1016/j.jmb.2020.04.004. Epub 2020 Apr 17.
Circadian clocks are self-sustained oscillators that orchestrate metabolism and physiology in synchrony with the 24-h day-night cycle. They are temperature compensated over a wide range and entrained by daily recurring environmental cues. Eukaryotic circadian clocks are governed by cell-based transcriptional-translational feedback loops (TTFLs). The core components of the TTFLs are largely known and their molecular interactions in many cases well established. Although the core clock components are not or only partly conserved, the molecular wiring of TTFLs is rather similar across kingdoms and phylae. In all known systems, circadian timing relies critically on casein kinase 1 (CK1) and CK1-dependent hyperphosphorylation of core clock proteins, in particular of negative elements of the TTFLs. Yet, we lack concepts as to how phosphorylation by CK1a and other kinases relates to timekeeping on the molecular level. Here we summarize what is known about phosphorylation of core components of the circadian clock of Neurospora crassa and speculate about the molecular basis of circadian timekeeping by hyperphosphorylation of intrinsically disordered regions in clock proteins.
生物钟是自我维持的振荡器,与 24 小时/天-夜周期同步协调代谢和生理学。它们在很大的温度范围内得到补偿,并通过每天重复出现的环境线索进行同步调整。真核生物钟由基于细胞的转录-翻译反馈环(TTFL)控制。TTFL 的核心组件在很大程度上是已知的,它们在许多情况下的分子相互作用也已经确立。尽管核心时钟组件没有或只有部分保守,但 TTFL 的分子布线在不同的王国和类群中非常相似。在所有已知的系统中,生物钟计时都严重依赖于酪蛋白激酶 1(CK1)和 CK1 依赖性的核心时钟蛋白的过度磷酸化,特别是 TTFL 的负元件。然而,我们缺乏关于 CK1a 和其他激酶的磷酸化如何与分子水平上的计时相关的概念。在这里,我们总结了粗糙脉孢菌生物钟核心成分的磷酸化的已知情况,并推测了通过时钟蛋白中无序区域的过度磷酸化来实现生物钟计时的分子基础。