Department of Biological Sciences, Vanderbilt University, Nashville, TN 37235, USA.
Annu Rev Biophys. 2011;40:143-67. doi: 10.1146/annurev-biophys-042910-155317.
Recent studies have unveiled the molecular machinery responsible for the biological clock in cyanobacteria and found that it exerts pervasive control over cellular processes including global gene expression. Indeed, the entire chromosome undergoes daily cycles of topology/compaction! The circadian system comprises both a posttranslational oscillator (PTO) and a transcriptional/translational feedback loop (TTFL). The PTO can be reconstituted in vitro with three purified proteins (KaiA, KaiB, and KaiC) and ATP. These are the only circadian proteins for which high-resolution structures are available. Phase in this nanoclockwork has been associated with key phosphorylations of KaiC. Structural considerations illuminate the mechanism by which the KaiABC oscillator ratchets unidirectionally. Models of the complete in vivo system have important implications for our understanding of circadian clocks in higher organisms, including mammals. The conjunction of structural, biophysical, and biochemical approaches to this system has brought our understanding of the molecular mechanisms of biological timekeeping to an unprecedented level.
最近的研究揭示了蓝藻生物钟的分子机制,并发现它对包括全局基因表达在内的细胞过程施加了普遍的控制。事实上,整个染色体经历着拓扑/压缩的每日循环!生物钟系统包括一个翻译后振荡器(PTO)和一个转录/翻译反馈环(TTFL)。PTO 可以用三种纯化的蛋白质(KaiA、KaiB 和 KaiC)和 ATP 在体外重建。这些是唯一具有高分辨率结构的生物钟蛋白。这个纳米钟的相位与 KaiC 的关键磷酸化有关。结构考虑阐明了 KaiABC 振荡器单向棘轮的机制。完整的体内系统模型对我们理解包括哺乳动物在内的高等生物的生物钟具有重要意义。对该系统的结构、生物物理和生化方法的结合使我们对生物钟的分子机制的理解达到了前所未有的水平。