4.5 Review Book Chapter

The Cyanobacterial Circadian System: From Biophysics to Bioevolution

期刊

ANNUAL REVIEW OF BIOPHYSICS, VOL 40
卷 40, 期 -, 页码 143-167

出版社

ANNUAL REVIEWS
DOI: 10.1146/annurev-biophys-042910-155317

关键词

cyanobacteria; Kai; KaiABC; cell division; in vitro oscillators

资金

  1. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM067152, R01GM081646, R01GM073845, R01GM088595] Funding Source: NIH RePORTER
  2. NIGMS NIH HHS [R01 GM081646, GM088595, R01 GM088595-02, R01 GM073845, R01 GM067152-10, R01 GM088595, GM073845, GM067152, R01 GM081646-02, R37 GM067152, GM081646, R01 GM073845-06, R01 GM067152] Funding Source: Medline

向作者/读者索取更多资源

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 M 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.

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