Evolution of the repression mechanisms in circadian clocks

被引:5
作者
Tyler, Jonathan [1 ,2 ]
Lu, Yining [1 ]
Dunlap, Jay [3 ]
Forger, Daniel B. [1 ,4 ]
机构
[1] Univ Michigan, Dept Math, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Pediat, Div Pediat Hematol Oncol, Ann Arbor, MI 48109 USA
[3] Geisel Sch Med Dartmouth, Dept Mol & Syst Biol, Hanover, NH 03755 USA
[4] Univ Michigan, Dept Computat Med & Bioinformat, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
Circadian clocks; Evolution; Transcription; Protein sequestration; Phosphorylation; KAIC PHOSPHORYLATION; FEEDBACK-CONTROL; DYNAMICS; REVEALS; COMPLEX; SYSTEM; WC-1; GENE; TIME; FRQ;
D O I
10.1186/s13059-021-02571-0
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background Circadian (daily) timekeeping is essential to the survival of many organisms. An integral part of all circadian timekeeping systems is negative feedback between an activator and repressor. However, the role of this feedback varies widely between lower and higher organisms. Results Here, we study repression mechanisms in the cyanobacterial and eukaryotic clocks through mathematical modeling and systems analysis. We find a common mathematical model that describes the mechanism by which organisms generate rhythms; however, transcription's role in this has diverged. In cyanobacteria, protein sequestration and phosphorylation generate and regulate rhythms while transcription regulation keeps proteins in proper stoichiometric balance. Based on recent experimental work, we propose a repressor phospholock mechanism that models the negative feedback through transcription in clocks of higher organisms. Interestingly, this model, when coupled with activator phosphorylation, allows for oscillations over a wide range of protein stoichiometries, thereby reconciling the negative feedback mechanism in Neurospora with that in mammals and cyanobacteria. Conclusions Taken together, these results paint a picture of how circadian timekeeping may have evolved.
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页数:18
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