Network Features of the Mammalian Circadian Clock

被引:202
作者
Baggs, Julie E. [1 ,2 ]
Price, Tom S. [1 ,2 ,3 ]
DiTacchio, Luciano [4 ]
Panda, Satchidananda [4 ]
FitzGerald, Garret A. [1 ,2 ]
Hogenesch, John B. [1 ,2 ]
机构
[1] Univ Penn, Sch Med, Dept Pharmacol, Philadelphia, PA 19104 USA
[2] Univ Penn, Sch Med, Inst Translat Med & Therapeut, Philadelphia, PA 19104 USA
[3] Kings Coll London, MRC, SGDP Ctr, Inst Psychiat, London WC2R 2LS, England
[4] Salk Inst Biol Studies, La Jolla, CA 92037 USA
来源
PLOS BIOLOGY | 2009年 / 7卷 / 03期
基金
美国国家卫生研究院;
关键词
REV-ERB; CRYPTOCHROME PROTEINS; BACKUP CIRCUITS; GENE; TRANSCRIPTION; REVEALS; PERIOD; OSCILLATORS; FIBROBLASTS; ROBUSTNESS;
D O I
10.1371/journal.pbio.1000052
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian circadian clock is a cell-autonomous system that drives oscillations in behavior and physiology in anticipation of daily environmental change. To assess the robustness of a human molecular clock, we systematically depleted known clock components and observed that circadian oscillations are maintained over a wide range of disruptions. We developed a novel strategy termed Gene Dosage Network Analysis (GDNA) in which small interfering RNA (siRNA)-induced dose-dependent changes in gene expression were used to build gene association networks consistent with known biochemical constraints. The use of multiple doses powered the analysis to uncover several novel network features of the circadian clock, including proportional responses and signal propagation through interacting genetic modules. We also observed several examples where a gene is up-regulated following knockdown of its paralog, suggesting the clock network utilizes active compensatory mechanisms rather than simple redundancy to confer robustness and maintain function. We propose that these network features act in concert as a genetic buffering system to maintain clock function in the face of genetic and environmental perturbation.
引用
收藏
页码:563 / 575
页数:13
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