The Proteomic Landscape of the Suprachiasmatic Nucleus Clock Reveals Large-Scale Coordination of Key Biological Processes

被引:49
作者
Chiang, Cheng-Kang [1 ,2 ]
Mehta, Neel [3 ]
Patel, Abhilasha [3 ]
Zhang, Peng [3 ]
Ning, Zhibin [1 ,2 ]
Mayne, Janice [1 ,2 ]
Sun, Warren Y. L. [1 ,2 ]
Cheng, Hai-Ying M. [3 ]
Figeys, Daniel [1 ,2 ]
机构
[1] Univ Ottawa, Fac Med, Ottawa Inst Syst Biol, Ottawa, ON, Canada
[2] Univ Ottawa, Fac Med, Dept Biochem Microbiol & Immunol, Ottawa, ON, Canada
[3] Univ Toronto Mississauga, Dept Biol, Mississauga, ON, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
CIRCADIAN-CLOCK; MOUSE; TRANSCRIPTION; ACTIVATION; EXPRESSION; MECHANISM; LIGHT; CYCLE;
D O I
10.1371/journal.pgen.1004695
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The suprachiasmatic nucleus (SCN) acts as the central clock to coordinate circadian oscillations in mammalian behavior, physiology and gene expression. Despite our knowledge of the circadian transcriptome of the SCN, how it impacts genomewide protein expression is not well understood. Here, we interrogated the murine SCN proteome across the circadian cycle using SILAC-based quantitative mass spectrometry. Of the 2112 proteins that were accurately quantified, 20% (421 proteins) displayed a time-of-day-dependent expression profile. Within this time-of-day proteome, 11% (48 proteins) were further defined as circadian based on a sinusoidal expression pattern with a similar to 24 h period. Nine circadianly expressed proteins exhibited 24 h rhythms at the transcript level, with an average time lag that exceeded 8 h. A substantial proportion of the time-of-day proteome exhibited abrupt fluctuations at the anticipated light-to-dark and dark-to-light transitions, and was enriched for proteins involved in several key biological pathways, most notably, mitochondrial oxidative phosphorylation. Additionally, predicted targets of miR-133ab were enriched in specific hierarchical clusters and were inversely correlated with miR133ab expression in the SCN. These insights into the proteomic landscape of the SCN will facilitate a more integrative understanding of cellular control within the SCN clock.
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页数:15
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