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A proteomics landscape of circadian clock in mouse liver
被引:109
|作者:
Wang, Yunzhi
[1
]
Song, Lei
[2
]
Liu, Mingwei
[3
]
Ge, Rui
[1
]
Zhou, Quan
[3
]
Liu, Wanlin
[3
]
Li, Ruiyang
[1
]
Qie, Jingbo
[1
]
Zhen, Bei
[3
]
Wang, Yi
[3
]
He, Fuchu
[1
,2
,3
]
Qin, Jun
[1
,3
,4
]
Ding, Chen
[1
]
机构:
[1] Fudan Univ, Zhongshan Hosp, Sch Life Sci, Human Phenome Inst,Inst Biomed Sci,State Key Lab, Shanghai 200032, Peoples R China
[2] Tsinghua Univ, Sch Life Sci, Beijing 100084, Peoples R China
[3] Natl Ctr Prot Sci, Beijing Proteome Res Ctr, State Key Lab Prote, Beijing 102206, Peoples R China
[4] Baylor Coll Med, Dept Mol & Cellular Biol, Verna & Marrs McLean Dept Biochem & Mol Biol, Alkek Ctr Mol Discovery, Houston, TX 77030 USA
来源:
基金:
国家重点研发计划;
对外科技合作项目(国际科技项目);
中国国家自然科学基金;
关键词:
KUPFFER CELLS;
METABOLISM;
PHOSPHORYLATION;
QUANTIFICATION;
TRANSCRIPTION;
EXPRESSION;
PHYSIOLOGY;
MACROPHAGES;
LINKS;
CYCLE;
D O I:
10.1038/s41467-018-03898-2
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
As a circadian organ, liver executes diverse functions in different phase of the circadian clock. This process is believed to be driven by a transcription program. Here, we present a transcription factor (TF) DNA-binding activity-centered multi-dimensional proteomics landscape of the mouse liver, which includes DNA-binding profiles of different TFs, phosphorylation, and ubiquitylation patterns, the nuclear sub-proteome, the whole proteome as well as the transcriptome, to portray the hierarchical circadian clock network of this tissue. The TF DNA-binding activity indicates diurnal oscillation in four major pathways, namely the immune response, glucose metabolism, fatty acid metabolism, and the cell cycle. We also isolate the mouse liver Kupffer cells and measure their proteomes during the circadian cycle to reveal a cell-type resolved circadian clock. These comprehensive data sets provide a rich data resource for the understanding of mouse hepatic physiology around the circadian clock.
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页数:16
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