生物
蛋白质组
昼夜节律
转录组
视交叉上核
生物钟
蛋白质组学
计算生物学
细胞生物学
遗传学
基因
核蛋白
基因表达
图谱
细菌昼夜节律
人类蛋白质组计划
基因表达谱
基因组
蛋白质表达
地图集(解剖学)
突变体
RNA序列
作者
Yuta Otobe,Norie Deki-Arima,Shao Haiying Zheng Xinyan,Kazuma Itabashi,Nobuhiro Kurabayashi,Utaro Nakamura,Anna Uchida,Ryutaro Shimazaki,Kaneyoshi Yamamoto,Takeshi Sakurai,Ying-Hui Fu,Louis J. Ptáček,A. Hirano,Masao Doi,Hikari Yoshitane
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2026-01-01
卷期号:86 (2): 393-406.e3
标识
DOI:10.1016/j.molcel.2025.12.020
摘要
The circadian clock drives daily rhythms of gene expression and physiology. Advances in next-generation DNA sequencing have provided extensive insights into RNA expression, but more functional information at the protein level with sufficient depth has been limited by technical challenges. In this study, we generated a comprehensive mouse circadian proteome atlas (https://chronoproteinology.org/circadian_atlas) by analyzing 32 tissues, including the suprachiasmatic nucleus (SCN), using the next-generation mass spectrometer Orbitrap Astral. Data-independent acquisition of 584 samples, including developmental samples, revealed the spatiotemporal profiles of about 19,000 proteins. Proteome and phospho-proteome analyses of whole-cell and nuclear proteins in the liver revealed circadian changes in protein quantity and quality, as well as global changes in hPER2-S662G mutant mice, a genetic model of human familial advanced sleep phase (FASP). This multi-tissue circadian proteome atlas provides a fundamental resource for understanding when, where, and which proteins are expressed and function.
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