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Genome Res. 2021 Feb;31(2):171-185. doi: 10.1101/gr.263814.120. Epub 2021 Jan 12.
2
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Cell Commun Signal. 2020 Nov 11;18(1):181. doi: 10.1186/s12964-020-00658-y.
3
Proteomic analysis of Drosophila CLOCK complexes identifies rhythmic interactions with SAGA and Tip60 complex component NIPPED-A.果蝇 CLOCK 复合物的蛋白质组分析鉴定了与 SAGA 和 Tip60 复合物成分 NIPPED-A 的节律性相互作用。
Sci Rep. 2020 Oct 21;10(1):17951. doi: 10.1038/s41598-020-75009-5.
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BMAL1 Associates with NOP58 in the Nucleolus and Contributes to Pre-rRNA Processing.BMAL1与核仁中的NOP58相关联并有助于前体rRNA加工。
iScience. 2020 Jun 26;23(6):101151. doi: 10.1016/j.isci.2020.101151. Epub 2020 May 12.
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Molecular mechanisms and physiological importance of circadian rhythms.昼夜节律的分子机制和生理重要性。
Nat Rev Mol Cell Biol. 2020 Feb;21(2):67-84. doi: 10.1038/s41580-019-0179-2. Epub 2019 Nov 25.
6
Splice variants of DOMINO control Drosophila circadian behavior and pacemaker neuron maintenance.DOMINO 剪接变异体控制果蝇的生物钟行为和起搏神经元的维持。
PLoS Genet. 2019 Oct 28;15(10):e1008474. doi: 10.1371/journal.pgen.1008474. eCollection 2019 Oct.
7
Nipped-A regulates the Drosophila circadian clock via histone deubiquitination.Nipped-A 通过组蛋白去泛素化调节果蝇的生物钟。
EMBO J. 2020 Jan 2;39(1):e101259. doi: 10.15252/embj.2018101259. Epub 2019 Sep 19.
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Intense Light-Mediated Circadian Cardioprotection via Transcriptional Reprogramming of the Endothelium.强光介导的通过内皮细胞转录重编程的昼夜节律心脏保护。
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9
The Phospho-Code Determining Circadian Feedback Loop Closure and Output in Neurospora.磷酸化密码决定Neurospora 中昼夜反馈回路的闭合和输出。
Mol Cell. 2019 May 16;74(4):771-784.e3. doi: 10.1016/j.molcel.2019.03.003. Epub 2019 Apr 3.
10
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Eur J Neurosci. 2020 Jan;51(1):182-193. doi: 10.1111/ejn.14318. Epub 2019 Jan 30.

昼夜节律蛋白质组学:核心时钟以外的蛋白质-蛋白质相互作用研究如何影响昼夜节律计时模型。

Circadian Interactomics: How Research Into Protein-Protein Interactions Beyond the Core Clock Has Influenced the Model of Circadian Timekeeping.

机构信息

Department of Biological Sciences, Rensselaer Polytechnic Institute, Troy, NY.

Center for Biotechnology & Interdisciplinary Sciences, Rensselaer Polytechnic Institute, Troy, NY.

出版信息

J Biol Rhythms. 2021 Aug;36(4):315-328. doi: 10.1177/07487304211014622. Epub 2021 May 31.

DOI:10.1177/07487304211014622
PMID:34056936
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8830082/
Abstract

The circadian clock is the broadly conserved, protein-based, timekeeping mechanism that synchronizes biology to the Earth's 24-h light-dark cycle. Studies of the mechanisms of circadian timekeeping have placed great focus on the role that individual protein-protein interactions play in the creation of the timekeeping loop. However, research has shown that clock proteins most commonly act as part of large macromolecular protein complexes to facilitate circadian control over physiology. The formation of these complexes has led to the large-scale study of the proteins that comprise these complexes, termed here "circadian interactomics." Circadian interactomic studies of the macromolecular protein complexes that comprise the circadian clock have uncovered many basic principles of circadian timekeeping as well as mechanisms of circadian control over cellular physiology. In this review, we examine the wealth of knowledge accumulated using circadian interactomics approaches to investigate the macromolecular complexes of the core circadian clock, including insights into the core mechanisms that impart circadian timing and the clock's regulation of many physiological processes. We examine data acquired from the investigation of the macromolecular complexes centered on both the activating and repressing arm of the circadian clock and from many circadian model organisms.

摘要

生物钟是一种广泛保守的、基于蛋白质的计时机制,它使生物与地球的 24 小时光-暗循环同步。对生物钟机制的研究非常关注个体蛋白-蛋白相互作用在计时环形成中的作用。然而,研究表明,时钟蛋白通常作为大型大分子蛋白复合物的一部分发挥作用,以促进生物钟对生理的控制。这些复合物的形成导致了对构成这些复合物的蛋白质的大规模研究,这里称为“生物钟相互作用组学”。对构成生物钟的大分子蛋白复合物的生物钟相互作用组学研究揭示了许多生物钟计时的基本原理以及生物钟对细胞生理的控制机制。在这篇综述中,我们检查了使用生物钟相互作用组学方法研究核心生物钟的大分子复合物所积累的丰富知识,包括赋予生物钟计时的核心机制以及生物钟对许多生理过程的调节的见解。我们检查了从对以生物钟的激活和抑制臂为中心的大分子复合物的研究以及从许多生物钟模式生物中获得的数据。