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Chromatin Remodeling and Circadian Clock Control

染色质重塑和昼夜节律时钟控制

基本信息

批准号：
8315052
负责人：
Paolo Sassone-Corsi
金额：
$ 8.7万
依托单位：
UNIVERSITY OF CALIFORNIA-IRVINE
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-08-01 至 2012-07-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8315052
关键词：
Acetylation Biochemical Biological Cell physiology Cells Chromatin Chromatin Remodeling Factor Circadian Rhythms Complex Constitution Coronary heart disease DNA Dissection Elements Goals Health Histone H3 Histones Hormonal Human In Vitro Jet Lag Syndrome Link Mediating Mental Depression Metabolic Metabolism Modification Molecular Molecular Genetics NCOA3 gene Nature Neurodegenerative Disorders Organism PCAF gene Physiological Physiology Positioning Attribute Post-Translational Protein Processing Process Proteins Regulation Role Second Messenger Systems Signal Pathway Signal Transduction Sleep Wake Cycle Sleeplessness Specificity Stimulus System Therapeutic Time Transcript Transcriptional Regulation Translating base chromatin remodeling circadian pacemaker environmental change genome-wide histone acetyltransferase in vivo insight novel response scaffold second messenger tool development

项目摘要

DESCRIPTION (provided by applicant): A remarkable variety of fundamental physiological functions in most organisms is controlled by the circadian clock. This is a time-tracking system intrinsic to most organisms that enables the adaptation to environmental changes. Disruption of circadian rhythms has profound influence to human health and has been linked to depression, insomnia, jet lag, coronary heart disease and a variety of neurodegenerative diseases. Thereby, the molecular mechanisms governing the circadian clock constitute a very attractive hold for the understanding of the links to physiology and metabolism, representing potential tools for the development of therapeutic strategies. Remarkably, 10-15% of all mammalian transcripts undergo circadian fluctuations in their expression levels. Thus, genome-wide mechanisms must operate in order to insure such global transcriptional regulation. Our recent studies (Cell 2006 125: 497-508) have established that CLOCK, a master controller of circadian rhythms, directly modifies chromatin. CLOCK possesses intrinsic enzymatic histone acetyltransferase (HAT) activity, demonstrating that control of chromatin remodeling constitutes a key regulatory step governing the circadian clock machinery. This finding has multiple molecular and physiological implications and paves the way to a number of important in vitro and in vivo studies that are central to this proposal. We will use a range of molecular, genetic and biochemical approaches to gain insights into chromatin remodeling mechanisms that are likely to govern the physiological mechanism of the circadian clock. Another goal is to unravel how clock-mediated signaling may 'talk' to the enzymatic function of CLOCK, and thereby establish a direct link between physiology and chromatin remodeling. A final goal is to decipher the extent of CLOCK-mediated acetylation, by identifying the natural substrates of its enzymatic activity. We predict that these studies will provide novel and important insights into how circadian physiology and metabolism are controlled by chromatin remodeling. The circadian clock governs a large variety of our rhythmic physiology, including sleep-wake cycles, metabolism and hormonal levels. This proposal is aimed at deciphering the intimate mechanisms by which the circadian clock operates. Specifically, we will unravel the function that chromatin, the proteinaceous scaffold of DNA, has in these processes.

描述（由申请人提供）：在大多数生物体中，生物钟控制着多种显著的基本生理功能。这是大多数生物体固有的时间跟踪系统，使其能够适应环境变化。昼夜节律的紊乱对人类健康有着深远的影响，并与抑郁症、失眠、时差、冠心病和各种神经退行性疾病有关。因此，控制生物钟的分子机制构成了一个非常有吸引力的持有的生理学和代谢的联系的理解，代表潜在的工具，为发展的治疗策略。值得注意的是，所有哺乳动物转录物的10-15%经历其表达水平的昼夜节律波动。因此，全基因组机制必须运作，以确保这种全球转录调控。我们最近的研究（Cell 2006 125：497-508）已经确定，昼夜节律的主控制器CLOCK直接修饰染色质。CLOCK具有内在的酶促组蛋白乙酰转移酶（HAT）活性，表明染色质重塑的控制构成了控制生物钟机制的关键调节步骤。这一发现具有多种分子和生理学意义，并为许多重要的体外和体内研究铺平了道路，这些研究对这一提议至关重要。我们将使用一系列的分子，遗传和生物化学方法来深入了解染色质重塑机制，这些机制可能会控制昼夜节律钟的生理机制。另一个目标是揭示时钟介导的信号如何与CLOCK的酶功能“对话”，从而建立生理学和染色质重塑之间的直接联系。最终目标是通过鉴定其酶活性的天然底物来破译CLOCK介导的乙酰化的程度。我们预测，这些研究将提供新的和重要的见解昼夜生理和代谢是如何控制染色质重塑。生物钟控制着我们各种各样的节奏生理，包括睡眠-觉醒周期，新陈代谢和激素水平。这项提议旨在破译生物钟运作的内在机制。具体来说，我们将揭开染色质，DNA的蛋白质支架，在这些过程中的功能。