Molecular Mechanisms Integrating Circadian Timing and Photic Signaling

整合昼夜节律和光信号传导的分子机制

基本信息

批准号：
10112971
负责人：
Ravi Allada
金额：
$ 34.56万
依托单位：
NORTHWESTERN UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2018
资助国家：
美国
起止时间：
2018-05-01 至 2023-02-28
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/10112971
关键词：
Address Affect Alleles Animals Automobile Driving Behavior Behavioral Biological Process Cell Line Cells Communication Coupling Data Dependence Disease Drosophila genus Environment Feedback Gap Junctions Genetic Genetic Transcription Hour Impairment Jet Lag Syndrome Length Light Literature Mediating Modeling Molecular Molecular Genetics Motor Activity Neurons Pacemakers Pathway interactions Periodicity Phase Phenotype Phosphorylation Phosphotransferases Photoperiod Photoreceptors Physiologic pulse Protein Dephosphorylation Publishing Regulation Research Role Signal Pathway Signal Transduction Site Sleeplessness Speed System Testing Time Visual Work cell type circadian circadian pacemaker day length gene function genetic analysis genetic manipulation genetic resource insight intercellular communication light effects molecular clock mutant neural network architecture nonvisual photoreceptor novel phosphatase of regenerating liver relating to nervous system response shift work

Address Affect Alleles Animals Automobile Driving Behavior Behavioral Biological Process Cell Line Cells Communication Coupling Data Dependence Disease Drosophila genus Environment Feedback Gap Junctions Genetic Genetic Transcription Hour Impairment Jet Lag Syndrome Length Light Literature Mediating Modeling Molecular Molecular Genetics Motor Activity Neurons Pacemakers Pathway interactions Periodicity Phase Phenotype Phosphorylation Phosphotransferases Photoperiod Photoreceptors Physiologic pulse Protein Dephosphorylation Publishing Regulation Research Role Signal Pathway Signal Transduction Site Sleeplessness Speed System Testing Time Visual Work cell type circadian circadian pacemaker day length gene function genetic analysis genetic manipulation genetic resource insight intercellular communication light effects molecular clock mutant neural network architecture nonvisual photoreceptor novel phosphatase of regenerating liver relating to nervous system response shift work

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项目摘要

Project Summary Circadian clocks have evolved to appropriately align biological processes to the changing 24 h environment. Genetic analyses of circadian locomotor activity rhythms in the fruit fly Drosophila have revealed transcriptional feedback loops as the core organizing principle of circadian clocks. Yet the pace of these circadian feedback loops is largely determined by protein phosphorylation and subsequent degradation, driving rhythmic expression of clock components such as PERIOD (PER). In Drosophila, light is able to reset these oscillators in part via degradation of the clock component TIMELESS (TIM). Remarkably, these clocks are highly conserved among animals. Circadian clocks also enable the appropriate adaptation to seasonal changes in day length or photoperiod. Yet while much is known about both core clock and photic input mechanisms, a mechanistic understanding of how these two pathways collaborate to mediate responses light, including changing photoperiod, is lacking in animals. Here a novel clock component has been discovered, the phosphatase of regenerating liver-1 (PRL-1), that is also important for light mediated resetting and setting behavioral phase under varying seasonal photoperiod. This research proposes to leverage the discovery of PRL-1 to understand how the circadian clock integrates light information to drive appropriately timed behavior. It will specifically address the neuronal basis of PRL-1 function including the role in specific photoreceptor pathways, its function in autonomous and coupling neuronal oscillators, and the role of the light and clock regulated clock component TIM in mediating PRL-1 effects. These studies exploit the discovery of a core clock component with a novel role in photoperiod-dependent behavior. In addition, full advantage is taken of the Drosophila system, including the conservation of the core clock machinery and clock neural network architecture as well as extensive molecular genetic resources to examine gene function in the whole animal. This research also leverages the ability to quantitatively examine molecular oscillations in FACS sorted and intact neurons. This work could provide insights into how circadian clocks integrate environmental information to yield timed behavior.

项目摘要昼夜节律钟已经演变为适当地使生物学过程与24小时的环境变化。果蝇果蝇中昼夜节律活性节奏的遗传分析显示了转录反馈循环是昼夜节律的核心组织原理。然而这些昼夜节律的节奏循环在很大程度上取决于蛋白质磷酸化和随后的降解，驱动有节奏的时钟组件（例如周期）的表达（per）。在果蝇中，光能够重置这些振荡器部分通过时钟组件永恒的降解（TIM）。值得注意的是，这些时钟很高在动物中保守。昼夜节律时钟还可以适当适应季节性变化白天长度或光周期。然而，尽管对核心时钟和光学输入机制众所周知，但机械理解这两种途径如何合作调解反应的光线，包括变化的光周期，动物缺乏。在这里发现了一个新颖的时钟组件，再生肝脏1（PRL-1）的磷酸酶，这对于光介导的重置和设置也很重要在不同的季节光周期下的行为阶段。这项研究提议利用发现 PRL-1了解昼夜节律如何整合光信息以推动适当的定时行为。它将特别解决PRL-1功能的神经元基础，包括在特定光感受器中的作用途径，其在自主和耦合神经元振荡器中的功能以及光和时钟的作用调节的时钟成分TIM介导PRL-1效应。这些研究利用了核心时钟的发现在光周期依赖性行为中具有新作用的成分。此外，对果蝇系统，包括核心时钟机械和时钟神经网络的保护建筑以及广泛的分子遗传资源，以检查整个动物的基因功能。这项研究还利用了定量检查FACS分类和分子振荡的能力完整的神经元。这项工作可以提供有关昼夜节律如何整合环境信息的见解产生定时行为。