Identification and Analysis of Circadian Clock-Controlled Genes

描述（由申请人提供）：我们的长期目标是用遗传学和生物化学的语言描述构成细胞内昼夜节律系统的反馈循环和途径-它们如何工作，它们如何与环境同步，以及它们产生的时间信息如何用于调节细胞的行为。该建议侧重于模型系统脉孢菌，以及小鼠和哺乳动物细胞系，以了解细胞生理和代谢的昼夜节律控制的基本模式。我们还继续长期的努力，旨在了解脉孢菌的昼夜光感受和光生物学，并利用这一点在一个突出的真菌病原体上开辟新的天地。 在具体目标1中，我们将使用RNA测序、染色质免疫沉淀和生物信息学对脉孢菌的昼夜输出网络进行全面分析和描述，以描述细胞中调控转录的昼夜调节的调控层次。然后，利用脉孢菌独特的生化遗传学背景，我们将跟踪由时钟控制基因编码的蛋白质进行的代谢活动，随着时钟控制活动的出现，我们将开始在脉孢菌代谢图谱上绘制时钟控制过程的光谱，以了解时钟如何调节代谢和生理。 在具体目标2中，我们将利用最近的光感受域的原子水平结构分析，以确定光循环动力学的生物学意义。我们将把光生物学的分析扩展到重要的真菌病原体烟曲霉，在那里我们可以设想一种方法，利用我们对真菌光生物学的理解，为数十万曲霉病患者提供新的治疗方法。 在特定目标3中，我们将使用RNA测序来确定wt和RIP 140敲除细胞的脂肪细胞中时钟控制基因的昼夜节律谱，并将使用脂肪细胞中RIP 140的染色质免疫沉淀来开始剖析这种共激活因子/共抑制因子在这种重要细胞类型的昼夜节律生物学中的作用。我们将寻找RIP 140与已知的生物钟蛋白和与昼夜节律输出有关的转录因子的物理联系，并将产生白色脂肪组织特异性敲除生物钟，以探测小鼠中昼夜节律调节对脂肪代谢的意义，希望能够深入了解糖尿病和代谢综合征。这些项目是互补和相互丰富的，因为它们都依赖于遗传和分子技术来解剖，并最终了解细胞对其环境的反应和真核细胞的组织作为时间的函数。

DESCRIPTION (provided by applicant): Our long term goal is to describe in the language of genetics and biochemistry the feedback cycles and pathways that comprise intracellular circadian systems - how they work, how they are synchronized with the environment, and how time information generated by them is used to regulate the behavior of cells. This proposal focuses on the model system Neurospora, as well as on the mouse and mammalian cell lines, to understand the paradigms underlying circadian control of cell physiology and metabolism. We also continue a longstanding effort aimed at understanding circadian photoreception and photobiology in Neurospora and use this to break new ground on a salient fungal pathogen. In Specific Aim 1, we will carry out a global analysis and description of the circadian output network in Neurospora, using RNA sequencing, chromatin immunoprecipitation, and bioinformatics to describe the regulatory hierarchy governing circadian regulation of transcription in a cell. Then, using the exceptional background of biochemical genetics available in Neurospora, we will track the metabolic activities carried out by the proteins encoded by clock-controlled genes, and as foci of clock-controlled activities emerge, we will begin to lay the spectrum of clock-controlled processes on the Neurospora metabolic map to see how the clock regulates metabolism and physiology. In Specific Aim 2, we will exploit recent atomic level structure analysis of the photoreceptive domain to determine the biological significance of photocycle kinetics. We will extend analysis of photobiology to the important fungal pathogen Aspergillus fumigatus where we can envision a way to exploit our understanding of fungal photobiology to enable a new treatment for hundreds of thousands of patients with aspergillosis. In Specific Aim 3, we will use RNA sequencing to determine the circadian profile of clock-controlled genes in adipocytes of wt and RIP140 knockout cells, and will use chromatin immunoprecipitation of RIP140 in adipocytes to begin to dissect the role of this co-activator/co-repressor in the circadian biology of this important cell type. We will look for physical association of RIP140 with known clock proteins and transcription factors involved with circadian output, and will generate white adipose tissue-specific knockouts of the clock to probe the significance of circadian regulation to fat metabolism in the mouse, hoping to gain insights into diabetes and metabolic syndrome. These projects are complementary and mutually enriching in that they each rely on genetic and molecular techniques to dissect, and ultimately to understand, the response of cells to their environment and the organization of eukaryotic cells as a function of time.