Role of Ror proteins in the mammalian circadian clock

Ror 蛋白在哺乳动物生物钟中的作用

• 批准号: 8328724
• 负责人: STEVE A KAY
• 金额: $ 15.69万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-04-01 至 2012-12-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8328724
• 关键词: Adenoviruses; Architecture; Behavior; Biochemical Pathway; Biological; Biological Clocks; Biological Process; Cell Line; Cell physiology; Cells; ChIP-seq; Circadian Rhythms; Collection; Cues; DNA Binding; Data; Data Set; Diagnostic; Elderly; Environment; Exhibits; Extracellular Protein; Gene Expression; Gene Expression Profile; Genes; Genome; Hepatic; Hepatocyte; Hour; Individual; Length; Libraries; Ligands; Liver; Mass Spectrum Analysis; Mediating; Metabolic; Metabolic Pathway; Metabolic syndrome; Metabolism; Methods; Modeling; Molecular Profiling; Mus; Nature; Nuclear Hormone Receptors; Organism; Output; Pacemakers; Pathway interactions; Peripheral; Physiological; Physiological Processes; Physiology; Process; Property; Proteins; Proteome; Regulation; Role; Screening procedure; Signal Pathway; Signal Transduction; Slave; System; Techniques; Therapeutic; Time; Tissues; Transcript; Validation; base; cell growth regulation; cell type; chromatin immunoprecipitation; circadian pacemaker; extracellular; genetic manipulation; high throughput screening; human disease; immortalized cell; improved; in vivo; insight; knowledge base; lipid metabolism; meetings; metabolic abnormality assessment; metabolomics; mouse model; network models; novel; receptor; suprachiasmatic nucleus; transcription factor; transcriptomics; vector

DESCRIPTION (provided by applicant): Circadian rhythms exist in almost all organisms to anticipate the daily changes in the environment and to temporally coordinate biological processes. Although much progress has been made to identify the components of the mammalian clock and the mechanisms by which it controls physiology, the knowledge base is by no means complete. We propose to further elucidate the architecture of the liver clock and its relationship with metabolism by generating and integrating divergent types of large-scale data, followed by validation of these data in vivo. In order to isolate and study the cell-autonomous clock, we have identified a unique cell line, Met Murine Hepatocyte-Day 3 (MMH-D3) that retains many metabolic functions and exhibits robust circadian rhythms. Thus we will be able to interrogate both the clock and metabolic pathways and study their interactions. We have already obtained transcriptomic and metabolomic data for MMH-D3 time-courses (every 2-hours for 48-hours) to identify cycling entities. Furthermore, we will perform chromatin immunoprecipitation followed by sequencing (ChIP-seq) for REV-ERB1, a nuclear hormone receptor that is part of the clock and a regulator of lipid metabolism, to explore one of the mechanisms of how the clock controls metabolism. To identify novel proteins that act as systemic cues for the liver clock, we will perform high- throughput screening of an invaluable library of over 6,000 secreted proteins. To our knowledge, this is one of the broadest and diverse data sets collected for the analysis of the circadian clock. To generate the most comprehensive model of the clock, these data sets will not only be evaluated individually, but will be integrated to reconstruct biological networks using methods based on vector auto-regression. Such networks have the ability to predict regulation and interaction within and between the different layers, as well as their associations with metabolic pathways. The hypotheses generated by the network model will be verified using adenovirus techniques in vivo, which will also enable us to differentiate between cell-autonomous and systemic signals governing the liver clock. The clock clearly has an influence on proper physiological function, thus a better understanding of circadian clockwork will improve our understanding of the mechanisms that underlie human disease; this will refine diagnostic and therapeutic strategies.

描述（由申请人提供）：几乎所有生物体都存在昼夜节律，以预测环境的日常变化并暂时协调生物过程。尽管在确定哺乳动物生物钟的组成部分及其控制生理机能的机制方面已经取得了很大进展，但知识库绝不完整。我们建议通过生成和整合不同类型的大规模数据，然后在体内验证这些数据，进一步阐明肝脏时钟的结构及其与新陈代谢的关系。为了分离和研究细胞自主时钟，我们鉴定了一种独特的细胞系，Met Murine Hepat cell-Day 3 (MMH-D3)，它保留了许多代谢功能并表现出强大的昼夜节律。因此，我们将能够询问时钟和代谢途径并研究它们的相互作用。我们已经获得了 MMH-D3 时间进程（48 小时内每 2 小时一次）的转录组学和代谢组学数据，以识别循环实体。此外，我们将对REV-ERB1进行染色质免疫沉淀和测序（ChIP-seq），REV-ERB1是一种核激素受体，是生物钟的一部分，也是脂质代谢的调节因子，以探索生物钟控制代谢的机制之一。为了识别充当肝脏时钟系统线索的新型蛋白质，我们将对包含 6,000 多种分泌蛋白质的宝贵库进行高通量筛选。据我们所知，这是为分析生物钟而收集的最广泛和多样化的数据集之一。为了生成最全面的时钟模型，这些数据集不仅将被单独评估，还将使用基于向量自回归的方法进行集成以重建生物网络。这种网络能够预测不同层内部和之间的调节和相互作用，以及它们与代谢途径的关联。网络模型产生的假设将在体内使用腺病毒技术进行验证，这也将使我们能够区分控制肝脏时钟的细胞自主信号和系统信号。生物钟显然对正常的生理功能有影响，因此更好地了解昼夜节律将提高我们对人类疾病机制的理解；这将完善诊断和治疗策略。