Interdisciplinary studies of the Drosophila Circadian Clock

果蝇昼夜节律钟的跨学科研究

• 批准号: 7176034
• 负责人: Michael Warren Young
• 金额: $ 36.92万
• 依托单位: ROCKEFELLER UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-02-03 至 2010-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7176034
• 关键词: Affect; Amino Acids; Area; Behavior; Behavioral; Binding; Biochemical Genetics; Biological Models; Chloride Anion Exchanger; Circadian Rhythms; Class; Daily; Data; Depth; Development; Drosophila genus; Elements; Fishes; Flavins; Gene Expression; Gene Proteins; Genes; Genome; Glycogen Synthase Kinase 3; Head; Homologous Gene; Human; Individual; Interdisciplinary Study; Investigation; Lethal Genes; Life; Light; Link; Maps; Molecular; Mus; Mutation; Mutation Analysis; Orthologous Gene; Output; Periodicity; Phosphorylation; Physiological; Physiology; Protein Splicing; Proteins; Protocols documentation; Rana; Recovery; Reporting; Research; Role; SLC26A3 gene; Series; Structure; Techniques; Tissues; Vertebrates; Work; base; chemical genetics; circadian behavioral rhythms; circadian pacemaker; fly; insight; interest; novel; null mutation; programs; protein function; research study; response

DESCRIPTION (provided by applicant): We have been studying the molecular control of circadian behavioral rhythms using Drosophila as a model system. Orthologs of genes initially characterized in the fly have now been linked to the control of rhythmic behavior and physiology in vertebrates, including fish, frogs, mice and humans. Here we propose three classes of interdisciplinary investigations of the Drosophila clock. (1) We will conduct collaborative structural studies that can help us determine how specific regulatory actions, previously recognized genetically and biochemically, are performed by certain domains of the PER protein. Does the structure of PER indicate how it interacts with TIM and DBT? Do such data suggest how TIM suppresses PER's phosphorylation by DBT? Does a putative LOV domain near the N-terminus of PER possess a flavin binding domain? (2) We will generate new mutations for the analysis of vital clock genes by Conditional Protein Splicing. Our studies of hyper- and hypo-morphic mutations of GSK-3, dbt, vri, and Pdp-1 indicate that each is a key component of the Drosophila clock. However, because null mutations of these genes are lethal, it has been difficult to determine their full effects on the clock. We are developing a form of chemical genetics in which small diffusible molecules will reversibly control the presence of each vital protein in living flies. (3) We will produce new micro array and statistical approaches to clarify features of rhythmic genome activity and to determine if flies use a single molecular mechanism to generate all circadian rhythms. To begin to link the clock to specific behavioral and physiological outputs, we will investigate a novel set of genes that are regulated by a paired action of light and the circadian clock.

描述（由申请人提供）：我们一直在使用果蝇作为模型系统研究昼夜行为节律的分子控制。最初在果蝇中表征的基因的直系同源物现在已经与脊椎动物（包括鱼、青蛙、小鼠和人类）的节律行为和生理学的控制相关联。在这里，我们提出了三个类的果蝇时钟的跨学科调查。(1)我们将进行合作的结构研究，可以帮助我们确定如何具体的监管行动，以前公认的遗传和生物化学，是由PER蛋白的某些领域进行。PER的结构是否表明它如何与TIM和DBT相互作用？这些数据是否表明TIM如何抑制DBT引起的PER磷酸化？PER N端附近的LOV结构域是否具有黄素结合结构域？(2)我们将通过条件蛋白剪接产生新的突变用于重要时钟基因的分析。我们对GSK-3、dbt、vri和Pdp-1的超型和亚型突变的研究表明，它们都是果蝇生物钟的关键组成部分。然而，由于这些基因的无效突变是致命的，因此很难确定它们对生物钟的全部影响。我们正在开发一种化学遗传学形式，在这种形式中，小的可扩散分子将可逆地控制活体苍蝇中每种重要蛋白质的存在。(3)我们将产生新的微阵列和统计方法，以澄清节律基因组活动的特征，并确定苍蝇是否使用单一的分子机制来产生所有的昼夜节律。为了开始将生物钟与特定的行为和生理输出联系起来，我们将研究一组新的基因，它们受光和生物钟的成对作用的调节。