MOLECULAR STUDIES OF PRIMARY CILIUM BIOGENESIS

原代纤毛生物发生的分子研究

• 批准号: 8050032
• 负责人: Maxence V Nachury
• 金额: $ 30.89万
• 依托单位: STANFORD UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2010
• 资助国家: 美国
• 起止时间: 2010-04-01 至 2015-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8050032
• 关键词: Award; Bardet-Biedl Syndrome; Binding; Binding Proteins; Biochemical; Biological Assay; Cell Polarity; Cell model; Cell surface; Cells; Cilia; Clathrin; Clathrin Adaptors; Clinical; Coat Protein Complex I; Complex; Cystic kidney; Cytoplasmic Tail; Data; Defect; Disease; Docking; Erinaceidae; Etiology; Functional disorder; Goals; Growth; Guanine Nucleotide Exchange Factors; Guanosine Triphosphate Phosphohydrolases; Health; Hepatic; Hereditary Disease; Hydrolysis; Inborn Genetic Diseases; Individual; Integral Membrane Protein; Lead; Mediating; Membrane; Membrane Proteins; Modality; Modeling; Molecular; Names; Nucleotides; Obesity; Organ; Output; Polycystic Kidney Diseases; Property; Protein translocation; Proteins; Reaction; Receptor Signaling; Recruitment Activity; Research; Research Proposals; Retinal Degeneration; Role; Signal Pathway; Signal Transduction; Sorting - Cell Movement; Surface; Symptoms; Testing; Time; United States National Institutes of Health; Variant; Vesicle; Weight; base; cilium biogenesis; insight; polymerization; public health relevance; reconstitution; research study; skeletal abnormality; therapeutic development; trafficking

DESCRIPTION (provided by applicant): The primary cilium, a "signaling antenna" projecting at the surface of the cell, is required for the transduction of Hedgehog and planar cell polarity signals and concentrates many signaling receptors on its surface. Furthermore, ciliary dysfunction leads to obesity, retinal degeneration and kidney cysts in the inherited disorder Bardet-Biedl Syndrome (BBS). Yet, the mechanisms of signaling receptor trafficking to the ciliary membrane are not understood. We recently discovered a stable complex of seven BBS proteins, that we named the BBSome and have implicated in vesicular trafficking to the cilium based on its functional interaction with Rab8, a GTPase with a well-established trafficking function whose manipulations directly impact cilium growth. Here, we advance the hypothesis that the BBSome sorts specific transmembrane proteins to the primary cilium. In this research proposal, we will dissect BBSome function within the context of vesicular transport to the cilium through the following aims: 1- Identify the transmembrane proteins transported by the BBSome towards the cilium. Known ciliary transmembrane proteins will be tested for a BBSome requirement in their trafficking to cilia and we will establish a time-resolved trafficking assay to identify the donor compartment from which the BBSome selects its cargoes. 2- Dissect the mechanisms of BBSome targeting to cilia. We will assay the function of BBSome-binding proteins in mediating the recruitment of the BBSome to cilia. 3- Characterize the functional interplay between the BBSome and Rab8. In preliminary studies, we have found that the BBSome interacts with Rabin8, the GDP/GTP exchange factor for Rab. Here, we will seek to understand how the BBSome modulates the activity and localization of Rabin8 to enable Rab8 entry into the cilium. In conclusion, our model for BBSome function has significant implications for the etiology of Bardet-Biedl syndrome: in a model where the BBSome targets specific signaling receptors to the cilium, each individual symptom of BBS results from the disruption of a specific ciliary signaling pathway. PUBLIC HEALTH RELEVANCE: Anomalies of the primary cilium underly the etiology of polycystic kidney disease, the most frequent autosomal dominant hereditary disorder. More broadly, cilia are thought to represent the unifying causality for a class of disorders presenting with obesity, skeletal abnormalities and retinal degeneration. Thus, gaining an understanding of the basic mechanisms that build the primary cilium has the potential to further our understanding of numerous clinical modalities and possibly lead to the development of therapeutics for multiple indications.

描述（由申请人提供）：初级纤毛是突出在细胞表面的“信号天线”，是转导Hedgehog和平面细胞极性信号所必需的，并且在其表面上集中了许多信号受体。此外，在遗传性疾病Bardet-Biedl综合征（BBS）中，睫状体功能障碍导致肥胖、视网膜变性和肾囊肿。然而，信号受体运输到睫状膜的机制尚不清楚。我们最近发现了一个稳定的复合物的七个BBS蛋白，我们命名为BBSome和有牵连的泡状贩运纤毛的基础上，其功能相互作用与Rab 8，一个GTlymphocyte与一个完善的贩运功能，其操作直接影响纤毛的生长。在这里，我们提出的假设，BBSome排序特定的跨膜蛋白的初级纤毛。在这项研究计划中，我们将通过以下目标在泡状运输到纤毛的背景下解剖BBSome功能：1-鉴定BBSome向纤毛运输的跨膜蛋白。将测试已知的纤毛跨膜蛋白在其运输到纤毛中的BBSome要求，并且我们将建立时间分辨运输测定以鉴定BBSome从中选择其货物的供体隔室。2-探讨BBSome靶向纤毛的作用机制。我们将分析BBSome-binding蛋白在介导BBSome-cilia募集中的功能。3-描述BBSome和Rab 8之间的功能相互作用。在初步研究中，我们发现BBSome与Rabin 8相互作用，Rabin 8是Rab的GDP/GTP交换因子。在这里，我们将试图了解BBSome如何调节Rabin 8的活性和定位，使Rab 8进入纤毛。总之，我们的BBSome功能模型对Bardet-Biedl综合征的病因学具有重要意义：在BBSome靶向纤毛特异性信号受体的模型中，BBS的每个个体症状都是由特定纤毛信号通路的破坏引起的。 公共卫生相关性：原发纤毛异常是多囊肾病的病因学基础，多囊肾病是最常见的常染色体显性遗传病。更广泛地说，纤毛被认为代表了一类表现为肥胖、骨骼异常和视网膜变性的疾病的统一因果关系。因此，了解建立初级纤毛的基本机制有可能进一步了解许多临床模式，并可能导致多种适应症的治疗方法的发展。