Jouberin and Nephrocystin in Joubert Syndrome

Jouberin 和肾囊肿素治疗 Joubert 综合征

• 批准号: 8225137
• 负责人: JOSEPH G GLEESON
• 金额: $ 33.1万
• 依托单位: UNIVERSITY OF CALIFORNIA, SAN DIEGO
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-06-01 至 2016-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8225137
• 关键词: Affect; Antibodies; Ataxia; Autistic Disorder; Biochemical; Biological; Biology; Blindness; Brain; Brain Diseases; Cell Culture Techniques; Cell Line; Cells; Cellular Membrane; Cellular biology; Cerebellar Diseases; Childhood; Cilia; Complex; Defect; Development; Digit structure; Disease; Dorsal; Erinaceidae; Event; Eye; Funding; Genes; Genetic; Genetic Models; Goals; Hair; Health; Homeostasis; Human; Incidence; Integral Membrane Protein; Joubert syndrome; Kidney; Kidney Failure; Knock-out; Knockout Mice; Lead; Learning; Life; Liver; Liver Fibrosis; Lung; Magnetic Resonance Imaging; Mediating; Membrane; Mental Retardation; Midbrain structure; Modeling; Monomeric GTP-Binding Proteins; Mus; Mutant Strains Mice; Mutate; Mutation; Nephronophthisis; Neurodevelopmental Disorder; Organ; Pathogenesis; Pathway interactions; Patients; Phosphatidylinositols; Physiological; Plant Roots; Platelet-Derived Growth Factor; Play; Polydactyly; Positioning Attribute; Post-Translational Protein Processing; Pregnancy Outcome; Proteins; Publishing; Regulation; Retinal; Rhodopsin; Role; Signal Pathway; Signal Transduction; Skeletal Muscle; Structure; Structure-Activity Relationship; Technology; Termination of pregnancy; Testing; Tubulin; Work; Zebrafish; base; cellular imaging; ciliopathy; cilium biogenesis; developmental disease; expression vector; fetal; gene function; hindbrain; human disease; improved; kinetosome; mouse model; mutant; nephrogenesis; photoreceptor degeneration; programs; trafficking; unpublished works

DESCRIPTION (provided by applicant): The ciliopathies represent an emerging class of human developmental disorders affecting brain, eye, liver, kidney, digit, skeletal muscle, and lung, all united by disruption of structure or function of the primary cilium. Joubert syndrome (JS) is a ciliopathy, characterized by structural brain anomalies, mental retardation and ataxia, with frequent accompanying retinal blindness, renal failure, polydactyly and hepatic fibrosis. Identifying the pathogenic mechanisms of JS is important for three reasons: 1] A suspicion of a cerebellar disorder frequently leads to pregnancy termination, so understanding these causes can lead to improved predictions about pregnancy outcome. 2] JS has among the highest incidence of co-existent autism among pediatric brain disorders, suggesting what we learn can impact our understanding of more complex disorders. 3] With an improved understanding of basic mechanisms, the field will be in a better position to consider potential treatments. We have identified the genes AHI1, NPHP1, CEP290, ARL13B, and INPP5E as well as several unpublished genes as mutated in patients with JS. We have identified essential signaling functions of these genes in kidney homeostasis, rhodopsin transport, Wnt-, small GTPase-, and phosphatidyl inositol signaling using a combination of mouse modeling, cell biology and biochemical approaches. However, the physiological role of these genes in the pathogenesis of the ciliopathies and the genetic networks remain unknown. The overall goal of this renewal application is to elucidate the developmental, signaling and cell biological mechanisms of the ciliopathy genes underlying the multi- organ involvement in JS, particularly in the context of brain development. We will utilize both traditional and conditional knockout technologies in mouse, genetic modeling in zebrafish, and advanced live-cell imaging capability that will synergize to help advance our understanding of the mechanisms of this important class of disease. PUBLIC HEALTH RELEVANCE: Joubert syndrome is a devastating recessive childhood developmental disorder affecting brain, eye, liver and kidney development, resulting in frequent mental retardation, ataxia, blindness, and renal failure. The underlying causes appear to relate to defects of primary cilia, which are tiny hair-like antennae that extend from most cells. We will study the signaling mechanisms of the genes that others and we have implicated in this disorder in order to understand the basis of these human diseases.

描述（由申请方提供）：纤毛病代表一类影响脑、眼、肝、肾、趾、骨骼肌和肺的新兴人类发育障碍，所有这些疾病均由初级纤毛的结构或功能破坏引起。Joubert综合征（JS）是一种以脑结构异常、智力低下和共济失调为特征的纤毛病，常伴有视网膜盲、肾功能衰竭、多指（趾）畸形和肝纤维化。确定JS的致病机制很重要，原因有三：1）怀疑小脑疾病经常导致妊娠终止，因此了解这些原因可以改善对妊娠结局的预测。2]JS是儿童脑部疾病中共存自闭症发病率最高的疾病之一，这表明我们所学到的东西会影响我们对更复杂疾病的理解。3]随着对基本机制的更好理解，该领域将能够更好地考虑潜在的治疗方法。 我们已经确定了基因AHI 1，NPHP 1，CEP 290，ARL 13 B和INPP 5E以及几个未发表的基因在JS患者中突变。我们已经确定了这些基因在肾脏稳态，视紫红质转运，Wnt-，小GTdR-，和磷脂酰肌醇信号转导的基本信号功能，使用小鼠建模，细胞生物学和生物化学方法的组合。然而，这些基因在纤毛病变的发病机制和遗传网络中的生理作用仍然未知。该更新申请的总体目标是阐明JS中多器官参与的纤毛病基因的发育、信号传导和细胞生物学机制，特别是在脑发育的背景下。我们将在小鼠中利用传统和条件性敲除技术，在斑马鱼中进行遗传建模，以及先进的活细胞成像能力，这些技术将协同作用，帮助我们进一步了解这类重要疾病的机制。 公共卫生相关性：Joubert综合征是一种破坏性的隐性儿童发育障碍，影响脑、眼、肝和肾的发育，导致频繁的智力迟钝、共济失调、失明和肾衰竭。其根本原因似乎与初级纤毛的缺陷有关，初级纤毛是从大多数细胞延伸出来的微小的毛发状触角。我们将研究其他人和我们在这种疾病中涉及的基因的信号机制，以了解这些人类疾病的基础。