GAPs in Signaling to the Spine and Retardation: Mechanisms and the Role of WRP

脊柱信号传递中的差距和发育迟缓：机制和 WRP 的作用

• 批准号: 8215795
• 负责人: SCOTT H SODERLING
• 金额: $ 33.44万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-02-01 至 2013-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8215795
• 关键词: Actins; Address; Affect; Animals; Behavior; Behavior assessment; Behavioral; Binding; Binding Proteins; Biochemical; Biological Assay; Cell membrane; Cell physiology; Cells; Cellular Assay; Cellular biology; Clathrin; Clathrin-Coated Vesicles; Cognition; Cognitive; Complement; Core Facility; Critiques; Cytoskeleton; Data; Databases; Defect; Deletion Mutagenesis; Dendritic Spines; Development; Endocytosis; Etiology; Excitatory Synapse; Exhibits; Fluorescence Resonance Energy Transfer; GTPase-Activating Proteins; Gene Mutation; General Population; Genes; Glutamate Receptor; Goals; Grant; Guanine Nucleotide Exchange Factors; Guanosine Triphosphate; Health; Human; Hydrolysis; Image; Impaired cognition; In Vitro; Individual; Knock-out; Knockout Mice; Knowledge; Lead; Learning; Light; Link; Lipid Binding; Lipids; Literature; Measures; Mediating; Membrane; Memory; Mental Retardation; Microscopy; Mission; Molecular; Monitor; Morphology; Mus; Mutation; N-terminal; Neurites; Neuronal Dysfunction; Neurons; Pathway interactions; Patients; Phenotype; Phosphatidylinositol 4,5-Diphosphate; Phosphatidylinositols; Physiological; Play; Preparation; Principal Investigator; Protein Binding; Proteins; Reagent; Recruitment Activity; Regulation; Research; Role; Signal Pathway; Signal Transduction; Signaling Protein; Site; Specificity; Structure; Surface; Synapses; Synaptic plasticity; TRIP10 gene; Testing; Total Internal Reflection Fluorescent; Transgenic Mice; United States National Institutes of Health; Universities; Vertebral column; WAVE protein; Work; base; behavioral impairment; chromosome 3p deletion syndrome; design; experience; in vivo; interdisciplinary approach; member; mouse model; mutant; nervous system disorder; neuropathology; novel; positional cloning; proband; programs; protein function; receptor; research study; rho; rho GTP-Binding Proteins; rho GTPase-activating protein; synaptic function; tool; trafficking

DESCRIPTION (provided by applicant): Several genes implicated in neurological disease are thought to regulate Rho GTPase signaling, yet there is a limited understanding of how these signaling proteins function. WRP (WAVE associated Rac GAP protein), which was identified by positional cloning as a gene disrupted in 3p-syndrome mental retardation (MR), is one such protein. WRP regulates actin remodeling by binding to the Rac effector WAVE-1 and by stimulating Rac GTP hydrolysis. WAVE-1 null mice exhibit dramatic behavioral impairments in learning and memory tests. Importantly, the phenotype of WAVE-1 null mice overlaps well with those of 3p-syndrome retardation, supporting a link between WRP regulated signaling and MR. The objective of this application is to examine the molecular mechanisms regulating WRP and whether loss of WRP affects specific neuronal functions that contribute to behavioral impairments. Our central hypothesis is that one cellular function of WRP is to regulate actin signaling in spines. Thus loss of WRP would lead to spine abnormalities and cognitive impairments. This hypothesis is guided by strong preliminary data based on 1) structure/function and imaging data defining a WRP targeting domain and 2) data linking WRP and WAVE-1 to spinogenesis, synaptic plasticity and cognitive behavior. The specific aims of this grant are: 1) Identify the mechanisms that spatially target and regulate WRP. We will use a combination of biochemical and imaging approaches designed to address how WRP is regulated and may be targeted to subcellular compartments. 2) Delineate the cellular role of anchored WRP. Because WRP regulates Rac and WAVE-1, we hypothesize targeting of WRP is a salient feature of this signaling pathway in spines. We will use imaging and cellular assays to quantify the role of WRP targeting in synapse function. 3) Test the in vivo function of WRP in regulating cognitive behavior and synapse function. Using a conditional WRP null mouse model we will analyze aspects of synapse function in vivo and in vitro. We will also examine these mice for abnormalities in a range of behaviors related to 3p-syndrome retardation. Because this proposal utilizes a multidisciplinary approach to analyze WRP signaling, a fundamental advance in understanding the mechanisms linking actin signaling to neuronal dysfunction can be anticipated. PUBLIC HEALTH RELEVANCE: This research is relevant to the mission of NIH because it examines the functional role of a gene implicated in mental retardation at the molecular, cellular and organismal level. Thus, important advances in understanding the etiology of mental retardation could be anticipated. It is also expected that knowledge gained in these studies will shed light on other forms of neuropathologies that involve abnormal Rho-GTPase signaling and mechanisms that normally regulate neuronal connectivity.

描述（由申请人提供）：一些与神经系统疾病相关的基因被认为调节Rho GTPase信号传导，但对这些信号传导蛋白如何发挥作用的理解有限。WRP （WAVE相关Rac GAP蛋白）就是这样一种蛋白，它被定位克隆鉴定为在3p综合征精神发育迟滞（MR）中被破坏的基因。WRP通过结合Rac效应物WAVE-1和刺激Rac GTP水解来调节肌动蛋白重塑。WAVE-1无效小鼠在学习和记忆测试中表现出明显的行为障碍。重要的是，WAVE-1缺失小鼠的表型与3p综合征迟缓小鼠的表型重叠良好，支持WRP调节信号与mr之间的联系。本应用的目的是研究WRP调节的分子机制，以及WRP缺失是否影响导致行为障碍的特定神经元功能。我们的中心假设是，WRP的一个细胞功能是调节脊髓中的肌动蛋白信号。因此，WRP的缺失会导致脊柱异常和认知障碍。这一假设得到了强有力的初步数据的指导：1)结构/功能和成像数据定义了WRP靶向域；2)将WRP和WAVE-1与脊髓发生、突触可塑性和认知行为联系起来的数据。该赠款的具体目标是：1)确定在空间上瞄准和调节WRP的机制。我们将使用生化和成像方法的结合，旨在解决WRP是如何调节的，并可能针对亚细胞区室。2)描述锚定WRP在细胞中的作用。由于WRP调节Rac和WAVE-1，我们假设WRP的靶向性是脊髓中这一信号通路的一个显著特征。我们将使用成像和细胞分析来量化WRP靶向在突触功能中的作用。3)测试WRP在体内调节认知行为和突触功能的功能。使用条件WRP null小鼠模型，我们将分析体内和体外突触功能的各个方面。我们还将检查这些小鼠的一系列与3p综合征发育迟缓相关的行为异常。由于该建议采用多学科方法分析WRP信号，因此可以预期在理解肌动蛋白信号传导与神经元功能障碍之间的机制方面取得根本性进展。公共卫生相关性：这项研究与美国国立卫生研究院的使命相关，因为它在分子、细胞和有机体水平上检查了与智力迟钝有关的基因的功能作用。因此，在理解智力迟钝的病因方面的重要进展是可以预期的。我们还期望在这些研究中获得的知识将揭示涉及异常Rho-GTPase信号传导和正常调节神经元连接机制的其他形式的神经病理学。