Wnt signaling via the Drl axon guidance receptor
Wnt signaling via the Drl axon guidance receptor
批准号:
7276031
负责人:
Renee D Read
金额:
$5.04万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-09-30 至 2008-09-29
关键词:
AxonBinding ProteinsBiologicalBiological AssayCellsCuesCytoplasmic TailDevelopmentDiseaseDrosophila genusEventFamilyGeneticGoalsHumanInvestigationLigandsMalignant NeoplasmsMapsMolecularNeoplasm MetastasisNeuronsOrthologous GenePathway interactionsProcessProtein FamilyProteolysisProteomicsReceptor Protein-Tyrosine KinasesRoleSignal PathwaySignal TransductionStructureSynapsesWnt proteinsaxon guidancecancer cellcell motilityin vivomemberreceptorresponse
中文摘要
描述(由申请人提供):生长中的神经元必须通过感知调节细胞运动的引导信号来识别和遵循特定的突触目标通路。在果蝇中,Drl受体由一部分神经元表达,是轴突寻路所必需的。Drl是非典型受体酪氨酸激酶(RTKs) Ryk家族的成员,RTKs是Wnt配体的催化无活性受体。Wnt配体通常在不同于rtk的信号通路中起作用,参与多种疾病过程,如癌细胞侵袭和转移。人类Drl的同源基因Ryk也与许多癌症有关。然而,对于Ryk家族受体响应wnt所启动的信号事件知之甚少。本提案的更广泛目标是识别和表征Drl和Wnt蛋白调节细胞运动的信号通路。研究人员将利用蛋白质组学、细胞生物学和遗传学方法来阐明Drl的信号活性:1)分析Drl细胞质结构域的功能区域;2)研究Drl膜内蛋白水解的作用和释放的Drl细胞质结构域的功能;3)鉴定Drl结合蛋白;4)表征Drl结合蛋白和候选Drl信号效应物。
英文摘要
DESCRIPTION (provided by applicant): Growing neurons must recognize and follow specific pathways to their synaptic targets by sensing guidance cues that regulate cell motility. In Drosophila, the Drl receptor is expressed by a subset of neurons and is required for proper axon pathfinding. Drl is a member of the Ryk family of atypical receptor tyrosine kinases (RTKs), which are catalytically inactive receptors for Wnt ligands. Wnt ligands, which typically function in signaling pathways distinct from RTKs, are involved in multiple disease processes such as cancer cell nvasiveness and metastasis. The human Drl ortholog, Ryk, has also been implicated in numerous cancers. Yet, little is known about the signaling events initiated by Ryk family receptors in response to Wnts. The broader goal of this proposal is to identify and characterize the signaling pathways employed by Drl and Wnt proteins to regulate cell motility. Drl signaling activity will be elucidated using proteomic, cell-biological, and genetic approaches to 1) Analyze the Drl cytoplasmic domain for functional regions, 2) Investigate the role Drl ntramembrane proteolysis and the function of the released Drl cytoplasmic domain, 3) Identify Drl binding proteins, and 4) Characterize Drl-binding proteins and candidate Drl signaling effectors.
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海外基金