The Role of Dscam Dock and Cdc42 Effectors in Prosophilia Neuron Dendritogenesis
The Role of Dscam Dock and Cdc42 Effectors in Prosophilia Neuron Dendritogenesis
批准号:
8702810
负责人:
Bo Huang
金额:
$23.65万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-03-15 至 2016-02-29
关键词:
Adaptor Signaling ProteinBiochemicalBiological AssayBrainCell Adhesion MoleculesCellsCellular StructuresCollectionComplexCouplingCuesCytoskeletonDataData ReportingDendritesDiseaseDown SyndromeDown Syndrome Cell Adhesion MoleculeDrosophila genusEmbryoFamilyFragile X SyndromeGeneticGrowthGrowth ConesGuanosine Triphosphate PhosphohydrolasesImageImaging technologyKnock-outKnowledgeLeadLearningLifeLinkLiteratureMapsMediatingMembraneMethodsMicroscopyMolecularMorphogenesisMorphologyMotor NeuronsNeuraxisNeuronsPathogenesisPathway interactionsPositioning AttributeProteinsRNA InterferenceRegulationResearchResolutionRoleSamplingSignal PathwaySignal TransductionSiteSpecific qualifier valueSystemTestingTimeTranslatingWorkadapter proteinaxon growthbaseextracellularinsightintercellular cell adhesion moleculenetrin receptorneurodevelopmentneuron developmentneuronal circuitryprotein distributionprotein expressionpublic health relevancerhoscreening
中文摘要
描述(由申请人提供):我们的大脑通过相互连接的神经元的复杂和动态网络发挥作用。了解这种神经回路是如何建立和调节的,不仅是神经元发育研究的中心问题,也是了解神经发育障碍发病机制的关键。在果蝇胚胎aCC运动神经元中,我们的初步研究结果暗示了唐氏综合征细胞粘附分子(Dscam 1),细胞骨架活性调节剂,包括Cdc 42效应器,以及树突生长的定位和启动之间的联系。因此,我们假设Dscam细胞间相互作用通过Cdc 42效应子的膜富集促进和定位aCC树突状细胞发生。我们计划使用遗传和超分辨率显微镜方法相结合来测试这一假设。我们的项目包括三个目标:目的1,以检查Cdc 42效应膜积累的作用,在控制新的树突的位置,目的2,以阐明在aCC中的Dscam的机制,以指导Cdc 42效应的定位,目的3,通过Dscam 1-Dscam 1相互作用,了解来自伙伴神经元的细胞外线索。实现这些目标将提供深入了解Dscam功能的详细分子机制,特别是细胞-细胞识别如何通过细胞骨架动力学转化为CNS中的神经元形态发生,这在中枢神经系统(CNS)中一直是非常不足的探索。
英文摘要
DESCRIPTION (provided by applicant): Our brains function through complex and dynamic networks of interconnected neurons. Understanding how this neuronal circuitry is established and regulated is not only the central question of neuron development studies, but also the key to understand the pathogenesis of neurodevelopment disorders. In the aCC motoneuron of Drosophila embryo, our preliminary findings have hinted the connection among the Down syndrome cell adhesion molecule (Dscam1), cytoskeleton activity regulators including Cdc42 effectors, and the positioning and initiating of dendrite growth. Therefore, we hypothesize that Dscam intercellular interaction promotes and positions aCC dendritogenesis through membrane enrichment of Cdc42 effectors. We plan to test this hypothesis using a combination of genetic and super-resolution microscopy methods. Our project consists of three aims: Aim 1 to examine the role of Cdc42 effector membrane accumulation in controlling the position of new dendrites, Aim 2 to elucidate the mechanism for Dscam in aCC to guide the positioning of Cdc42 effectors, and Aim 3 to understand the extracellular cue from partner neurons through Dscam1-Dscam1 interaction. Accomplishing these aims will provide insights into the detailed molecular mechanisms of Dscam function, especially how cell-cell recognition is translated through cytoskeleton dynamics into neuron morphogenesis in CNS, which has been very much under-explored in the central nervous system (CNS).
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Modulation and functional characterization of protein condensation in chromatin organization
-
批准号:10657586
-
项目类别:
-
资助金额:$108.66万
-
财政年份:2020
-
负责人:Bo Huang
-
依托单位:
Modulation and functional characterization of protein condensation in chromatin organization
-
批准号:10264161
-
项目类别:
-
资助金额:$108.66万
-
财政年份:2020
-
负责人:Bo Huang
-
依托单位:
Modulation and functional characterization of protein condensation in chromatin organization
-
批准号:10456148
-
项目类别:
-
资助金额:$108.66万
-
财政年份:2020
-
负责人:Bo Huang
-
依托单位:
Mapping endogenous protein dynamics in living cells
-
批准号:10473533
-
项目类别:
-
资助金额:$28.05万
-
财政年份:2019
-
负责人:Bo Huang
-
依托单位:
Mapping endogenous protein dynamics in living cells
-
批准号:10020992
-
项目类别:
-
资助金额:$28.05万
-
财政年份:2019
-
负责人:Bo Huang
-
依托单位:
Mapping endogenous protein dynamics in living cells
-
批准号:10735776
-
项目类别:
-
资助金额:$34.72万
-
财政年份:2019
-
负责人:Bo Huang
-
依托单位:
Mapping endogenous protein dynamics in living cells
-
批准号:10242797
-
项目类别:
-
资助金额:$28.05万
-
财政年份:2019
-
负责人:Bo Huang
-
依托单位:
Structure mapping of molecular complexes by super-resolution microscopy
-
批准号:9902489
-
项目类别:
-
资助金额:$34.28万
-
财政年份:2018
-
负责人:Bo Huang
-
依托单位:
Rapid screening of gene-edited cells
-
批准号:9751906
-
项目类别:
-
资助金额:$20.06万
-
财政年份:2018
-
负责人:Bo Huang
-
依托单位:
Multimerized GFP probe for live cell imaging
-
批准号:9169444
-
项目类别:
-
资助金额:$23.78万
-
财政年份:2016
-
负责人:Bo Huang
-
依托单位:
Multimerized GFP probe for live cell imaging
-
批准号:9275525
-
项目类别:
-
资助金额:$19.81万
-
财政年份:2016
-
负责人:Bo Huang
-
依托单位:
Analyzing genomic elements in live animals by CRISPR imaging
-
批准号:8934113
-
项目类别:
-
资助金额:$39.63万
-
财政年份:2014
-
负责人:Bo Huang
-
依托单位:
Analyzing genomic elements in live animals by CRISPR imaging
-
批准号:8832139
-
项目类别:
-
资助金额:$34.36万
-
财政年份:2014
-
负责人:Bo Huang
-
依托单位:
Solving macromolecular complex architecture in situ by super-resolution microscop
-
批准号:8146140
-
项目类别:
-
资助金额:$231.75万
-
财政年份:2011
-
负责人:Bo Huang
-
依托单位:
海外基金