Engrailed targets and the control of synaptic circuits in Drosophila
果蝇的纠缠目标和突触回路的控制
基本信息
- 批准号:8657495
- 负责人:
- 金额:$ 37.13万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2012
- 资助国家:美国
- 起止时间:2012-05-01 至 2016-04-30
- 项目状态:已结题
- 来源:
- 关键词:AdultAfferent NeuronsAnimalsAuditoryAuditory systemAutistic DisorderAutomobile DrivingAxonBindingBiological AssayBiological ModelsBrainBranchiostoma floridae AmphiEn proteinCell Adhesion MoleculesCell surfaceCouplingCulicidaeDataDatabasesDengueDevelopmentDiseaseDisease VectorsDrosophila genusDrosophila melanogasterElectrophysiology (science)EnsureEvolutionFiberGene TargetingGenesGoalsHealthHumanInsectaKnock-outKnockout MiceKnowledgeLabelLeucine-Rich RepeatLinkMalariaMammalsMeasuresMethodsMidbrain structureModelingMolecularMorphologyNeuraxisNeuronsParkinson DiseasePartner in relationshipPathway interactionsPatternPilot ProjectsPlayPositioning AttributeProcessProtein OverexpressionProteinsRNA InterferenceRegulationRepressionResearchRoleSpecificitySymptomsSynapsesSystemTestingautism spectrum disorderaxon guidanceaxonal guidanceaxonal pathfindingconnectindesigndisorder controldopaminergic neuronfeedingflyhuman diseaseinnovationknock-downmembernervous system disorderneural circuitneurobiotinneuroglianneuron developmentneuronal survivaloverexpressionsynaptogenesistranscription factorvisual stimulus
项目摘要
DESCRIPTION (provided by applicant): Engrailed (En) is a transcription factor first discovered in Drosophila but later found to be present in all animals, playing an important role in controllin neuronal development. Little is known about the cell surface molecules that it regulates. The long-term goal of this research is to find out how En regulates synaptic connectivity in the CNS, with a particular focus on identifying and characterizing its target genes of cell surface effector
molecules. Preliminary data show that overexpression of En in Drosophila olfactory neurons alters their axonal path finding to their targets, the olfactory glomeruli. Additionally, ectopic E expression in a normally En- negative subset of auditory neurons allows them to form synaptic connections with the Giant Fiber (GF) escape neuron. The first aim is to selectively knock out En in olfactory neurons using fly lines in which RNAi is driven by the Gal4-UAS system. I will determine the effects on axonal guidance by assaying changes in the morphology of GFP-labeled olfactory axons, and alterations in the positions of immunolabeled olfactory glomeruli. The second aim will drive En RNAi in the auditory neurons and measuring their synaptic input to the GF. The third aim is to test whether increasing or knocking down expression of the En target Connectin, a member of the conserved LRR superfamily of adhesion molecules, alters axon guidance or glomerulus positioning. I will also test whether En knockout results in overexpression of this protein, as would be expected if it is a target of En repression. In the finl aim, I will ectopically express or knock down the En-binding target gene Neuroglian, a cell surface adhesion molecule homologous to vertebrate L1-CAM, then use the auditory synapse assays of connection to the GF. I will also test whether its immunostaining is altered by overexpression or knockout of En, as would be expected if it is negatively regulated by En. Relevance: En has been shown to control the survival of midbrain dopaminergic neurons, with En knockout mice showing Parkinson-like symptoms, and it has also been linked to autism spectrum disorder. Drosophila models are particularly useful for the discovery of molecular pathways that are directly relevant to human health, because most of these pathways have been conserved during evolution. All animals have En protein, so it is very likely that any molecules that are regulated by it during the process of synapse formation in Drosophila have their counterparts in humans, playing similar roles. These molecules may be of great potential importance in neurological diseases such as Parkinson's or autism. In addition, the basic knowledge gained from this project about the development of dipteran olfactory and auditory systems could be of use in designing ways to disrupt the feeding and mating patterns of mosquitoes, which are vectors of diseases such as malaria and dengue fever.
描述(由申请人提供):Engrailed (En)是一种转录因子,最早在果蝇中发现,后来发现在所有动物中都存在,在控制神经元发育中起重要作用。人们对它所调节的细胞表面分子知之甚少。本研究的长期目标是发现En如何调节中枢神经系统的突触连通性,重点是识别和表征其细胞表面效应靶基因
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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JONATHAN M BLAGBURN其他文献
JONATHAN M BLAGBURN的其他文献
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{{ truncateString('JONATHAN M BLAGBURN', 18)}}的其他基金
Engrailed and the control of synaptic circuits in adult Drosophila
成年果蝇的 Engrailed 和突触回路的控制
- 批准号:
9922928 - 财政年份:2017
- 资助金额:
$ 37.13万 - 项目类别:
Engrailed targets and the control of synaptic circuits in Drosophila
果蝇的纠缠目标和突触回路的控制
- 批准号:
8468764 - 财政年份:2012
- 资助金额:
$ 37.13万 - 项目类别:
Engrailed targets and the control of synaptic circuits in Drosophila
果蝇的纠缠目标和突触回路的控制
- 批准号:
8843056 - 财政年份:2012
- 资助金额:
$ 37.13万 - 项目类别:
Engrailed targets and the control of synaptic circuits in Drosophila
果蝇的纠缠目标和突触回路的控制
- 批准号:
8257801 - 财政年份:2012
- 资助金额:
$ 37.13万 - 项目类别:
Engrailed and the Control of Synaptic Circuitry in Drosophila
果蝇的纠缠和突触回路的控制
- 批准号:
7497678 - 财政年份:2008
- 资助金额:
$ 37.13万 - 项目类别:
Engrailed and the Control of Synaptic Circuitry in Drosophila
果蝇的纠缠和突触回路的控制
- 批准号:
7683182 - 财政年份:2008
- 资助金额:
$ 37.13万 - 项目类别:
Engrailed and the Control of Synaptic Circuitry in Drosophila
果蝇的纠缠和突触回路的控制
- 批准号:
7896492 - 财政年份:2008
- 资助金额:
$ 37.13万 - 项目类别:
DEVELOPMENT OF SYNAPSES BETWEEN IDENTIFIED NEURONS
已识别神经元之间突触的发育
- 批准号:
6496791 - 财政年份:2001
- 资助金额:
$ 37.13万 - 项目类别:
DEVELOPMENT OF SYNAPSES BETWEEN IDENTIFIED NEURONS
已识别神经元之间突触的发育
- 批准号:
6338922 - 财政年份:2000
- 资助金额:
$ 37.13万 - 项目类别:
DEVELOPMENT OF SYNAPSES BETWEEN IDENTIFIED NEURONS
已识别神经元之间突触的发育
- 批准号:
6273599 - 财政年份:1998
- 资助金额:
$ 37.13万 - 项目类别:
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