Neuronal function of huntingtin associated protein
亨廷顿相关蛋白的神经元功能
基本信息
- 批准号:7371939
- 负责人:
- 金额:$ 33.47万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1998
- 资助国家:美国
- 起止时间:1998-01-01 至 2011-11-30
- 项目状态:已结题
- 来源:
- 关键词:14-3-3 ProteinsART proteinATP phosphohydrolaseAdaptor Signaling ProteinAddressAdenovirus VectorAdenovirusesAdultAffectAfferent NeuronsAgeAlanineAllelesAlternative SplicingAmino AcidsAmygdaloid structureAnimal BehaviorAnimal ModelAnimalsAntibodiesAntigensAprotininAreaAxonAxonal TransportBacteriaBehavioralBilateralBindingBinding SitesBiochemicalBiologicalBiological AssayBiotinBiotinylationBirthBody SizeBody WeightBody Weight decreasedBrainBrain regionBrain-Derived Neurotrophic FactorBreedingBuffersBypassC-terminalCalcium/calmodulin-dependent protein kinaseCaliforniaCatalytic DomainCause of DeathCaviaCell CountCell FractionCell FractionationCell NucleusCell SurvivalCell membraneCell modelCell physiologyCell surfaceCellsCentrifugationCessation of lifeChimeric ProteinsCleaved cellCloningCodeCollaborationsComplementary DNAComplexComputer softwareConditionConfocal MicroscopyContralateralCorpus striatum structureCulture MediaCultured CellsCyclic AMPCyclic AMP-Dependent Protein KinasesCytolysisCytomegalovirusCytoplasmCytoplasmic InclusionCytosolDataDefectDensitometryDependovirusDepthDietDiffuseDigestionDiseaseDisruptionDistalDrosophila genusDyesDynein ATPaseES Cell LineEatingEating BehaviorEgtazic AcidElectron MicroscopyEmployee StrikesEndocytosisEndosomesEnsureEpidermal Growth FactorEpidermal Growth Factor ReceptorEpitopesEquilibriumEventExonsFamilyFc ReceptorFeeding behaviorsFemaleFetusFigs - dietaryFluorescenceFluorescence Recovery After PhotobleachingFluorescent DyesFoodForelimbFractionationFreezingFunctional disorderFundingFutureGABA ReceptorGamma counterGene TargetingGenerationsGenesGeneticGenetic RecombinationGenomicsGenotypeGillsGlassGluesGlutamatesGlutamineGlutathioneGlutathione S-TransferaseGlycerophosphatesGoalsGolgi ApparatusGrantGreen Fluorescent ProteinsGrowthGrowth Factor ReceptorsHandHarvestHeadHindlimbHippocampus (Brain)Homologous GeneHumanHuman Amyloid Precursor ProteinHuntington DiseaseHypothalamic structureIceImageImage AnalysisImmunoblottingImmunoglobulin GImmunoprecipitationImpairmentIn VitroIncubatedIndividualInfectionInjection of therapeutic agentInositolInstitutesIntakeIntracellular TransportInvestigationJapanKetamineKinesinKineticsKnock-in MouseKnock-outKnockout MiceLabelLaboratoriesLeadLeftLengthLettersLeupeptinsLifeLigand BindingLigandsLigationLigatureLightLinkLocalizedLong-Term EffectsLysineLysosomesMammalian CellManuscriptsMasksMeasurementMeasuresMediatingMediator of activation proteinMedicineMembraneMembrane Protein TrafficMembrane ProteinsMemory LossMethodsMicroinjectionsMicroscopeMicroscopyMicrotubulesMitochondriaModelingMolecularMonitorMonoclonal AntibodiesMorphologyMotorMotor Neuron DiseaseMotor NeuronsMovementMovement DisordersMultivesicular BodyMusMutateMutationN-terminalNGFR ProteinNatureNeomycinNeomycin resistance geneNerveNerve DegenerationNerve Growth FactorsNeuraxisNeuritesNeuritisNeurodegenerative DisordersNeurogliaNeurologicNeurologistNeuronal DifferentiationNeuronal DysfunctionNeuronsNeurosciencesNeurotrophic Tyrosine Kinase Receptor Type 1Newborn AnimalsNonidet P-40NuclearNumbersNycomedOkadaic AcidOrganellesOryctolagus cuniculusOutcomePC12 CellsPKA inhibitorPOMC genePaperPartner in relationshipPathogenesisPathologyPathway interactionsPatientsPeptidesPeripheralPersonal SatisfactionPharmaceutical PreparationsPhenotypePhiladelphiaPhosphate BufferPhosphoric Monoester HydrolasesPhosphorylationPhosphorylation SitePhosphotransferasesPhotobleachingPlasmidsPlayPolymerase Chain ReactionPost-Translational Protein ProcessingPrecipitationPreparationPrincipal InvestigatorPro-OpiomelanocortinProceduresProcessProgress ReportsPromegaProtein BindingProtein ConformationProtein IsoformsProtein Kinase Protein PhosphorylationProtein OverexpressionProteinsProto-Oncogene Proteins c-aktProtocols documentationPublicationsPublishingPurposeRateRattusReactionReagentReceptor SignalingRecombinant ProteinsRecoveryRecyclingRegulationRelative (related person)ReporterReportingResearchResearch PersonnelResolutionRight-OnRodentRoleRotarod Performance TestSamplingScaffolding ProteinScreening procedureSerineSerum-Free Culture MediaSignal PathwaySignal TransductionSignaling MoleculeSiteSite-Directed MutagenesisSlideSmall Interfering RNASolidSolutionsSouthern BlottingSpecificitySpinal GangliaStagingStaining methodStainsStandards of Weights and MeasuresStaurosporineStreptavidinStretchingStrokeStructureStructure of nucleus infundibularis hypothalamiSubcellular FractionsSubcellular structureSucroseSurfaceSymptomsSynaptic VesiclesSystemTailTestingTexas redThalamic structureThigh structureThinkingThreonineThymidine KinaseTimeTissuesToxic effectTracerTransfectionTransferrinTransgenesTransgenic MiceTransgenic OrganismsTransport VesiclesTrkA proteinTubulinUnited States National Institutes of HealthVertebratesVesicleViralViral VectorVirusVirus DiseasesWaterWater consumptionWeekWestern BlottingWild Type MouseWorkYangYeastsanaloganterograde transportantibody conjugatebasebiotin 1blastocystbrain tissuecalmodulin-dependent protein kinase IIcell growth regulationcell typecellular pathologycryostatcytotoxicitydaydesigndimerdosagedynactindynactin 1embryonic stem cellenolaseexperiencefactor Afeedingfluorescence imaginggain of functionganghomologous recombinationhuman APEX1 proteinhuman Huntingtin proteinhuman diseaseimmunocytochemistryimmunoreactionin vivoinsightinstrumentinterestintracellular protein transportknock-downleupeptinloss of functionmalemicrobial alkaline proteinase inhibitormouse Hap1 proteinmouse modelmoviemutantneuronal cell bodyneuronal survivalneuronal transportneuropathologyneuropeptide Y2 receptorneurotoxicitynumb proteinparticlephosphatase inhibitorplasmid DNApolyclonal antibodypolyfunctional aziridinepolyglutaminepolypeptidepostnatalprogramspromoterprotein aggregationprotein transportpuprat Hap1 proteinreceptorreceptor expressionreceptor functionreceptor internalizationreceptor recyclingrecombinaserelating to nervous systemresearch studyresponseretrograde transportsample fixationsciatic nervesulfo-N-hydroxysuccinimide-biotinsynaptic functiontheoriestraffickingtranscriptional coactivator p75transmission processtrendtripolyphosphatetyrosine kinase ABL1vectorxylamineyeast two hybrid system
项目摘要
Huntingtin associated protein-1 (HAP1) is enriched in neurons and is found to be involved in
intracellular trafficking. The role of HAP1 in intracellular trafficking is supported by its interactions with a
number of proteins including dynactin p150 and kinesin, which are involved in microtubule-dependent
transport. Recent studies also suggest that HAP1 participates in vesicular trafficking and endocytosis
of membrane receptors. The crucial function of HAP1 was further demonstrated by HAP1 knockout
mice that are pbstnatally lethal and show neurodegeneration in the brain. These interesting findings
raise more questions about how HAP1 is involved in the complex intracellular trafficking in neurons.
Our recent studies show that HAP1 interacts with 14-3-3 and that this interaction is regulated by
phosphorylation of HAP1. We hypothesize that HAP1 may link specific cargos to the microtubule
transporters and that it's interactions with partners are regulated by its posttranslational modifications.
Such regulation allows HAP1 to participate in intracellular transport of various cargos and endocytosis
of membrane receptors. Given the idea that HAP1 dysfunction may be involved in HD pathology, it is
also important to investigate if the loss of HAP1 can affect its function in intracellular trafficking.
Accordingly, we propose three aims in this application. In Aim 1, we will investigate whether 14-3-3 and
phosphorylation regulate the interactions of HAP1 with microtubule transporters dynactin p150and
kinesin. In Aim-2, we will use HAP1 knockout mice and siRNA approaches to examine whether
decreasing MAPI's expression alters microtubule-dependent transport and neuronal function in
different types of neurons. In Aim-3, we will study whether HAP1 deficiency affects endocytosis of
membrane receptors and whether defective HAP1-associated endocytosis contributes to HD
pathology. These studies aim to elucidate the function of HAP1 and to help understand the
mechanisms for intracellular trafficking in neurons.
Huntingtin相关蛋白-1(HAP1)富含神经元,发现与
细胞内贩运。 HAP1在细胞内运输中的作用得到了其与A的相互作用的支持
依赖微管涉及的蛋白质数量在内
运输。最近的研究还表明,HAP1参与囊泡贩运和内吞作用
膜受体。 HAP1敲除进一步证明了HAP1的关键功能
pBstnatial致死并在大脑中显示神经退行性的小鼠。这些有趣的发现
关于HAP1如何参与神经元中复杂的细胞内贩运方式提出了更多问题。
我们最近的研究表明,HAP1与14-3-3相互作用,并且这种相互作用受
HAP1的磷酸化。我们假设HAP1可以将特定的嘉戈斯连接到微管
转运蛋白及其与合作伙伴的互动受其翻译后修饰的调节。
这种调节允许HAP1参与各种尸体和内吞作用的细胞内转运
膜受体。鉴于HAP1功能障碍可能与HD病理有关的想法,这是
研究HAP1是否会影响其在细胞内运输中的功能也很重要。
因此,我们在此应用中提出了三个目标。在AIM 1中,我们将调查14-3-3和
磷酸化调节HAP1与微管转运蛋白Dynactin P150和
动力学。在AIM-2中,我们将使用HAP1敲除小鼠和siRNA方法来检查是否是否
减少MAPI的表达会改变微管依赖性转运和神经元功能
不同类型的神经元。在AIM-3中,我们将研究HAP1缺乏症是否影响
膜受体以及有缺陷的HAP1相关内吞作用是否有助于HD
病理。这些研究旨在阐明HAP1的功能,并帮助了解
神经元细胞内贩运的机制。
项目成果
期刊论文数量(0)
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XIAO-JIANG LI其他文献
XIAO-JIANG LI的其他文献
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{{ truncateString('XIAO-JIANG LI', 18)}}的其他基金
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