The Role of Sam68 in Synaptic Transmission and Plasticity
The Role of Sam68 in Synaptic Transmission and Plasticity
批准号:
8061082
负责人:
Matthew Klein
金额:
$4.68万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-12-21 至 2014-05-20
关键词:
AcuteAddressAffectAnimalsAtaxiaBrainCellsCerebellumCommunicationDendritic SpinesDisciplineDiseaseElectrophysiology (science)EnsureFMRPFamilyFamily memberFluorescent in Situ HybridizationFragile X SyndromeFunctional disorderGlutamate ReceptorGoalsHippocampus (Brain)ImmunohistochemistryInjection of therapeutic agentInvestigationJordanKH DomainKnock-outKnockout MiceLaboratoriesLearningLinkMeasuresMediatingMentorshipMessenger RNAMolecularMolecular BiologyMuscleMutationN-Methyl-D-Aspartate ReceptorsNeuraxisNeuronsNeurosciencesPathogenesisPathway interactionsProtein BiosynthesisProtein FamilyProteinsPsyche structureRNA-Binding ProteinsRattusReporterResearch PersonnelRoleSRC-associated p68 proteinSchizophreniaSliceSpinalSpinal Muscular AtrophySubfamily lentivirinaeSurfaceSynapsesSynaptic TransmissionSynaptic plasticityTechniquesTrainingTranslationsTremorTremor/Ataxia SyndromeUntranslated RegionsViralexperiencein vivoinsightinterdisciplinary approachknock-downmembernervous system disorderneurotransmissionnovelpatch clampreceptorresearch studyskillssmall hairpin RNAsrc-Family Kinasessynaptic functiontherapy developmenttrafficking
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The goal of this project is to describe a novel role for the RNA-binding protein Sam68 in synaptic transmission and plasticity. Sam68 is a member of the KH-domain containing family of proteins, which have been linked to the pathogenesis of several neurological disorders via their effects on synaptic transmission. For example, mutations in the KH-family member FMRP result in Fragile X Mental Retardation Syndrome, while mutations in the KH-family member QUAKING have been implicated in Schizophrenia. Two recent studies suggest that Sam68 is involved in the pathogenesis of Fragile X Tremor/Ataxia Syndrome, and Spinal Muscular Atrophy. Elucidation of Sam68's role in maintaining efficient synaptic transmission will provide valuable insights into how dysfunction of the family of KH-domain containing proteins, and Sam68 in particular, leads to neurological disease. Sam68 may serve dual roles at the synapse, first as a modulator of synaptic transmission through NMDA receptor trafficking, and second as a regulator of local protein synthesis at dendritic spines. This proposal includes training in a number of advanced laboratory skills in the fields of electrophysiology and molecular biology in order to conduct a detailed investigation of Sam68's role at the synapse. To study the effects of loss of Sam68 we will use in vivo molecular manipulations (e.g. viral injections), in addition to a complimentary set of experiments using a line of Sam68 null mice. We will examine the effect of loss of Sam68 on NMDA receptor trafficking using whole cell patch clamp recording and quantitative immunohistochemistry. We will examine the ability of Sam68 to regulate local protein synthesis at dendritic spines using fluorescence in situ hybridization, and the photoconvertable fluorescent protein Dendra2. Sam68 may represent a novel regulator of synaptic plasticity by participating in activity-dependent changes involving both receptor trafficking, and local protein synthesis.
PUBLIC HEALTH RELEVANCE: Neurological disorders may arise from inefficiencies in the mechanisms that ensure proper communication between neurons in the central nervous system. This project aims to understand the role of the RNA-binding protein Sam68 in ensuring proper neuronal transmission. Understanding this role will be helpful for guiding the development of therapies for neurological disorders resulting from dysfunction of Sam68 and related proteins.
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会议论文
Identifying neurobiological vulnerabilities in reward processing associated withsuicidal behavior in Veterans.
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批准号:10260719
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项目类别:
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资助金额:$0.0万
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财政年份:2022
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负责人:Matthew Klein
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依托单位:
The Role of Sam68 in Synaptic Transmission and Plasticity
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批准号:8389543
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项目类别:
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资助金额:$4.72万
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财政年份:2010
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负责人:Matthew Klein
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依托单位:
The Role of Sam68 in Synaptic Transmission and Plasticity
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批准号:8585939
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项目类别:
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资助金额:$1.53万
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财政年份:2010
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负责人:Matthew Klein
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依托单位:
The Role of Sam68 in Synaptic Transmission and Plasticity
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批准号:8213129
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项目类别:
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资助金额:$4.72万
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财政年份:2010
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负责人:Matthew Klein
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依托单位:
海外基金