Dissection of genetic pathways critical for myelinating Schwann cell development
Dissection of genetic pathways critical for myelinating Schwann cell development
批准号:
8081921
负责人:
Anthony Antonellis
金额:
$29.32万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-03-01 至 2016-02-29
关键词:
AddressAffectAnimal ModelAxonBinding ProteinsBinding SitesBoxingCandidate Disease GeneCell AdhesionCell physiologyCellsCellular biologyChickensCritical PathwaysDataDevelopmentDiseaseDissectionDistalEmbryoEnhancersEsthesiaGene ExpressionGene Expression RegulationGene ProteinsGene TargetingGeneral PopulationGenesGeneticGenomic SegmentGenomicsGoalsHandHomeostasisHumanIn VitroInheritedKnock-outKnowledgeLimb structureMotorMultiple SclerosisMusMuscle WeaknessMutateMutationPatientsPeripheral NervesPeripheral Nervous SystemPeripheral Nervous System DiseasesPhosphotransferasesPilot ProjectsPopulationProteinsPublic HealthRNAReporter GenesSH3 DomainsSchwann CellsSensorySequence AnalysisStagingStructureTestingTissuesVertebratesZebrafishadapter proteincell motilitycomparativefootgenome wide association studygenome-widehuman diseasein vivoinsightmalignant breast neoplasmmutantnoveltranscription factor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Peripheral neuropathies are a group of diseases characterized by impaired motor function and sensory loss in the extremities. Between 2-8% of the general population is affected with a peripheral neuropathy, making these diseases a significant public health concern. More than 80% of patients with inherited peripheral neuropathy carry mutations in genes encoding proteins critical for myelinating Schwann cells-a cell population that insulates and provides trophic factors to peripheral nerve axons. Currently, we have a very limited understanding of the transcriptional hierarchies involved in Schwann cell development and homeostasis. The SRY-box containing gene 10 (SOX10) encodes a transcription factor that is essential for Schwann cell development and function. Importantly, mutations in SOX10 and in loci regulated by SOX10 have been implicated in demyelinating peripheral neuropathies. Thus, the identification and characterization of novel SOX10 target loci will provide additional candidate genes for demyelinating peripheral neuropathies and key knowledge regarding Schwann cell biology. Toward this, we will: (1) Perform genome-wide identification of SOX10 target loci in myelinating Schwann cells; (2) Determine if SOX10 is necessary for the expression of two novel target genes (SH3KBP1 and BCAS3) in myelinating Schwann cells; and (3) Characterize the function of SH3KBP1 and BCAS3 in myelinating Schwann cells.
PUBLIC HEALTH RELEVANCE: Schwann cells are a critical component of peripheral nerves-structures essential for mobility and sensation in the hands and feet. Remarkably little is known about gene regulation in Schwann cells. The major goal of this proposal is to address this lack of knowledge through genome-wide identification of novel genes and proteins expressed in Schwann cells and determining how they contribute to Schwann cell function. These studies will provide key information on the function of peripheral nerves and associated human diseases such as peripheral neuropathy and multiple sclerosis.
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依托单位:
海外基金