The Role of CDO in Myogenic Differentiation
The Role of CDO in Myogenic Differentiation
批准号:
7429789
负责人:
Robert S. Krauss
金额:
$34.65万
依托单位国家:
美国
项目类别:
财政年份:
2000
资助国家:
美国
项目状态:
已结题
起止时间:
2000-04-01 至 2010-05-31
关键词:
ActinsAdhesivesBHLH ProteinBindingBiochemicalBiologicalBiological AssayCadherinsCalcineurinCell Adhesion MoleculesCell Differentiation processCell Surface ProteinsCell Surface ReceptorsCell surfaceCell-Adhesion Molecule ReceptorsCell-Cell AdhesionCellsComplexCytoskeletonE proteinEmbryonic DevelopmentEventFamilyFundingGene FusionGenerationsGenesGenetic TranscriptionGlycine decarboxylaseGoalsGuanosine Triphosphate PhosphohydrolasesHelix-Turn-Helix MotifsHeterodimerizationIn VitroLigandsLightLocalizedM-cadherinMediatingMicroscopyMitogen-Activated Protein KinasesModelingMolecularMultiprotein ComplexesMusMuscleMuscle DevelopmentMutagenesisMyoblastsMyopathyOrphanPathway interactionsProcessPropertyProteinsResearchRoleSignal PathwaySignal TransductionSignal Transduction PathwaySiteSkeletal MuscleSkeletal systemSomitesTissuesVertebratesbasecell typedevelopmental geneticsextracellularhuman MAPK14 proteinimprovedin vivomembermitogen-activated protein kinase p38myocyte-specific enhancer-binding factor 2myogenesisneogeninnetrin receptornetrin-3neurodevelopmentprotein functionreceptorresponserhotranscription factortranscription factor NF-AT c3
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Specification and differentiation of skeletal muscle precursors is controlled by the MyoD family of transcription factors, which cooperate with additional transcription factors to coordinate expression of muscle-specific genes and fusion into multinucleated myofibers. Several signaling pathways regulate the activity of these factors and promote myogenesis, but the cell surface proteins that initiate such pathways are not well understood. CDO is an orphan cell surface receptor expressed on muscle precursors. Mice lacking CDO display delayed skeletal muscle development, and CDO promotes myogenic differentiation in vitro. CDO functions as a component of a complex found at sites of cell-cell contact that contains several promyogenic proteins, including the closely related receptor, BOC; the cell adhesion molecules, N- and M-cadherin; and the netrin receptor, neogenin. CDO signals to activate MyoD via enhanced heterodimerization, likely by inducing hyperphosphorylation of its E protein partners, while cadherins and netrin/ neogenin signal to activate additional pathways. The components of this complex display interdependence in some of their activities (i.e., CDO requires cadherins, and BOC and neogenin require CDO). It is hypothesized that a multiprotein complex at sites of cell-cell contact permits diverse signaling events that regulate both morphological and transcriptional responses to be coordinated during differentiation. A multidisciplin- ary approach is proposed with the overall goal of gaining a mechanistic view of how CDO-containing complexes regulate skeletal muscle development. The Specific Aims are: 1) to identify the roles of the CDO binding partners, BOC and neogenin, in myogenesis in vivo; 2) to analyze biochemical and signaling properties of CDO-containing cell surface complexes; and 3) to analyze CDO-mediated hyperphosphorylation of E proteins. This research should shed light on fundamental processes by which skeletal muscles develop and therefore advance potential strategies for improved treatment of skeletal muscle diseases.
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项目类别:
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批准号:9107837
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资助金额:$41.63万
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财政年份:2015
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财政年份:2009
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依托单位:
Interactions between Shh pathway regulators and fetal alcohol exposure in mice
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批准号:8516408
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项目类别:
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资助金额:$35.3万
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财政年份:2009
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依托单位:
Interactions between Shh pathway regulators and fetal alcohol exposure in mice
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财政年份:2009
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依托单位:
Making Muscle in the Embryo and Adult
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资助金额:$2.5万
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财政年份:2009
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负责人:Robert S. Krauss
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依托单位:
Interactions between Shh pathway regulators and fetal alcohol exposure in mice
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项目类别:
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财政年份:2009
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依托单位:
Interactions between Shh pathway regulators and fetal alcohol exposure in mice
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资助金额:$37.95万
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财政年份:2009
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依托单位:
Gene-Environment Interaction in Holoprosencephaly: Role of Fetal Alcohol Exposure
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财政年份:2007
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Gene-Environment Interaction in Holoprosencephaly: Role of Fetal Alcohol Exposure
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Role of CD164 in Skeletal Myogenesis
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资助金额:$33.01万
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财政年份:2004
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依托单位:
The Role of CD164 in Skeletal Myogenesis
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批准号:6858637
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资助金额:$33.56万
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财政年份:2004
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依托单位:
The Role of CD164 in Skeletal Myogenesis
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财政年份:2004
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依托单位:
Role of CD164 in Skeletal Myogenesis
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资助金额:$31.82万
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财政年份:2004
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负责人:Robert S. Krauss
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依托单位:
Role of CD164 in Skeletal Myogenesis
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依托单位:
海外基金