Genetic Mechanisms of Axis Formation in Vertebrates
Genetic Mechanisms of Axis Formation in Vertebrates
批准号:
7884089
负责人:
ALEXANDER F SCHIER
金额:
$13.85万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-20 至 2010-08-31
关键词:
AddressBindingBiological ModelsCell PolarityCell TherapyCellsCongenital AbnormalityDefectDevelopmentDiseaseEmbryoEndodermEquilibriumEyeFundingGene Transfer TechniquesGenerationsGenesGeneticGerm LinesGoalsHumanImageIn VitroLeftLifeLinkMalignant NeoplasmsMediatingMesodermMicroRNAsMolecularMonitorMorphogenesisNodalOrganPlayProsencephalonReadingReagentRegenerative MedicineRegulationResearchRoleSignal PathwaySignal TransductionStem cellsStrabismusTechnologyTestingTimeTransforming Growth Factor betaTransgenic OrganismsVertebratesZebrafishcell fate specificationgastrulationin vivoinsightmorphogensmutantprogenitorresponsetranscription factor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The long-range goal of the proposed studies is to identify the mechanisms of cell fate specification and gastrulation during vertebrate development. Our focus is on the Nodal TGFbeta signaling pathway, which plays fundamental roles during gastrulation and left-right axis determination in vertebrates. In particular, Nodal signals are concentration-dependent inducers of mesodermal and endodermal progenitors and required for cell internalization during gastrulation. The proposed research addresses three fundamental questions: (A) How are Nodal signals interpreted in time and space? (B) How is Nodal signaling regulated? (C) Which genes mediate the effects of Nodal signaling during gastrulation? To address these questions, the following three aims are proposed. (1) To determine how Nodal signals are interpreted, the expression of Nodal signals will be modulated and the distribution of the Nodal effector Smad2 will be visualized in live embryos. This aim will test the hypothesis that cells constantly monitor Nodal signals and chose their fate according to both signal concentration and exposure time. (2) To determine the role of microRNAs in the regulation of Nodal signaling, microRNA function will be altered and the phenotypic consequences analyzed. This aim will test the hypothesis that microRNAs maintain Nodal signaling at equilibrium by dampening the expression of Nodal signaling components. (3) Nodal-regulated genes have been identified that are involved in the internalization and differentiation of mesodermal and endodermal progenitors. To determine the role of Nodal-regulated genes during gastrulation, in vivo imaging and mutant analysis will be combined. Abnormalities in Nodal signaling components in humans are associated with forebrain anomalies, left-right defects and cancer. The proposed studies should thus help to provide the necessary context for understanding human birth defects and disease. The in vitro generation of endoderm or mesoderm is crucial to develop cell-based therapies for regenerative medicine. The proposed studies will thus help to inform strategies to induce stem cells to differentiate into organ progenitors.
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Histone Modifications During Embryogenesis
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财政年份:2010
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Multicolor Fluorescent Analysis in Zebrafish
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批准号:7935634
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资助金额:$24.4万
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Generation of Hypocretin Neurons from Narcoleptic Patients
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财政年份:2010
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Multicolor Fluorescent Analysis in Zebrafish
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批准号:8142948
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项目类别:
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资助金额:$23.43万
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财政年份:2010
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Generation of Hypocretin Neurons from Narcoleptic Patients
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批准号:8066290
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资助金额:$24.7万
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财政年份:2010
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负责人:ALEXANDER F SCHIER
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依托单位:
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批准号:7743903
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项目类别:
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资助金额:$1.0万
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财政年份:2009
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负责人:ALEXANDER F SCHIER
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依托单位:
2009/2011 "Developmental Biology" Gordon Research Conferences
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批准号:7873006
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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:2009
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负责人:ALEXANDER F SCHIER
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依托单位:
2009/2011 "Developmental Biology" Gordon Research Conferences
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批准号:8079551
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项目类别:
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资助金额:$1.0万
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财政年份:2009
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Genetics of Sleep in Zebrafish
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批准号:8877616
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资助金额:$41.62万
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Genetics of Sleep in Zebrafish
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批准号:7628393
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资助金额:$33.58万
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依托单位:
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批准号:8692005
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依托单位:
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资助金额:$40.22万
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财政年份:2008
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负责人:ALEXANDER F SCHIER
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依托单位:
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资助金额:$42.25万
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财政年份:2008
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负责人:ALEXANDER F SCHIER
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依托单位:
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