Chemical Regulation of Zebrafish Gene Expression
Chemical Regulation of Zebrafish Gene Expression
批准号:
7459381
负责人:
JAMES K CHEN
金额:
$8.33万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-07-01 至 2010-06-30
关键词:
AdultAgonistAreaBehaviorBiological ModelsBiological ProcessBiomedical ResearchCellsChemicalsCommunitiesComplexDevelopmentDiseaseDisruptionEmbryoEpitopesEvaluationGene ExpressionGene Expression RegulationGenerationsGenesGeneticGenetic ProgrammingGoalsGrowthHuman DevelopmentLaboratoriesLightMembraneMetabolismMethodsMicroinjectionsModelingMolecularOrganismPatternPersonal SatisfactionPhysiologicalPhysiologyPositioning AttributeReagentRegulationReporterResearchResearch PersonnelRoleSignal TransductionStagingSynthesis ChemistrySystemTailTechniquesTestingTranscriptional ActivationTransgenic OrganismsVertebrate BiologyZebrafishbaseblastomere structurechemical synthesisdaydesignecdysone receptorgene functionhomologous recombinationimprovedin vivointerestnotochordpositional cloningprogramssmoothened signaling pathwaysomitogenesistechnology developmenttooltranscription factortumorigenesis
中文摘要
虽然斑马鱼已经成为脊椎动物生物学的理想模型,但用于评估斑马鱼的方法仍然存在不足。
斑马鱼的基因功能仍然不发达。这个应用程序描述了两个跨学科的战略
用于通过化学试剂在时间和空间上控制斑马鱼中的基因表达。一种方法
建立在斑马鱼群体使用吗啉代低聚物选择性抑制基因表达的基础上
并且涉及笼状吗啉代的合成,所述笼状吗啉代在被光激活时变得发荧光。的
另一种方法使用蜕皮激素受体激动剂诱导转录激活,
提供额外空间控制的激动剂。这两种策略都将产生具有定制基因的斑马鱼
表达模式,为在分子水平上理解脊椎动物生理学提供了新的机会。
系统层面。由于斑马鱼被用于研究脊椎动物生物学的多个方面,这些新的
实验能力将促进我们对人类发育、生理和疾病的理解。
英文摘要
Although the zebrafish has emerged as an ideal model of vertebrate biology, methods for evaluating
zebrafish gene function remain underdeveloped. This application describes two interdisciplinary strategies
for temporally and spatially controlling gene expression in zebrafish through chemical reagents. One method
builds upon the zebrafish community's use of morpholino oligomers to selectively inhibit gene expression
and involves the synthesis of caged morpholinos that become fluorescent upon their activation by light. The
other approach uses ecdysone receptor agonists to induce transcriptional activation, with photoactivatable
agonists providing additional spatial control. Both strategies will generate zebrafish with tailored gene
expression patterns, providing new opportunities for understanding vertebrate physiology at the molecular
and systems levels. Since zebrafish are used to study multiple aspects of vertebrate biology, these new
experimental capabilities will advance our understanding of human development, physiology, and disease.
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资助金额:$41.76万
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资助金额:$87.07万
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财政年份:2019
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依托单位:
Chemical tools for developmental biology
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财政年份:2018
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Chemical tools for developmental biology
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财政年份:2018
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Gli1-selective inhibitors of the Hedgehog signaling pathway
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财政年份:2015
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负责人:JAMES K CHEN
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依托单位:
Development of lariat-shaped caged morpholinos for optochemical gene regulation
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资助金额:$44.0万
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财政年份:2014
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负责人:JAMES K CHEN
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依托单位:
Chemical genetic dissection of Hipk4-dependent Hedgehog pathway activation
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资助金额:$19.63万
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财政年份:2014
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负责人:JAMES K CHEN
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依托单位:
Chemical genetic dissection of Hipk4-dependent Hedgehog pathway activation
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批准号:8611320
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项目类别:
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资助金额:$24.14万
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财政年份:2014
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负责人:JAMES K CHEN
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依托单位:
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批准号:9110285
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项目类别:
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资助金额:$42.48万
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财政年份:2014
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负责人:JAMES K CHEN
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依托单位:
A high-throughput screen for small-molecule antagonists of Gli function
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项目类别:
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资助金额:$3.95万
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财政年份:2011
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依托单位:
A high-throughput screen for small-molecule antagonists of Gli function
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财政年份:2011
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依托单位:
Deciphering T-box gene-dependent mesoderm development with synthetic probes
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负责人:JAMES K CHEN
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依托单位:
Deciphering T-box gene-dependent mesoderm development with synthetic probes
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项目类别:
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资助金额:$33.16万
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财政年份:2010
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依托单位:
Deciphering T-box gene-dependent mesoderm development with synthetic probes
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依托单位:
国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
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负责人:乔安娜
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依托单位: