Regulation of TCF3 by Wnt signaling
Wnt 信号传导对 TCF3 的调节
基本信息
- 批准号:8238333
- 负责人:
- 金额:$ 41.41万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2011
- 资助国家:美国
- 起止时间:2011-04-01 至 2015-03-31
- 项目状态:已结题
- 来源:
- 关键词:AdultAttentionBiochemicalBiologicalBiological AssayCell DeathCell Differentiation processCell ProliferationCell Proliferation RegulationCellsColon CarcinomaComplexCutaneous MelanomaDNADetermination of DeathDevelopmentDiseaseEctoderm CellEmbryoEmbryonic DevelopmentFamilyGene ActivationGene ExpressionGene Expression RegulationGene TargetingGeneticGenetic TranscriptionGoalsHomeostasisHumanKnowledgeLeadLigandsMalignant NeoplasmsMammalian CellMediatingModificationMolecularPathway interactionsPatternPhosphorylationPlayPost-Translational Protein ProcessingPreclinical Drug EvaluationProtein KinaseProteinsRegulationResearchRoleSignal PathwaySignal TransductionSiteSkin NeoplasmsTCF Transcription FactorTCF3 geneTestingTherapeuticTissuesTranscription Repressor/CorepressorVertebratesWnt proteinsXenopusbaseblastomere structurecell behaviorcell fate specificationcofactoreggexpression cloninggene repressionhomeodomainloss of functionmembermutantnoveloverexpressionpublic health relevancereceptorresearch studyresponsetumortumorigenesis
项目摘要
DESCRIPTION (provided by applicant): The T-cell factor (TCF) family plays key roles in the control of gene expression in response to secreted Wnt proteins. Wnt pathways operate to modulate cell proliferation, migratory behavior, cell fate determination and cell death. This proposal aims to study the regulation of TCF3, a transcriptional repressor which has been implicated in Wnt signaling during cell differentiation and tumorigenesis. Our preliminary experiments in Xenopus ectoderm and mammalian cells identified a specific post-translational change in TCF3 protein mobility that correlates with Wnt target gene activation. This effect has been demonstrated to involve homeodomain-interacting protein kinase (HIPK), leading to a hypothesis that Wnt proteins act via HIPK2 and TCF3 to regulate their transcriptional targets. This hypothesis will be tested in mammalian cells and Xenopus eggs, in which biochemical and cell biological approaches can be combined with rapid functional analysis of underlying mechanisms. To investigate roles of TCF3 postranslational modification for Wnt-dependent activation of target genes, non- phosphorylatable and phosphomimetic TCF3 mutant proteins will be compared in morphological and molecular assays. Other experiments will elucidate how Wnt signals activate HIPK and trigger TCF3 post-translational modifications that are critical for target gene regulation. These studies will help characterize basic signaling networks normally leading to cell proliferation and differentiation, but which are misregulated during disease. Given the association of Wnt pathways with cancer, the knowledge of how TCF3 is regulated will serve as a basis for new drug screens and should lead to the development of crucial therapeutic strategies.
PUBLIC HEALTH RELEVANCE: This application concerns the function of TCF3, a Wnt-dependent transcriptional repressor that is essential for the regulation of cell proliferation. Since Wnt pathways have been found activated in a variety of tumors, the proposed studies are highly relevant to human cancer.
描述(由申请人提供):T细胞因子(TCF)家族在控制分泌的Wnt蛋白的基因表达方面发挥关键作用。WNT通路调节细胞增殖、迁移行为、决定细胞命运和细胞死亡。这项建议旨在研究转录抑制因子TCF3的调控,该转录抑制因子参与了细胞分化和肿瘤发生过程中的Wnt信号。我们在非洲爪哇外胚层和哺乳动物细胞中的初步实验发现,TCF3蛋白迁移率在翻译后发生了特定的变化,与Wnt靶基因的激活相关。这一效应已被证明涉及同源结构域相互作用蛋白激酶(HIPK),导致了一种假设,即Wnt蛋白通过HIPK2和TCF3调节其转录靶标。这一假设将在哺乳动物细胞和非洲爪哇卵中进行测试,在这些细胞中,生化和细胞生物学方法可以与潜在机制的快速功能分析相结合。为了研究TCF3翻译后修饰在Wnt依赖的靶基因激活中的作用,我们将从形态和分子水平上比较非磷酸化和拟磷酸化的TCF3突变蛋白。其他实验将阐明Wnt信号如何激活HIPK并触发TCF3翻译后修饰,这对靶基因调控至关重要。这些研究将有助于确定通常导致细胞增殖和分化的基本信号网络的特征,但这些网络在疾病期间被错误地调控。鉴于Wnt通路与癌症的关联,了解TCF3是如何被调控的将成为新药筛选的基础,并应导致关键治疗策略的开发。
公共卫生相关性:这项应用涉及TCF3的功能,TCF3是一种依赖Wnt的转录抑制因子,对调节细胞增殖至关重要。由于已发现Wnt通路在多种肿瘤中被激活,因此拟议的研究与人类癌症高度相关。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Sergei Sokol其他文献
Sergei Sokol的其他文献
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{{ truncateString('Sergei Sokol', 18)}}的其他基金
Extracellular regulation of Xenopus development
非洲爪蟾发育的细胞外调节
- 批准号:
10462530 - 财政年份:2018
- 资助金额:
$ 41.41万 - 项目类别:
Extracellular regulation of Xenopus development
非洲爪蟾发育的细胞外调节
- 批准号:
10237948 - 财政年份:2018
- 资助金额:
$ 41.41万 - 项目类别:
Cell polarity and morphogenesis in Xenopus embryos
爪蟾胚胎的细胞极性和形态发生
- 批准号:
10673928 - 财政年份:2017
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$ 41.41万 - 项目类别:
Cell polarity and morphogenesis in Xenopus embryos
爪蟾胚胎的细胞极性和形态发生
- 批准号:
10406539 - 财政年份:2017
- 资助金额:
$ 41.41万 - 项目类别:
Cell polarity and morphogenesis in Xenopus embryos
爪蟾胚胎的细胞极性和形态发生
- 批准号:
10795267 - 财政年份:2017
- 资助金额:
$ 41.41万 - 项目类别:
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