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REGULATION OF BETA-CATENIN NUCLEARIZATION

REGULATION OF BETA-CATENIN NUCLEARIZATION
β-连环蛋白核化的调控
批准号:
6573267
负责人:
CHARLES A. ETTENSOHN
金额:
$24.56万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-03-01 至 2007-02-28

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英文摘要
DESCRIPTION (provided by applicant): The accumulation of beta-catenin in the nuclei of specific blastomeres is a critical early step in animal development. In all deuterostomes (echinoderms and chordates/vertebrates) that have been studied, accumulation of beta-catenin in the nuclei of specific blastomeres along the axis of the cleavage stage embryo is one of the first indications of embryonic polarity. This differential "nuclearization" of beta-catenin is essential for proper germ layer formation and the establishment of inductive centers. The sea urchin embryo is a powerful model system for studying beta-catenin nuclearization. The embryo develops externally and is optically transparent, facilitating the application of a wide variety of light optical technologies. The system is unique in that specific cell types can be isolated from early embryos in large quantities. Most of the molecules of the beta-catenin pathway have been cloned from sea urchin and a large number of molecular biological tools are available. Gene expression can be manipulated by expression of dominant negative constructs and by microinjection of "morpholino" antisense oligonucleotides. The proposed work will identify the mechanisms that underlie beta-catenin nuclearization in early embryos. There are two major aims: 1) Using GFP-tagged proteins and time-lapse, 3-D confocal microscopy, the dynamics and turnover of key regulators of beta-catenin degradation will be studied in vivo. We will measure the half-life of beta-catenin in specific blastomeres of the early embryo, which will provide essential information concerning the cellular and molecular mechanisms of differential nuclearization. Through blastomere isolation experiments, we will test the role of cell-cell interactions in regulating beta-catenin nuclearization. 2) We will test three major models of GSK3 regulation along the embryo axis. In addition, using dominant negative constructs and morpholinos, we will examine the developmental function of two regulators of GSK3 activity, disheveled and Akt/PKB.
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Enhanced Echinobase: A Community Genomics Research Resource For The Future
  • 批准号:
    10715578
  • 项目类别:
  • 资助金额:
    $78.69万
  • 财政年份:
    2023
  • 负责人:
    CHARLES A. ETTENSOHN
  • 依托单位:
Mining Information from Echinoderm Genomes and the Scientific Literature
  • 批准号:
    10715580
  • 项目类别:
  • 资助金额:
    $14.94万
  • 财政年份:
    2023
  • 负责人:
    CHARLES A. ETTENSOHN
  • 依托单位:
Mining the Scientific Literature and Building a Pan-Echinoderm Gene Expression Database
  • 批准号:
    10241292
  • 项目类别:
  • 资助金额:
    $12.05万
  • 财政年份:
    2018
  • 负责人:
    CHARLES A. ETTENSOHN
  • 依托单位:
Enhanced Echinobase: A Community Genome Resource for the Future
  • 批准号:
    10241290
  • 项目类别:
  • 资助金额:
    $52.49万
  • 财政年份:
    2018
  • 负责人:
    CHARLES A. ETTENSOHN
  • 依托单位:
国内基金
海外基金
增生性玻璃体视网膜病变早期钙黏蛋白(Cadherins)异常表达启动视网膜色素上皮细胞游离的分子机制
  • 批准号:
    81770939
  • 项目类别:
    面上项目
  • 资助金额:
    56.0万元
  • 批准年份:
    2017
  • 负责人:
    王方
  • 依托单位:
Beta-catenin/Cadherins, EphBs 在平衡颅神经嵴细胞的粘附和迁徙机制的研究
  • 批准号:
    81400494
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    23.0万元
  • 批准年份:
    2014
  • 负责人:
    刘人恺
  • 依托单位:
Cadherins与nectins在青少年期慢性社会应激损害小鼠前额叶形态可塑性与功能中的作用
  • 批准号:
    81401129
  • 项目类别:
    青年科学基金项目
  • 资助金额:
    23.0万元
  • 批准年份:
    2014
  • 负责人:
    李继涛
  • 依托单位: