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Novel role of an aquaporin in endosome biogenesis and Notch signaling

Novel role of an aquaporin in endosome biogenesis and Notch signaling
水通道蛋白在内体生物发生和Notch信号传导中的新作用
批准号:
7733327
负责人:
Mark E Fortini
金额:
$47.13万
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至

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中文摘要
翻译
Notch信号传导需要受体及其配体的内吞作用, 内部化Notch的路由对于信号传输和再循环都有影响 和未激活受体的降解。我们发现一种典型的果蝇 一种称为大脑(bib)的突变体在Notch的内体积累方面表现出明显的缺陷 和其他表面衍生的蛋白质。Bib蛋白具有N-末端结构域, 与哺乳动物水通道蛋白高度同源,其转运水、离子和其它小分子物质, 溶质穿过生物膜。利用细胞生物学和遗传学方法,我们有 确定Bib对于早期内体的成熟和适当的膜是必不可少的 Notch在内体途径中的运输。在没有Bib功能的情况下,内体是 主要是在早期内陷阶段和形成酸化溶酶体 细胞器受损。这些影响伴随着异常的亚细胞运输, 分泌酶切割产生的细胞内Notch片段,强调γ Notch膜运输对于有效信号转导的重要性。这个项目 揭示了水通道蛋白家族成员在细胞器生物发生中的一种新功能, 内体-溶酶体运输途径,我们的初步研究最近发表在 Cell(Kanwar and Fortini,2008).我们未来的计划包括搜索围嘴互动 蛋白质,以及对Bib与其他内体运输关系的更详细研究 因素
英文摘要
Notch signaling requires endocytosis of both the receptor and its ligand, and endosomal routing of internalized Notch has implications for signal transmission as well as recycling and degradation of unactivated receptors. We have discovered that a classical Drosophila mutant termed big brain (bib) exhibits striking defects in the endosomal accumulation of Notch and other surface-derived proteins. The Bib protein possesses an N-terminal domain that is highly homologous to mammalian aquaporins, which transport water, ions, and other small solutes across biological membranes. Using cell biological and genetic approaches, we have determined that Bib is essential for the maturation of early endosomes and the proper membrane trafficking of Notch in the endosomal pathway. In the absence of Bib function, endosomes are arrested primarily at an early invaginating stage and the formation of acidified lysosomal organelles is impaired. These effects are accompanied by aberrant subcellular trafficking of the intracellular Notch fragment produced by γ-secretase cleavage, emphasizing the importance of Notch membrane trafficking for efficient signal transduction. This project has uncovered a novel function for an aquaporin family member in organelle biogenesis within the endosome-lysosome trafficking route, and our initial studies were published recently in Cell (Kanwar and Fortini, 2008). Our future plans include searches for Bib-interacting proteins, and more detailed studies on the relationship of Bib to other endosomal trafficking factors.
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Trafficking and Proteolysis of Notch and Other Gamma-Secretase Substrates
  • 批准号:
    8067753
  • 项目类别:
  • 资助金额:
    $31.42万
  • 财政年份:
    2009
  • 负责人:
    Mark E Fortini
  • 依托单位:
Trafficking and Proteolysis of Notch and Other Gamma-Secretase Substrates
  • 批准号:
    8259436
  • 项目类别:
  • 资助金额:
    $31.42万
  • 财政年份:
    2009
  • 负责人:
    Mark E Fortini
  • 依托单位:
Trafficking and Proteolysis of Notch and Other Gamma-Secretase Substrates
  • 批准号:
    7808761
  • 项目类别:
  • 资助金额:
    $31.74万
  • 财政年份:
    2009
  • 负责人:
    Mark E Fortini
  • 依托单位:
ALZHEIMER'S DISEASE RELATED PRESENILINS
  • 批准号:
    6133535
  • 项目类别:
  • 资助金额:
    $4.03万
  • 财政年份:
    2000
  • 负责人:
    Mark E Fortini
  • 依托单位:
海外基金