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Localization of phosphatidylinositol 3-phosphate in yeast and mammalian cells
被引:863
作者:
Gillooly, DJ
Morrow, IC
Lindsay, M
Gould, R
Bryant, NJ
Gaullier, JM
Parton, RG
[1
]
Stenmark, H
机构:
[1] Norwegian Radium Hosp, Dept Biochem, Inst Canc Res, N-0310 Oslo, Norway
[2] Univ Queensland, Ctr Cellular & Mol Biol, St Lucia, Qld 4072, Australia
[3] Univ Queensland, Ctr Microscopy & Microanal, St Lucia, Qld 4072, Australia
[4] Univ Queensland, Dept Physiol & Pharmacol, St Lucia, Qld 4072, Australia
关键词:
electron microscopy;
membrane traffic;
multivesicular body;
phosphoinositide;
PI;
3-kinase;
D O I:
10.1093/emboj/19.17.4577
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Phosphatidylinositol 3-kinase (PI3K) regulates several vital cellular processes, including signal transduction and membrane trafficking. In order to study the intracellular localization of the PI3K product, phosphatidylinositol 3-phosphate [PI(3)P], we constructed a probe consisting of two PI(3)P-binding FYVE domains, The probe was found to bind specifically, and with high affinity, to PI(3)P both in vitro and in vivo. When expressed in fibroblasts, a tagged probe localized to endosomes, as detected by fluorescence microscopy, Electron microscopy of untransfected fibroblasts showed that PI(3)P is highly enriched on early endosomes and in the internal vesicles of multivesicular endosomes, While yeast cells deficient in PI3K activity (vps15 and vps34 mutants) were not labelled, PI(3)P was found on intralumenal vesicles of endosomes and vacuoles of wild-type yeast. vps27 Delta yeast cells, which have impaired endosome to vacuole trafficking, showed a decreased vacuolar labelling and increased endosome labelling, Thus PI(3)P follows a conserved intralumenal degradation pathway, and its generation, accessibility and turnover are likely to play a crucial role in defining the early endosome and the subsequent steps leading to multivesicular endosome formation.
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页码:4577 / 4588
页数:12
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