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.
引用
收藏
页码:4577 / 4588
页数:12
相关论文
共 49 条
[1]   Phosphoinositide signaling pathways in nuclei are associated with nuclear speckles containing pre-mRNA processing factors [J].
Boronenkov, IV ;
Loijens, JC ;
Umeda, M ;
Anderson, RA .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (12) :3547-3560
[2]   Phosphatidylinositol(3)-phosphate signaling mediated by specific binding to RING FYVE domains [J].
Burd, CG ;
Emr, SD .
MOLECULAR CELL, 1998, 2 (01) :157-162
[3]   Phosphatidylinositol-3-OH kinases are Rab5 effectors [J].
Christoforidis, S ;
Miaczynska, M ;
Ashman, K ;
Wilm, M ;
Zhao, LY ;
Yip, SC ;
Waterfield, MD ;
Backer, JM ;
Zerial, M .
NATURE CELL BIOLOGY, 1999, 1 (04) :249-252
[4]   Phosphoinositides in membrane traffic [J].
Corvera, S ;
D'Arrigo, A ;
Stenmark, H .
CURRENT OPINION IN CELL BIOLOGY, 1999, 11 (04) :460-465
[5]   ISOLATION OF MONOCLONAL-ANTIBODIES SPECIFIC FOR HUMAN C-MYC PROTO-ONCOGENE PRODUCT [J].
EVAN, GI ;
LEWIS, GK ;
RAMSAY, G ;
BISHOP, JM .
MOLECULAR AND CELLULAR BIOLOGY, 1985, 5 (12) :3610-3616
[6]   Multivesicular body morphogenesis requires phosphatidylinositol 3-kinase activity [J].
Fernandez-Borja, M ;
Wubbolts, R ;
Calafat, J ;
Janssen, H ;
Divecha, N ;
Dusseljee, S ;
Neefjes, J .
CURRENT BIOLOGY, 1999, 9 (01) :55-58
[7]   Fab1p is essential for PtdIns(3)P 5-kinase activity and the maintenance of vacuolar size and membrane homeostasis [J].
Gary, JD ;
Wurmser, AE ;
Bonangelino, CJ ;
Weisman, LS ;
Emr, SD .
JOURNAL OF CELL BIOLOGY, 1998, 143 (01) :65-79
[8]   FYVE fingers bind Ptdins(3)P [J].
Gaullier, JM ;
Simonsen, A ;
D'Arrigo, A ;
Bremnes, B ;
Stenmark, H ;
Aasland, R .
NATURE, 1998, 394 (6692) :432-433
[9]   A QUANTITATIVE-ANALYSIS OF THE ENDOCYTIC PATHWAY IN BABY HAMSTER-KIDNEY CELLS [J].
GRIFFITHS, G ;
BACK, R ;
MARSH, M .
JOURNAL OF CELL BIOLOGY, 1989, 109 (06) :2703-2720
[10]   MEMBRANE-TRANSPORT IN THE ENDOCYTIC PATHWAY [J].
GRUENBERG, J ;
MAXFIELD, FR .
CURRENT OPINION IN CELL BIOLOGY, 1995, 7 (04) :552-563