Evidence that a phosphatidylinositol 3,4,5-trisphosphate-binding protein can function in nucleus

被引:117
作者
Tanaka, K
Horiguchi, K
Yoshida, T
Takeda, M
Fujisawa, H
Takeuchi, K
Umeda, M
Kato, S
Ihara, S
Nagata, S
Fukui, Y
机构
[1] Univ Tokyo, Grad Sch Agr & Life Sci, Dept Appl Biol Chem, Biol Chem Lab,Bunkyo Ku, Tokyo 1130032, Japan
[2] Inst Environm Toxicol, Div Toxicol, Mitsukaido, Ibaraki 3030043, Japan
[3] Tokyo Metropolitan Inst Med Sci, Dept Inflammat Res, Bunkyo Ku, Tokyo 1138613, Japan
[4] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
关键词
D O I
10.1074/jbc.274.7.3919
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
PIP3BP is a phosphatidylinositol 3,4,5-trisphosphate-binding protein (PIP3BP) abundant in brain, containing a zinc: finger motif and two pleckstrin homology (PH) domains. Staining of rat brain cells with anti-PIP3BP antibody and determination of localization of PIP3BP fused to the green fluorescent protein (GFP-PIP3BP) revealed that PIP3BP was targeted to the nucleus. Targeting was dependent on a putative nuclear localization signal in PIP3BP. Generation of PIP3 in the nucleus was detected in H2O2-treated 293T cells, nerve growth factor (NGF)-treated PC12 cells, and platelet-derived growth factor (PDGF)-treated NIH 3T3 cells. Translocation of phosphatidylinositol 3-kinase (PI 3-kinase) to the nucleus and enhanced activity of PI 3-kinase in the nucleus fraction were observed after H2O2 treatment of 293T cells, suggesting that PI 3-kinase can be activated in the nucleus as well as in the membrane after appropriate stimulation of the cells, Go-expression of the constitutively active PI 3-kinase with PIP3BP resulted in exportation of the protein from the nucleus to the cytoplasm, suggesting that PIP3BP can function as a PIP3-binding protein in the intact cells. These results imply that there may be an unknown function of PI 3-kinase in the nucleus.
引用
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页码:3919 / 3922
页数:4
相关论文
共 30 条
[1]   EGF or PDGF receptors activate atypical PKC lambda through phosphatidylinositol 3-kinase [J].
Akimoto, K ;
Takahashi, R ;
Moriya, S ;
Nishioka, N ;
Takayanagi, J ;
Kimura, K ;
Fukui, Y ;
Osada, S ;
Mizuno, K ;
Hirai, S ;
Kazlauskas, A ;
Ohno, S .
EMBO JOURNAL, 1996, 15 (04) :788-798
[2]   Characterization of a 3-phosphoinositide-dependent protein kinase which phosphorylates and activates protein kinase B alpha [J].
Alessi, DR ;
James, SR ;
Downes, CP ;
Holmes, AB ;
Gaffney, PRJ ;
Reese, CB ;
Cohen, P .
CURRENT BIOLOGY, 1997, 7 (04) :261-269
[3]   PDGF-DEPENDENT TYROSINE PHOSPHORYLATION STIMULATES PRODUCTION OF NOVEL POLYPHOSPHOINOSITIDES IN INTACT-CELLS [J].
AUGER, KR ;
SERUNIAN, LA ;
SOLTOFF, SP ;
LIBBY, P ;
CANTLEY, LC .
CELL, 1989, 57 (01) :167-175
[4]  
CARPENTER CL, 1990, J BIOL CHEM, V265, P19704
[5]  
FUKUI Y, 1991, ONCOGENE, V6, P407
[6]  
Fukui Y, 1998, J BIOCHEM-TOKYO, V124, P1
[7]   ESTABLISHMENT OF A NORADRENERGIC CLONAL LINE OF RAT ADRENAL PHEOCHROMOCYTOMA CELLS WHICH RESPOND TO NERVE GROWTH-FACTOR [J].
GREENE, LA ;
TISCHLER, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (07) :2424-2428
[8]   Identification and cloning of centaurin-alpha - A novel phosphatidylinositol 3,4,5-trisphosphate-binding protein from rat brain [J].
HammondsOdie, LP ;
Jackson, TR ;
Profit, AA ;
Blader, IJ ;
Turck, CW ;
Prestwich, GD ;
Theibert, AB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (31) :18859-18868
[9]   Role of substrates and products of PI3-kinase in regulating activation of Rac-related guanosine triphosphatases by Vav [J].
Han, JW ;
Luby-Phelps, K ;
Das, B ;
Shu, XD ;
Xia, Y ;
Mosteller, RD ;
Krishna, UM ;
Falck, JR ;
White, MA ;
Broek, D .
SCIENCE, 1998, 279 (5350) :558-560
[10]  
HAYASHI H, 1993, J BIOL CHEM, V268, P7107