The 145-kDa protein induced to associate with Shc by multiple cytokines is an inositol tetraphosphate and phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase

被引:563
作者
Damen, JE
Liu, L
Rosten, P
Humphries, RK
Jefferson, AB
Majerus, PW
Krystal, G
机构
[1] UNIV BRITISH COLUMBIA,TERRY FOX LAB,BRITISH COLUMBIA CANC RES CTR,VANCOUVER,BC V5Z 1L3,CANADA
[2] WASHINGTON UNIV,SCH MED,ST LOUIS,MO 63110
关键词
D O I
10.1073/pnas.93.4.1689
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A 145-kDa tyrosine-phosphorylated protein that becomes associated with She in response to multiple cytokines has been purified from the murine hemopoietic cell line B6SUtA(1). Amino acid sequence data were used to clone the cDNA encoding this protein from a B6SUtA(1) library. The predicted amino acid sequence encodes a unique protein containing an N-terminal src homology 2 domain, two consensus sequences that are targets for phosphotyrosine binding domains, a proline-rich region, and two motifs highly conserved among inositol polyphosphate 5-phosphatases. Cell lysates immunoprecipitated with antiserum to this protein exhibited both phosphatidylinositol 3,4,5-trisphosphate and inositol 1,3,4,5-tetrakisphosphate polyphosphate 5-phosphatase activity. This novel signal transduction intermediate may serve to modulate both Ras and inositol signaling pathways. Based on its properties, we suggest the 145-kDa protein be called SHIP for SH2-containing inositol phosphatase.
引用
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页码:1689 / 1693
页数:5
相关论文
共 47 条
[1]   PROLINE-RICH SEQUENCES THAT BIND TO SRC HOMOLOGY-3 DOMAINS WITH INDIVIDUAL SPECIFICITIES [J].
ALEXANDROPOULOS, K ;
CHENG, GH ;
BALTIMORE, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (08) :3110-3114
[2]   BINDING OF THE RAS ACTIVATOR SON OF SEVENLESS TO INSULIN-RECEPTOR SUBSTRATE-1 SIGNALING COMPLEXES [J].
BALTENSPERGER, K ;
KOZMA, LM ;
CHERNIACK, AD ;
KLARLUND, JK ;
CHAWLA, A ;
BANERJEE, U ;
CZECH, MP .
SCIENCE, 1993, 260 (5116) :1950-1952
[3]   RAPID FORMATION OF INOSITOL 1,3,4,5-TETRAKISPHOSPHATE FOLLOWING MUSCARINIC RECEPTOR STIMULATION OF RAT CEREBRAL CORTICAL SLICES [J].
BATTY, IR ;
NAHORSKI, SR ;
IRVINE, RF .
BIOCHEMICAL JOURNAL, 1985, 232 (01) :211-215
[4]  
BATZER AG, 1995, MOL CELL BIOL, V15, P4403
[5]   EPIDERMAL GROWTH-FACTOR REGULATES P21(RAS) THROUGH THE FORMATION OF A COMPLEX OF RECEPTOR, GRB2 ADAPTER PROTEIN, AND SOS NUCLEOTIDE EXCHANGE FACTOR [J].
BUDAY, L ;
DOWNWARD, J .
CELL, 1993, 73 (03) :611-620
[6]   PROTEIN-KINASE-B (C-AKT) IN PHOSPHATIDYLINOSITOL-3-OH INASE SIGNAL-TRANSDUCTION [J].
BURGERING, BMT ;
COFFER, PJ .
NATURE, 1995, 376 (6541) :599-602
[7]   NON-SH2 DOMAINS WITHIN INSULIN-RECEPTOR SUBSTRATE-1 AND SHC MEDIATE THEIR PHOSPHOTYROSINE-DEPENDENT INTERACTION WITH THE NPEY MOTIF OF THE INSULIN-LIKE GROWTH-FACTOR-I RECEPTOR [J].
CRAPARO, A ;
ONEILL, TJ ;
GUSTAFSON, TA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (26) :15639-15643
[8]   IDENTIFICATION OF A SPECIFIC INS(1,3,4,5)P-4-BINDING PROTEIN AS A MEMBER OF THE GAP1 FAMILY [J].
CULLEN, PJ ;
HSUAN, JJ ;
TRUONG, O ;
LETCHER, AJ ;
JACKSON, TR ;
DAWSON, AP ;
IRVINE, RF .
NATURE, 1995, 376 (6540) :527-530
[9]  
CUTLER RL, 1993, J BIOL CHEM, V268, P21463
[10]  
DAMEN JE, 1993, BLOOD, V81, P3204