Identification and cDNA cloning of a novel mammalian C2 domain-containing phosphoinositide 3-kinase, HsC2-PI3K

被引:58
作者
Brown, RA
Ho, LKF
WeberHall, SJ
Shipley, JM
Fry, MJ
机构
[1] INST CANC RES,SECT CELL BIOL & EXPT PATHOL,SIGNAL TRANSDUCT TEAM,HADDOW LABS,SUTTON SM2 5NG,SURREY,ENGLAND
[2] INST CANC RES,SECT CELL BIOL & EXPT PATHOL,MOL CYTOGENET TEAM,HADDOW LABS,SUTTON SM2 5NG,SURREY,ENGLAND
关键词
D O I
10.1006/bbrc.1997.6495
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
Phosphoinositide (PI) S-kinases have been shown to have critical roles in signal transduction, cell transformation and intracellular protein trafficking. Reverse-transcription polymerase chain reaction methods, using degenerate primers derived from the lipid kinase consensus region, were utilised to identify PI S-kinases in the normal human breast. Here we report the cDNA cloning of a novel human PI 3-kinase isoform, HsC2-PI3K. This PI 3-kinase is most closely related to the recently described C2 domain-containing family of PI 3-kinases which includes Drosophila PI3K_68D/cpk and murine cpk-m/p170. Sequence analysis suggests that HsC2-PI3K is a second distinct mammalian member of the C2 domain-containing PI 3-kinase family. Northern blot analysis of human tissues indicates that HsC2-PI3K is widely expressed. Fluorescence in situ hybridisation has mapped HsC2-PI3K to chromosome 1q32. (C) 1997 Academic Press.
引用
收藏
页码:537 / 544
页数:8
相关论文
共 48 条
[1]   WORTMANNIN IS A POTENT PHOSPHATIDYLINOSITOL 3-KINASE INHIBITOR - THE ROLE OF PHOSPHATIDYLINOSITOL 3,4,5-TRISPHOSPHATE IN NEUTROPHIL RESPONSES [J].
ARCARO, A ;
WYMANN, MP .
BIOCHEMICAL JOURNAL, 1993, 296 :297-301
[2]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159
[3]  
CLARKE C, 1993, EPITHELIAL CELL BIOL, V3, P38
[4]   The 145-kDa protein induced to associate with Shc by multiple cytokines is an inositol tetraphosphate and phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase [J].
Damen, JE ;
Liu, L ;
Rosten, P ;
Humphries, RK ;
Jefferson, AB ;
Majerus, PW ;
Krystal, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (04) :1689-1693
[5]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[6]   Cloning and expression of a human placenta inositol 1,3,4,5-tetrakisphosphate and phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase [J].
Drayer, AL ;
Pesesse, X ;
DeSmedt, F ;
Woscholski, R ;
Parker, P ;
Erneux, C .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 225 (01) :243-249
[7]   Direct regulation of the Akt proto-oncogene product by phosphatidylinositol-3,4-bisphosphate [J].
Franke, TF ;
Kaplan, DR ;
Cantley, LC ;
Toker, A .
SCIENCE, 1997, 275 (5300) :665-668
[8]   PURIFICATION AND CHARACTERIZATION OF A PHOSPHATIDYLINOSITOL 3-KINASE COMPLEX FROM BOVINE BRAIN BY USING PHOSPHOPEPTIDE AFFINITY COLUMNS [J].
FRY, MJ ;
PANAYOTOU, G ;
DHAND, R ;
RUIZLARREA, F ;
GOUT, I ;
NGUYEN, O ;
COURTNEIDGE, SA ;
WATERFIELD, MD .
BIOCHEMICAL JOURNAL, 1992, 288 :383-393
[9]   STRUCTURE, REGULATION AND FUNCTION OF PHOSPHOINOSITIDE 3-KINASES [J].
FRY, MJ .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1994, 1226 (03) :237-268
[10]   PLATELET-DERIVED GROWTH-FACTOR STIMULATES SYNTHESIS OF PTDLNS(3,4,5)P3 BY ACTIVATING A PTDLNS(4,5)P2 3-OH KINASE [J].
HAWKINS, PT ;
JACKSON, TR ;
STEPHENS, LR .
NATURE, 1992, 358 (6382) :157-159