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
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