Identification of four novel human phosphoinositide 3-kinases defines a multi-isoform subfamily

被引:37
作者
Ho, LKF [1 ]
Liu, DX [1 ]
Rozycka, M [1 ]
Brown, RA [1 ]
Fry, MJ [1 ]
机构
[1] INST CANC RES,HADDOW LABS,SECT CELL BIOL & EXPT PATHOL,SIGNAL TRANSDUCT TEAM,SUTTON SM2 5NG,SURREY,ENGLAND
关键词
D O I
10.1006/bbrc.1997.6747
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) 3-kinases have critical roles in diverse cellular signalling processes and in protein trafficking. This suggests that like other intracellular signalling molecules, e.g., phospholipase C and protein kinase C, there might be a large family of PI 3-kinase isoforms with the individual members having discrete signalling roles. Reverse transcription-polymerase chain reaction methods, using degenerate oligonucleotide primers against the lipid kinase consensus region, revealed eight sequences from human cDNA containing a high degree of identity to the family of PI 3-kinases. The sequences obtained included the previously described p110 alpha, p110 beta, and p110 gamma isoforms and HsVps34. Additionally, we have identified four novel sequences which are related to PI 3-kinases. Three of the novel sequences would appear to form a distinct sub-family of PI 3-kinases. We report the expression of these novel PI 3-kinases in human tissues and in cells derived from normal breast. (C) 1997 Academic Press.
引用
收藏
页码:130 / 137
页数:8
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