Identification and characterization of a new oncogene derived from the regulatory subunit of phosphoinositide 3-kinase

被引:231
作者
Jimenez, C
Jones, DR
Rodríguez-Viciana, P
Gonzalez-García, A
Leonardo, E
Wennström, S
von Kobbe, C
Toran, JL
Borlado, LR
Calvo, V
Copin, SG
Albar, JP
Gaspar, ML
Diez, E
Marcos, MAR
Downward, J
Martinez, C
Mérida, I
Carrera, AC [1 ]
机构
[1] Univ Autonoma Madrid, Dept Immunol & Oncol, Ctr Nacl Biotecnol, E-28049 Madrid, Spain
[2] Imperial Canc Res Fund, London WC2A 3PX, England
[3] Univ Autonoma Madrid, Fac Med, CSIC, Inst Invest Biomed, E-28029 Madrid, Spain
[4] Univ Autonoma Madrid, CSIC, Ctr Mol Biol, E-28049 Madrid, Spain
[5] Inst Salud Carlos III, E-28220 Madrid, Spain
[6] SmithKline Beecham, E-28760 Madrid, Spain
关键词
mutants; phosphatidylinositol; 3-kinase; transformation;
D O I
10.1093/emboj/17.3.743
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
p85/p110 phosphoinositide 3-kinase (PI3K) is a heterodimer composed of a p85-regulatory and a p110-catalytic subunit, which is involved in a variety of cellular responses including cytoskeletal organization, cell survival and proliferation. We describe here the cloning and characterization of p65-PI3K, a mutant of the regulatory subunit of PI3K, which includes the initial 571 residues of the wild type p85 alpha-protein linked to a region conserved in the eph tyrosine kinase receptor family. We demonstrate that this mutation, obtained from a transformed cell, unlike previously engineered mutations of the regulatory subunit, induces the constitutive activation of PI3K and contributes to cellular transformation. This report links the PI3K enzyme to mammalian tumor development for the first time.
引用
收藏
页码:743 / 753
页数:11
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