Cloning and Characterization of a G Protein-Activated Human Phosphoinositide-3 Kinase

Borislav Stoyanov(Max Planck Institute for the Science of Human History), Stefano Volinia(Ludwig Cancer Research), Theodor Hanck(Max Planck Institute for the Science of Human History), Ignacio Rubio(Max Planck Institute for the Science of Human History), Michael Loubtchenkov(Max Planck Institute for the Science of Human History), Daria Malek(Universität Ulm), Stefka Stoyanova(Jena University Hospital), Bart Vanhaesebroeck(Ludwig Cancer Research), Ritu Dhand(Ludwig Cancer Research), Bernd Nürnberg(Freie Universität Berlin), Peter Gierschik(Universität Ulm), Klaus Seedorf(Max Planck Institute of Biochemistry), J. Justin Hsuan(Ludwig Cancer Research), Michael D. Waterfield(Ludwig Cancer Research), Reinhard Wetzker(Max Planck Institute for the Science of Human History)
Science
August 4, 1995
Cited by 675

Abstract

Phosphoinositide-3 kinase activity is implicated in diverse cellular responses triggered by mammalian cell surface receptors and in the regulation of protein sorting in yeast. Receptors with intrinsic and associated tyrosine kinase activity recruit heterodimeric phosphoinositide-3 kinases that consist of p110 catalytic subunits and p85 adaptor molecules containing Src homology 2 (SH2) domains. A phosphoinositide-3 kinase isotype, p110 gamma, was cloned and characterized. The p110 gamma enzyme was activated in vitro by both the alpha and beta gamma subunits of heterotrimeric guanosine triphosphate (GTP)-binding proteins (G proteins) and did not interact with p85. A potential pleckstrin homology domain is located near its amino terminus. The p110 gamma isotype may link signaling through G protein-coupled receptors to the generation of phosphoinositide second messengers phosphorylated in the D-3 position.


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