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dc.contributor.advisorAnderson, Deborahen_US
dc.creatorChamberlain, Michael Deanen_US
dc.date.accessioned2007-06-27T14:54:42Zen_US
dc.date.accessioned2013-01-04T04:40:52Z
dc.date.available2007-06-28T08:00:00Zen_US
dc.date.available2013-01-04T04:40:52Z
dc.date.created2007-06en_US
dc.date.issued2007-06-28en_US
dc.date.submittedJune 2007en_US
dc.identifier.urihttp://hdl.handle.net/10388/etd-06272007-145442en_US
dc.description.abstractThe p85 subunit of phosphatidylinositol 3’-kinase (PI3K) has long been thought of as a regulatory subunit that has no other function than the regulation of the p110 catalytic subunit. Our laboratory is studying other roles of the p85 subunit, in particular determining the role of the p85 BH domain. The BH domain has homology to GTPase activating protein (GAP) domains that are involved in the stimulation of monomeric G proteins to hydrolyze their bound GTP to GDP. This converts the G protein from its active conformation to its inactive conformation. We have determined that p85 interacts with Rab proteins, monomeric G proteins that regulate vesicle fusion during the endocytosis of receptors. We have shown that p85 binds to Rab5 regardless of nucleotide-bound state of Rab5. The p85 subunit of PI3K has in vitro GAP activity towards Rab5. It was determined that p85 also has in vitro GAP activity towards Rab4, Rab7, Rab6 as well as the Rho-family G proteins, Rac1 and Cdc42. This GAP activity was localized to the BH domain of p85 and mutation of Arg 274 to Ala abolishes the GAP activity of p85. When this p85R274A mutant was expressed in cells, PDGFR degradation was severely inhibited and there was a corresponding increase in the duration of MAPK and Akt signalling. This increase in cell signalling caused a transformed phenotype in cells expressing the p85 protein with the Arg 274 mutation. These cells have lost contact inhibition for growth, are able to grow independent of attachment as well as in the presence of limited growth factors. They also form tumours in nude mice. These cellular effects seem to be due to an increase in receptor recycling because of the loss of the GAP activity of p85. This increase in receptor recycling may interfere with receptor targeting to the late endosome, which would cause the decrease in receptor degradation that is seen in the p85R274A cells.en_US
dc.language.isoen_USen_US
dc.subjectendocytosisen_US
dc.subjectPDGFRen_US
dc.subjectp85en_US
dc.subjectPI3Ken_US
dc.subjectRaben_US
dc.titleThe interaction of the p85 subunit of PI3K with rab proteinsen_US
thesis.degree.departmentBiochemistryen_US
thesis.degree.disciplineBiochemistryen_US
thesis.degree.grantorUniversity of Saskatchewanen_US
thesis.degree.levelDoctoralen_US
thesis.degree.nameDoctor of Philosophy (Ph.D.)en_US
dc.type.materialtexten_US
dc.type.genreThesisen_US
dc.contributor.committeeMemberSulakhe, Prakashen_US
dc.contributor.committeeMemberRoesler, William J.en_US
dc.contributor.committeeMemberLaferte, Suzanneen_US
dc.contributor.committeeMemberKhandelwal, Ramji L.en_US
dc.contributor.committeeMemberForsyth, George W.en_US


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