Journal
CELLULAR SIGNALLING
Volume 22, Issue 11, Pages 1700-1707Publisher
ELSEVIER SCIENCE INC
DOI: 10.1016/j.cellsig.2010.06.010
Keywords
GAIP; MAPK; Ras; RGS19
Categories
Funding
- Hong Kong RGC [HKUST1/06C, HKUST6443/06M]
- UGC [AoE/B-15/01]
- Hong Kong Jockey Club
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Regulator of G protein signaling 19 (RGS19), also known as G alpha-interacting protein (GAIP), is a GTPase activating protein (GAP) for G(alpha)i subunits. Apart from its GAP function, RGS19 has been implicated in growth factor signaling through binding to GAIP-interacting protein C-terminus (GIPC) via its C-terminal PDZ-binding motif. To gain additional insight on its function, we have stably expressed RGS19 in a number of mammalian cell lines and examined its effect on cell proliferation. Interestingly, overexpression of RGS19 stimulated the growth of HEK293, PC12, Caco2, and NIH3T3 cells. This growth promoting effect was not shared by other RGS proteins including RGS4, RGS10 and RGS20. Despite its ability to stimulate cell proliferation, RGS19 failed to induce neoplastic transformation in NIH3T3 cells as determined by focus formation and soft-agar assays, and it did not induce tumor growth in athymic nude mice. Deletion mutants of RGS19 lacking the PDZ-binding motif failed to complex with GIPC and did not exhibit any growth promoting effect. Overexpression of GIPC alone in HEK293 cells stimulated cell proliferation whereas its knockdown in H1299 non-small cell lung carcinomas suppressed cell proliferation. This study demonstrates that RGS19, in addition to acting as a GAP, is able to stimulate cell proliferation in a GIPC-dependent manner. (C) 2010 Elsevier Inc. All rights reserved.
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