RGS2/G0S8 is a selective inhibitor of Gqα function

SP Heximer, N Watson, ME Linder… - Proceedings of the …, 1997 - National Acad Sciences
SP Heximer, N Watson, ME Linder, KJ Blumer, JR Hepler
Proceedings of the National Academy of Sciences, 1997National Acad Sciences
RGS (r egulators of G protein s ignaling) proteins are GTPase activating proteins that inhibit
signaling by heterotrimeric G proteins. All RGS proteins studied to date act on members of
the Giα family, but not Gsα or G12α. RGS4 regulates Giα family members and Gqα. RGS2
(G0S8) is exceptional because the G proteins it regulates have not been identified. We
report that RGS2 is a selective and potent inhibitor of Gqα function. RGS2 selectively binds
Gqα, but not other Gα proteins (Gi, Go, Gs, G12/13) in brain membranes; RGS4 binds Gqα …
RGS (regulators of G protein signaling) proteins are GTPase activating proteins that inhibit signaling by heterotrimeric G proteins. All RGS proteins studied to date act on members of the Giα family, but not Gsα or G12α. RGS4 regulates Giα family members and Gqα. RGS2 (G0S8) is exceptional because the G proteins it regulates have not been identified. We report that RGS2 is a selective and potent inhibitor of Gqα function. RGS2 selectively binds Gqα, but not other Gα proteins (Gi, Go, Gs, G12/13) in brain membranes; RGS4 binds Gqα and Giα family members. RGS2 binds purified recombinant Gqα, but not Goα, whereas RGS4 binds either. RGS2 does not stimulate the GTPase activities of Gsα or Giα family members, even at a protein concentration 3000-fold higher than is sufficient to observe effects of RGS4 on Giα family members. In contrast, RGS2 and RGS4 completely inhibit Gq-directed activation of phospholipase C in cell membranes. When reconstituted with phospholipid vesicles, RGS2 is 10-fold more potent than RGS4 in blocking Gqα-directed activation of phospholipase Cβ1. These results identify a clear physiological role for RGS2, and describe the first example of an RGS protein that is a selective inhibitor of Gqα function.
National Acad Sciences