Expression levels of RGS7 and RGS4 proteins determine the mode of regulation of the G protein-activated K+ channel and control regulation of RGS7 by Gβ5

被引:24
作者
Keren-Raifman, T [1 ]
Bera, AK
Zveig, D
Peleg, S
Witherow, DS
Slepak, VZ
Dascal, N
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Physiol & Pharmacol, IL-69978 Tel Aviv, Israel
[2] Univ Miami, Sch Med, Dept Mol & Cellular Pharmacol, Miami, FL 33101 USA
[3] Univ Miami, Sch Med, Program Neurosci, Miami, FL 33101 USA
关键词
G protein; regulator of G protein signaling; G protein-activated K+ channel; potassium channel; G beta 5; Xenopus oocyte;
D O I
10.1016/S0014-5793(01)02220-7
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
Regulators of G protein signaling RGS4 and RGS7 accelerate the kinetics of K+ channels (GIRKs) in the Xenopus oocyte system. Here, via quantitative analysis of RGS expression, we reveal biphasic effects of RGSs on GIRK regulation, At low concentrations, RGS4 inhibited basal GIRK activity, but stimulated it at high concentrations. RGS7, which is associated with the G protein subunit G beta5, is regulated by G beta5 by two distinct mechanisms. First, G beta5 augments RGS7 activity. and second, it increases its expression. These dual effects resolve previous controversies regarding RGS4 and RGS7 function and indicate that they modulate signaling by mechanisms supplementary to their GTPase-activating protein activity, (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:20 / 28
页数:9
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