Identification of a Ras GTPase-activating protein regulated by receptor-mediated Ca2+ oscillations

被引:67
作者
Walker, SA
Kupzig, S
Bouyoucef, D
Davies, LC
Tsuboi, T
Bivona, TG
Cozier, GE
Lockyer, PJ
Buckler, A
Rutter, GA
Allen, MJ
Philips, MR
Cullen, PJ [1 ]
机构
[1] Univ Bristol, Sch Med Sci, Dept Biochem,Inositide Grp, Henry Wellcome Integrated Signalling Labs, Bristol BS8 1TD, Avon, England
[2] NYU, Sch Med, Dept Med Cell Biol & Pharmacol, New York, NY USA
[3] Babraham Inst, Signalling Programme, Cambridge, England
[4] Ardais Corp, Lexington, MA USA
[5] Oxagen Ltd, Oxford, England
基金
英国惠康基金;
关键词
calcium; CAPRI; oscillations; Ras; RASAL;
D O I
10.1038/sj.emboj.7600197
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
Receptor-mediated increases in the concentration of intracellular free calcium ([Ca2+](i)) are responsible for controlling a plethora of physiological processes including gene expression, secretion, contraction, proliferation, neural signalling, and learning. Increases in [Ca2+](i) often occur as repetitive Ca2+ spikes or oscillations. Induced by electrical or receptor stimuli, these repetitive Ca2+ spikes increase their frequency with the amplitude of the receptor stimuli, a phenomenon that appears critical for the induction of selective cellular functions. Here we report the characterisation of RASAL, a Ras GTPase-activating protein that senses the frequency of repetitive Ca2+ spikes by undergoing synchronous oscillatory associations with the plasma membrane. Importantly, we show that only during periods of plasma membrane association does RASAL inactivate Ras signalling. Thus, RASAL senses the frequency of complex Ca2+ signals, decoding them through a regulation of the activation state of Ras. Our data provide a hitherto unrecognised link between complex Ca2+ signals and the regulation of Ras.
引用
收藏
页码:1749 / 1760
页数:12
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