Kang M G, Chen C C, Felix R, Letts V A, Frankel W N, Mori Y, Campbell K P
Howard Hughes Medical Institute, Department of Physiology and Biophysics, University of Iowa College of Medicine, Iowa City, Iowa 52242, USA.
J Biol Chem. 2001 Aug 31;276(35):32917-24. doi: 10.1074/jbc.M100787200. Epub 2001 Jul 5.
A novel gene (Cacng2; gamma(2)) encoding a protein similar to the voltage-activated Ca(2+) channel gamma(1) subunit was identified as the defective gene in the epileptic and ataxic mouse, stargazer. In this study, we analyzed the association of this novel neuronal gamma(2) subunit with Ca(2+) channels of rabbit brain, and the function of the gamma(2) subunit in recombinant neuronal Ca(2+) channels expressed in Xenopus oocytes. Our results showed that the gamma(2) subunit and a closely related protein (called gamma(3)) co-sedimented and co-immunoprecipitated with neuronal Ca(2+) channel subunits in vivo. Electrophysiological analyses showed that gamma(2) co-expression caused a significant decrease in the current amplitude of both alpha(1B)(alpha(1)2.2)-class (36.8%) and alpha(1A)(alpha(1)2.1)-class (39.7%) Ca(2+) channels (alpha(1)beta(3)alpha(2)delta). Interestingly, the inhibitory effects of the gamma(2) subunit on current amplitude were dependent on the co-expression of the alpha(2)delta subunit. In addition, co-expression of gamma(2) or gamma(1) also significantly decelerates the activation kinetics of alpha(1B)-class Ca(2+) channels. Taken together, these results suggest that the gamma(2) subunit is an important constituent of the neuronal Ca(2+) channel complex and that it down-regulates neuronal Ca(2+) channel activity. Furthermore, the gamma(2) subunit likely contributes to the fine-tuning of neuronal Ca(2+) channels by counterbalancing the effects of the alpha(2)delta subunit.
一个编码与电压激活钙通道γ1亚基相似蛋白质的新基因(Cacng2;γ2)被鉴定为癫痫性共济失调小鼠“凝视者”中的缺陷基因。在本研究中,我们分析了这种新的神经元γ2亚基与兔脑钙通道的关联,以及γ2亚基在非洲爪蟾卵母细胞中表达的重组神经元钙通道中的功能。我们的结果表明,γ2亚基和一种密切相关的蛋白质(称为γ3)在体内与神经元钙通道亚基共同沉降并共同免疫沉淀。电生理分析表明,γ2共表达导致α1B(α12.2)类(36.8%)和α1A(α12.1)类(39.7%)钙通道(α1β3α2δ)的电流幅度显著降低。有趣的是,γ2亚基对电流幅度的抑制作用取决于α2δ亚基的共表达。此外,γ2或γ1的共表达也显著减慢了α1B类钙通道的激活动力学。综上所述,这些结果表明γ2亚基是神经元钙通道复合物的重要组成部分,并且它下调神经元钙通道活性。此外,γ2亚基可能通过抵消α2δ亚基的作用,对神经元钙通道进行微调。