Zhong Y, Wu C F
Department of Biology, University of Iowa, Iowa City 52242.
J Neurosci. 1993 Nov;13(11):4669-79. doi: 10.1523/JNEUROSCI.13-11-04669.1993.
We examined the role of the ether a go-go (eag) gene in modulation of K+ currents and the possibility of its protein product Eag as a subunit in the heteromultimeric assembly of K+ channels by voltage-clamp analysis of larval muscle membrane currents. Previous DNA sequence studies indicate that the eag gene codes for a polypeptide homologous to, but distinct from, the Shaker (Sh) K+ channel subunits (Warmke et al., 1991), and electrophysiological recordings revealed allele-specific effects of eag on four identified K+ currents in Drosophila larval muscles (Zhong and Wu, 1991). Further studies of eag alleles indicated that none of the eag mutations, including alleles producing truncated mRNA messages, eliminate any of the four K+ currents, and that the mutational effects exhibit strong temperature dependence. We found that both W7, an antagonist of Ca2+/calmodulin, and cGMP analogs modulated K+ currents and that their actions were altered or even abolished by eag mutations. These results suggest a role of eag in modulation of K+ currents that may subserve integration of signals at a converging site of the two independent modulatory pathways. The Sh locus is known to encode certain subunits of the IA channel in larval muscle. The existence of multiple eag and Sh alleles enabled an independent test of the idea of Eag as a K+ channel subunit by studying IA in different double-mutant combinations. An array of allele-specific interaction between eag and Sh was observed, which reflects a close association between the Sh and eag subunits within the IA channel. Taken together, our data strengthen the possibility that the eag locus provides a subunit common to different K+ channels. The role of the eag subunit for modulating channels, as opposed to that of Sh subunits required for gating, selectivity, and conductance of the channel, suggest a combinatorial genetic framework for generating diversified K+ channels.
我们通过对幼虫肌肉膜电流进行电压钳分析,研究了超极化激活环核苷酸门控(eag)基因在调节钾离子电流中的作用,以及其蛋白产物Eag作为钾离子通道异源多聚体组装中亚基的可能性。先前的DNA序列研究表明,eag基因编码的多肽与震颤(Sh)钾离子通道亚基同源,但又有所不同(Warmke等人,1991年),并且电生理记录显示eag对果蝇幼虫肌肉中四种已确定的钾离子电流具有等位基因特异性效应(Zhong和Wu,1991年)。对eag等位基因的进一步研究表明,包括产生截短mRNA信息的等位基因在内,没有一个eag突变会消除这四种钾离子电流中的任何一种,并且突变效应表现出强烈的温度依赖性。我们发现,钙调蛋白拮抗剂W7和环鸟苷酸类似物都能调节钾离子电流,并且它们的作用会因eag突变而改变甚至消除。这些结果表明,eag在调节钾离子电流中发挥作用,这可能有助于在两条独立调节途径的汇聚位点整合信号。已知Sh基因座在幼虫肌肉中编码IA通道的某些亚基。通过研究不同双突变组合中的IA,多个eag和Sh等位基因的存在使得能够对Eag作为钾离子通道亚基的观点进行独立测试。观察到eag和Sh之间存在一系列等位基因特异性相互作用,这反映了IA通道内Sh和eag亚基之间的紧密关联。综合来看,我们的数据增强了eag基因座提供不同钾离子通道共有的亚基的可能性。与通道门控、选择性和电导所需的Sh亚基相比,eag亚基在调节通道方面的作用表明存在一个用于产生多样化钾离子通道的组合遗传框架。