Wimmers S, Wulfsen I, Bauer C K, Schwarz J R
Abteilung für Angewandte Physiologie, Institut für Physiologie, Universitätsklinikum Hamburg-Eppendorf, Germany.
Pflugers Arch. 2001 Jan;441(4):450-5. doi: 10.1007/s004240000467.
Clonal somato-mammotroph GH3/B6 cells and lactotroph MMQ cells express two (ergl, erg2) of the three cloned rat ether-à-go-go-related gene (erg) K channel subunits. To study whether the erg subunits form heteromultimers, dominant-negative mutants of erg and erg2 were constructed by point mutation (erg1G630S, erg2G480S). After co-expression of these mutants with the wild-type erg1, erg2, or erg3 in Chinese hamster ovary (CHO) cells no erg currents could be detected. In contrast, in co-expression experiments with members of the other ether-à-go-go (EAG) subfamilies (eagl, elkl) the mutant erg1G630S had no effect. These results strongly suggest that erg channel subunits are able to form heteromultimers within the erg channel subfamily. Suppression of the endogenous E-4031-sensitive currents in GH3/B6 and MMQ cells by erg1G630S confirms that they are mediated by erg channels despite the differences in gating kinetics in these cells. Reduction of the erg current in GH3/B6 cells by erg2G480S indicates that erg heteromultimers can also be formed in these cells.
克隆的躯体-促乳素生长激素3/B6细胞和促乳素MMQ细胞表达三种克隆的大鼠外向整流钾通道(erg)亚基中的两种(erg1、erg2)。为了研究erg亚基是否形成异源多聚体,通过点突变构建了erg1和erg2的显性负性突变体(erg1G630S、erg2G480S)。将这些突变体与野生型erg1、erg2或erg3在中国仓鼠卵巢(CHO)细胞中共表达后,未检测到erg电流。相反,在与其他外向整流(EAG)亚家族成员(eag1、elk1)的共表达实验中,突变体erg1G630S没有影响。这些结果强烈表明,erg通道亚基能够在erg通道亚家族内形成异源多聚体。erg1G630S对GH3/B6和MMQ细胞中内源性E-4031敏感电流的抑制作用证实,尽管这些细胞的门控动力学存在差异,但它们是由erg通道介导的。erg2G480S对GH3/B6细胞中erg电流的降低表明,erg异源多聚体也可以在这些细胞中形成。