Watanabe Masakatsu, Sawada Risa, Aramaki Toshihiro, Skerrett I Martha, Kondo Shigeru
From the Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, Osaka 565-0871, Japan,
From the Graduate School of Frontier Biosciences, Osaka University, 1-3 Yamadaoka, Suita, Osaka 565-0871, Japan.
J Biol Chem. 2016 Jan 15;291(3):1053-63. doi: 10.1074/jbc.M115.673129. Epub 2015 Nov 23.
The zebrafish has a striped skin pattern on its body, and Connexin41.8 (Cx41.8) and Cx39.4 are involved in striped pattern formation. Mutations in these connexins change the striped pattern to a spot or labyrinth pattern. In this study, we characterized Cx41.8 and Cx39.4 after expression in Xenopus oocytes. In addition, we analyzed Cx41.8 mutants Cx41.8I203F and Cx41.8M7, which caused spot or labyrinth skin patterns, respectively, in transgenic zebrafish. In the electrophysiological analysis, the gap junctions formed by Cx41.8 and Cx39.4 showed distinct sensitivity to transjunctional voltage. Analysis of non-junctional (hemichannel) currents revealed a large voltage-dependent current in Cx39.4-expressing oocytes that was absent in cells expressing Cx41.8. Junctional currents induced by both Cx41.8 and Cx39.4 were reduced by co-expression of Cx41.8I203F and abolished by co-expression of Cx41.8M7. In the transgenic experiment, Cx41.8I203F partially rescued the Cx41.8 null mutant phenotype, whereas Cx41.8M7 failed to rescue the null mutant, and it elicited a more severe phenotype than the Cx41.8 null mutant, as evidenced by a smaller spot pattern. Our results provide evidence that gap junctions formed by Cx41.8 play an important role in stripe/spot patterning and suggest that mutations in Cx41.8 can effect patterning by way of reduced function (I203F) and dominant negative effects (M7). Our results suggest that functional differences in Cx41.8 and Cx39.4 relate to spot or labyrinth mutant phenotypes and also provide evidence that these two connexins interact in vivo and in vitro.
斑马鱼身体上有条纹状的皮肤图案,连接蛋白41.8(Cx41.8)和Cx39.4参与条纹图案的形成。这些连接蛋白的突变会将条纹图案改变为斑点或迷宫图案。在本研究中,我们对非洲爪蟾卵母细胞中表达后的Cx41.8和Cx39.4进行了特性分析。此外,我们分析了Cx41.8突变体Cx41.8I203F和Cx41.8M7,它们分别在转基因斑马鱼中导致了斑点或迷宫状皮肤图案。在电生理分析中,由Cx41.8和Cx39.4形成的间隙连接对跨连接电压表现出不同的敏感性。对非连接(半通道)电流的分析显示,在表达Cx39.4的卵母细胞中存在大量电压依赖性电流,而在表达Cx41.8的细胞中则不存在。Cx41.8I203F的共表达降低了由Cx41.8和Cx39.4诱导的连接电流,而Cx41.8M7的共表达则消除了连接电流。在转基因实验中,Cx41.8I203F部分挽救了Cx41.8基因敲除突变体的表型,而Cx41.8M7未能挽救基因敲除突变体,并且它引发了比Cx41.8基因敲除突变体更严重的表型,如较小的斑点图案所示。我们的结果提供了证据,表明由Cx41.8形成的间隙连接在条纹/斑点图案形成中起重要作用,并表明Cx41.8中的突变可通过功能降低(I203F)和显性负效应(M7)影响图案形成。我们的结果表明,Cx41.8和Cx39.4的功能差异与斑点或迷宫突变体表型有关,也提供了证据表明这两种连接蛋白在体内和体外相互作用。