Dahl E, Manthey D, Chen Y, Schwarz H J, Chang Y S, Lalley P A, Nicholson B J, Willecke K
Institut für Genetik, Abteilung Molekulargenetik, Universität Bonn, 53117 Bonn, Federal Republic of Germany.
J Biol Chem. 1996 Jul 26;271(30):17903-10. doi: 10.1074/jbc.271.30.17903.
A new gap junction gene isolated from the mouse genome codes for a connexin protein of 261 amino acids. Because of its theoretical molecular mass of 30.366 kDa, it is named connexin-30. Within the connexin gene family, this protein is most closely related to connexin-26 (77% amino acid sequence identity). The coding region of mouse connexin-30 is uninterrupted by introns and is detected in the mouse genome as a single copy gene that is assigned to mouse chromosome 14 by analysis of mouse x hamster somatic cell hybrids. Abundant amounts of connexin-30 mRNA (two transcripts of 2.0 and 2.3 kilobase pairs) were found after 4 weeks of postnatal development in mouse brain and skin. Microinjection of connexin-30 cRNA into Xenopus oocytes induced formation of functional gap junction channels that gated somewhat asymmetrically in response to transjunctional voltage and at significantly lower voltage (Vo = +38 and -46 mV) than the closely homologous connexin-26 channels (Vo = 89 mV). Heterotypic pairings of connexin-30 with connexin-26 and connexin-32 produced channels with highly asymmetric and rectifying voltage gating, respectively. This suggests that the polarity of voltage gating and the cationic selectivity of connexin-30 are similar to those of its closest homologue, connexin-26.
从小鼠基因组中分离出的一个新的间隙连接基因编码一种由261个氨基酸组成的连接蛋白。因其理论分子量为30.366 kDa,故命名为连接蛋白-30。在连接蛋白基因家族中,该蛋白与连接蛋白-26关系最为密切(氨基酸序列同一性为77%)。小鼠连接蛋白-30的编码区无内含子中断,在小鼠基因组中作为单拷贝基因被检测到,通过对小鼠×仓鼠体细胞杂种的分析,该基因被定位到小鼠14号染色体上。在小鼠出生后4周的脑和皮肤中发现了大量的连接蛋白-30 mRNA(两种转录本,分别为2.0和2.3千碱基对)。将连接蛋白-30的cRNA显微注射到非洲爪蟾卵母细胞中可诱导功能性间隙连接通道的形成,这些通道对跨连接电压的响应具有一定的不对称性,且门控电压(Vo = +38和 -46 mV)明显低于密切同源的连接蛋白-26通道(Vo = 89 mV)。连接蛋白-30与连接蛋白-26和连接蛋白-32的异型配对分别产生具有高度不对称和整流电压门控的通道。这表明连接蛋白-30的电压门控极性和阳离子选择性与其最接近的同源物连接蛋白-26相似。