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首页> 外文期刊>BMC Evolutionary Biology >Molecular cloning and analysis of zebrafish voltage-gated sodium channel beta subunit genes: implications for the evolution of electrical signaling in vertebrates
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Molecular cloning and analysis of zebrafish voltage-gated sodium channel beta subunit genes: implications for the evolution of electrical signaling in vertebrates

机译:斑马鱼电压门控钠通道β亚基基因的分子克隆和分析:对脊椎动物电信号的演变的影响。

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Background Action potential generation in excitable cells such as myocytes and neurons critically depends on voltage-gated sodium channels. In mammals, sodium channels exist as macromolecular complexes that include a pore-forming alpha subunit and 1 or more modulatory beta subunits. Although alpha subunit genes have been cloned from diverse metazoans including flies, jellyfish, and humans, beta subunits have not previously been identified in any non-mammalian species. To gain further insight into the evolution of electrical signaling in vertebrates, we investigated beta subunit genes in the teleost Danio rerio (zebrafish). Results We identified and cloned single zebrafish gene homologs for beta1-beta3 (zbeta1-zbeta3) and duplicate genes for beta4 (zbeta4.1, zbeta4.2). Sodium channel beta subunit loci are similarly organized in fish and mammalian genomes. Unlike their mammalian counterparts, zbeta1 and zbeta2 subunit genes display extensive alternative splicing. Zebrafish beta subunit genes and their splice variants are differentially-expressed in excitable tissues, indicating tissue-specific regulation of zbeta1-4 expression and splicing. Co-expression of the genes encoding zbeta1 and the zebrafish sodium channel alpha subunit Nav1.5 in Chinese Hamster Ovary cells increased sodium current and altered channel gating, demonstrating functional interactions between zebrafish alpha and beta subunits. Analysis of the synteny and phylogeny of mammalian, teleost, amphibian, and avian beta subunit and related genes indicated that all extant vertebrate beta subunits are orthologous, that beta2/beta4 and beta1/beta3 share common ancestry, and that beta subunits are closely related to other proteins sharing the V-type immunoglobulin domain structure. Vertebrate sodium channel beta subunit genes were not identified in the genomes of invertebrate chordates and are unrelated to known subunits of the para sodium channel in Drosophila. Conclusion The identification of conserved orthologs to all 4 voltage-gated sodium channel beta subunit genes in zebrafish and the lack of evidence for beta subunit genes in invertebrate chordates together indicate that this gene family emerged early in vertebrate evolution, prior to the divergence of teleosts and tetrapods. The evolutionary history of sodium channel beta subunits suggests that these genes may have played a key role in the diversification and specialization of electrical signaling in early vertebrates.
机译:背景技术在可激发细胞(如肌细胞和神经元)中动作电位的产生主要取决于电压门控钠通道。在哺乳动物中,钠通道以大分子复合物的形式存在,包括形成孔的α亚基和1个或多个调节性β亚基。尽管已经从包括蝇,水母和人类在内的多种后生动物中克隆了α亚基基因,但以前在任何非哺乳动物物种中都未发现过β亚基。为了进一步了解脊椎动物中电信号的进化,我们研究了硬骨Danio rerio(斑马鱼)中的β亚基基因。结果我们鉴定并克隆了beta1-beta3(zbeta1-zbeta3)的单个斑马鱼基因同源物和beta4(zbeta4.1,zbeta4.2)的重复基因。钠通道β亚基基因座在鱼类和哺乳动物基因组中的组织类似。与它们的哺乳动物对应物不同,zbeta1和zbeta2亚基基因显示出广泛的可变剪接。斑马鱼β亚基基因及其剪接变体在兴奋性组织中差异表达,表明zbeta1-4表达和剪接的组织特异性调节。编码zbeta1和斑马鱼钠通道α亚基Na v 1.5的基因在中国仓鼠卵巢细胞中的共表达增加了钠电流并改变了通道门控,证明了斑马鱼α和β亚基之间的功能相互作用。对哺乳动物,硬骨鱼,两栖动物和鸟类β亚基及相关基因的同系和系统发育分析表明,所有现存的脊椎动物β亚基都是直系同源的,β2/β4和β1/β3具有共同的血统,并且β亚基与其他具有V型免疫球蛋白结构域结构的蛋白质。脊椎动物钠盐通道的基因组中未发现脊椎动物的钠通道β亚基基因,并且与果蝇对钠通道的已知亚基无关。结论斑马鱼中所有4个电压门控钠通道β亚基基因的保守直系同源物的鉴定以及无脊椎动物脊索中β亚基基因的缺乏证据表明,该基因家族出现在脊椎动物进化的早期,然后是硬骨鱼和硬骨鱼。四足动物。钠通道β亚基的进化历史表明,这些基因可能在早期脊椎动物的电信号的多样化和专业化中发挥了关键作用。

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