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首页> 外文期刊>The Journal of Comparative Neurology >Expression pattern of the ether-a-go-go-related (ERG) family proteins in the adult mouse central nervous system: Evidence for coassembly of different subunits.
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Expression pattern of the ether-a-go-go-related (ERG) family proteins in the adult mouse central nervous system: Evidence for coassembly of different subunits.

机译:成年小鼠中枢神经系统中与醚相关的(ERG)家族蛋白的表达模式:不同亚基共组装的证据。

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Voltage-dependent K(+) channels are the main determinants in controlling cellular excitability within the central nervous system. Among voltage-dependent K(+) channels, the ERG subfamily is deeply involved in the control of cellular excitability, both in mammals and in invertebrates. ERG channels are encoded by different genes: the erg1 gene, which can generate two alternative transcripts (erg1a and erg1b), erg2 and erg3. The aim of the present study was to determine the expression pattern and cellular localization of ERG proteins (ERG1, ERG2, and ERG3) in the mouse CNS, differentiating, for the first time, the ERG1A and ERG1B isoforms. To this purpose, novel specific antibodies were raised against the various channel proteins and their specificity and immunoreactivity tested. It emerged that: 1) all the erg genes were indeed translated in neuronal tissue; 2) ERG proteins distribution in the mouse CNS often overlapped, and only in specific areas each ERG protein showed a distinct pattern of expression;and 3) ERG proteins were generally expressed in neuronal soma, but dendritic and/or white matter labeling could be detected in specific areas. The finding that ERG proteins often have an overlapping expression suggests that neuronal ERG currents could be determined, at least in part, by heterotetrameric ERG channels. This suggestion is demonstrated to occur for ERG1A/ERG1B by showing that the two isoforms coassemble in mouse brain. J. Comp. Neurol. 491:157-174, 2005. (c) 2005 Wiley-Liss, Inc.
机译:电压依赖性K(+)通道是控制中枢神经系统内细胞兴奋性的主要决定因素。在电压依赖性K(+)通道中,ERG亚家族在哺乳动物和无脊椎动物中都深深地参与了细胞兴奋性的控制。 ERG通道由不同的基因编码:erg1基因,它可以生成两个替代的转录本(erg1a和erg1b),erg2和erg3。本研究的目的是确定小鼠CNS中ERG蛋白(ERG1,ERG2和ERG3)的表达模式和细胞定位,首次区分出ERG1A和ERG1B亚型。为了这个目的,产生了针对各种通道蛋白的新型特异性抗体,并对其特异性和免疫反应性进行了测试。结果表明:1)所有erg基因确实在神经元组织中翻译; 2)ERG蛋白在小鼠中枢神经系统中的分布经常重叠,并且每个ERG蛋白仅在特定区域显示出不同的表达模式;和3)ERG蛋白通常在神经元体中表达,但是可以检测到树突状和/或白质标记在特定区域。 ERG蛋白通常具有重叠表达的发现表明,神经元ERG电流可以至少部分地由异四聚体ERG通道确定。通过显示这两种同工型在小鼠大脑中共装配,表明ERG1A / ERG1B出现了这一建议。 J.比较神经元。 491:157-174,2005.(c)2005 Wiley-Liss,Inc.

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