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Primary structure, chromosomal localization, and functional expression of a voltage-gated sodium channel from human brain.

机译:来自人脑的电压门控钠通道的一级结构,染色体定位和功能性表达。

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摘要

A cDNA library derived from human cerebral cortex was screened for the presence of sodium channel alpha subunit-specific clones. Ligation of three overlapping clones generated a full-length cDNA clone, HBA, that provided the complete nucleotide sequence coding for a protein of 2005 amino acids. The predicted structure suggests four homologous repeats and exhibits greatest homology and structural similarity to the rat brain sodium channel II. A second cDNA clone, HBB, that encodes a different subtype of sodium channel was isolated. Hybridization of DNA fragments from the 3' untranslated region of HBA and PCR with primers derived from HBB with human-hamster somatic cell hybrids localized these clones to human chromosome 2. In situ hybridization to human metaphase chromosomes mapped the structural genes for both HBA and HBB sodium channels to chromosome 2q23-24.3. The sodium channel HBA gene product was expressed by transfection in CHO cells. Expressed HBA currents were voltage-dependent, sodium-selective, and tetrodotoxin-sensitive and, thus, exhibit the biophysical and pharmacological properties characteristic of sodium channels.
机译:筛选人脑皮质的cDNA文库中钠通道α亚基特异性克隆的存在。三个重叠克隆的连接产生了全长cDNA克隆HBA,该克隆提供了编码2005年氨基酸蛋白质的完整核苷酸序列。预测的结构暗示了四个同源重复,并且与大鼠脑钠通道II表现出最大的同源性和结构相似性。分离出第二个cDNA克隆HBB,其编码不同的钠通道亚型。将HBA 3'非翻译区的DNA片段杂交,并用HBB衍生的引物与人仓鼠体细胞杂种进行PCR杂交,将这些克隆定位于人类染色体2。原位杂交至人类中期染色体,绘制了HBA和HBB的结构基因钠通道到达染色体2q23-24.3。通过在CHO细胞中转染表达钠通道HBA基因产物。表达的HBA电流是电压依赖性,钠选择性和河豚毒素敏感的,因此表现出钠通道的生物物理和药理特性。

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