中华水貂长神经毒素同源物的鉴定与克隆。

S R Lin, H B Huang, B N Wu, L S Chang
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引用次数: 7

摘要

采用逆转录-聚合酶链反应,从台湾眼镜蛇的毒腺中分离到细胞RNA,构建了长链神经毒素同源基因cDNA。BLAST在GenBank数据库中搜索序列相似性,发现长神经毒素同源物的cDNA序列与长和短神经毒素的同源性不高。虽然长神经毒素同源物表现出抑制乙酰胆碱诱导的肌肉收缩的活性,但添加长神经毒素同源物所引起的抑制程度仅为添加蛇毒素时的35%左右。此外,长神经毒素同源物的初级结构不满足长或短神经毒素的特征。与其他蛇类的长神经毒素同源物一起,它们可能代表了长神经毒素和短神经毒素之间的进化分歧。
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Characterization and cloning of long neurotoxin homolog from Naja naja atra.

The cDNA encoding a long neurotoxin homolog was constructed from the cellular RNA isolated fom the venom glands of Naja naja atra (Taiwan cobra) by reverse transcription-polymerase chain reaction. BLAST searches for sequence similarity in the GenBank databases reveal that the cDNA sequence of the long neurotoxin homolog is not highly homologous with long and short neurotoxins. Although the long neurotoxin homolog exhibited an activity to inhibit acetylcholine-induced muscle contractions as Naja naja atra cobrotoxin, the degree of inhibition caused by the addition of long neurotoxin homolog was only approximately 35% of that observed with the addition of cobrotoxin. Moreover, the primary structure of the long neurotoxin homolog did not fulfill the characteristic features of long or short neurotoxins. Together with long neurotoxin homologs from other snake species, they probably represent an evolutionary divergence between long and short neurotoxins.

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