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作 者:魏来[1] 潘修成 吴文漪 王宇[1] 陶其敏[1]
机构地区:[1]北京医科大学肝病研究所
出 处:《徐州医学院学报》1998年第2期87-89,共3页Acta Academiae Medicinae Xuzhou
基 金:国家自然科学基金;江苏省委333工程基金;江苏省教委自然科学基金
摘 要:目的分析丙型肝炎病毒(HCV)非结构基因5b(NS5b)区部分核苷酸序列特征。方法以逆转录巢式聚合酶链反应获得位于7918位至8293位间的cDNA片段,克隆后测定重组子序列,计算机分析其特征。结果获得了376碱基对长的HCVNS5b基因(HC-P39),与HCV-1,HC-C2,HCV-J,HCV-BK,HCV-J6及HC-J8相比,核苷酸水平的同源性分别为76.97%,88.92%,87.75%,89.21%,63.85%及64.43%。在核苷酸8111位至核苷酸8124位发现一个新的移码突变,并因此在核苷酸8122位形成一个终止突变。结论在HCVNS5b区发现一个新的移码突变。Objective To analyse the nucleotide sequence of nonstructural 5b genome (NS5b) of hepatitis C virus (HCV). Methods The cDNA segment of HCV ranged from position 7918 to position 8293 was obtained by reverse transcription nested polymerase chain reaction (RT-PCR) , and was then cloned and sequenced. Results The genome obtained, containing 376 bp and corresponding to HCV NS5b, was designated as HC-P39. It was found that HC-P39 shared 76.97%,88.92%,87.75%,89.21%,63.85% and 64.43% nucleotide homology with HCV-1, HC-C2, HCV-J, HCV-BK, HC-J6 and HC-J8 respectively, and hence belonged to genotype Ⅱ/1b. Comparison of HC-P39 with the 6 reported genotypes revealed there was a novel frame-shift mutation between position 8111 and position 8124, which was ended by the introduction of an in-frame stop codon beginning from position 8122. Conclusion A novel frame-shift mutation in HCV NS5b genome was recognized through the study.
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