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HCVE_2/NS_1基因的PCR检测克隆与序列分析
DETECTION,CLONE AND SEOUENCE OF THE PARTIAL E2/NS1 GENE OF HEPATITIS C VIRUS(HCV )IN SEKUM BY RT- PCR
【摘要】 本文报道了利用PCR技术检测了34例丙型肝炎病毒E2/NS1基因的cDNA并与5’非编码区基因的cDNA检测技术进行了比较,应用pUC18质粒对此扩增片段进行了克隆与序列分析,结果表明克隆片段HCV-S1为我国主要流行的HCV基围亚型-II型,其与HCV-II型的核苷酸与氨基酸的同源性均在90%以上,序列分析表明该片段富含脯氨酸和胱氨酸,可能具有复杂的空间构型,且与4个糖基化位点一样保持稳定,另外,在HCV-S1片段的3’端有一36个核苷酸的区域,其变化可能具有型特异性
【Abstract】 The 3’ end fragment of E2/N S1 gene was amplified with polymerase chain reaction(PCR) techni-que and then cloned it to pUC18 vector and sequenced.The results showed the inserted fragment(HCV-S1) had high homology with HCV genotype II,whose nucleotide and amil1oacid homology were morethen 90%. Itwas similar to major epidemic strain in China. The diversity the fragment has beencharacterized .We have also detected 34 hecatitis C cases by RT-pCR using E2 /NS1 gene primers(E2/NS1 PCR)and compared it using 5 ’noncoding region primers(5’NCR PCR)。
【Key words】 Hepatitis C virus(HCV); Hepatitis C; Gene cloning; Gene sequencing Polymerasechain reaction(PCR);
- 【文献出处】 北京医科大学学报 ,JOURNAL OF BEIJING MEDICAL UNIVERSITY , 编辑部邮箱 ,1994年03期
- 【分类号】R373
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