首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >CLONING AND CHARACTERIZATION OF THE EXTREME 5'-TERMINAL SEQUENCES OF THE RNA GENOMES OF GB VIRUS C HEPATITIS G VIRUS
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CLONING AND CHARACTERIZATION OF THE EXTREME 5'-TERMINAL SEQUENCES OF THE RNA GENOMES OF GB VIRUS C HEPATITIS G VIRUS

机译:GB病毒C型肝炎G病毒RNA基因组的5'-末端极端序列的克隆与鉴定

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摘要

The extreme 5'-terminal sequences of the GB virus C/hepatitis G virus (GBV-C/HGV), containing elements essential for regulation of viral gene expression and replication, have not been determined, By using a RNA-ligase-mediated RACE (rapid amplification of the cDNA ends) procedure, we have cloned the extreme 5'-terminal sequences of the viral genome from the serum of three Taiwanese patients, Sequence analysis of the 5' noncoding region in alignment with one West African and two American isolates showed that (i) a consensus 5'-end sequence was cloned; (ii) about 97% of sequences were homologous among the three Taiwan isolates and also between the two American isolates, whereas about 90% of sequences were homologous among the isolates from the three different geographic areas (iii) the sequence heterogeneity related to geographic separation is confined mainly to three domains: and (iv) a potential hairpin structure, resembling the hairpin structure found in the 5' end of hepatitis C virus genome, was detected in the 5' end of the noncoding region, Our data support the hypotheses that (i) the extreme 5' end of the hepatitis GBV-C/HGV viral genome has been cloned, (ii) there are different genotypes correlated with geographic separation, and (iii) the viral translation and replication mechanisms may be similar to that of hepatitis C virus and pestiviruses. Our data have not only shed light on the viral replication mechanism but also offer information for selection of optimal primer sequences for the detection and genotyping of the hepatitis GBV-C/HGV virus by PCR assays. [References: 22]
机译:通过使用RNA-连接酶介导的RACE,尚未确定GB病毒C / G型肝炎病毒(GBV-C / HGV)的极端5'末端序列,该序列包含调节病毒基因表达和复制所必需的元素(快速扩增cDNA末端)程序,我们从三名台湾患者的血清中克隆了病毒基因组的5'端极端序列,对5'非编码区的序列分析与一株西非和两株美国分离株比对显示(i)克隆了共有的5'-末端序列; (ii)三个台湾分离株之间以及两个美国分离株之间约97%的序列同源,而来自三个不同地理区域的分离株之间约90%的序列同源(iii)与地理分离有关的序列异质性主要限于三个域:(iv)在非编码区的5'端检测到了类似于C型肝炎病毒基因组5'端发现的发夹结构的潜在发夹结构,我们的数据支持以下假设: (i)已克隆出肝炎GBV-C / HGV病毒基因组的极端5'端,(ii)与地理分离相关的不同基因型,(iii)病毒的翻译和复制机制可能与丙型肝炎病毒和瘟病毒。我们的数据不仅阐明了病毒复制机制,而且还为选择最佳引物序列提供信息,这些引物序列用于通过PCR分析检测和检测GBV-C / HGV肝炎病毒的基因型。 [参考:22]

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