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Structure-function analysis of the 3' stem-loop of hepatitis C virus genomic RNA and its role in viral RNA replication.

机译:丙型肝炎病毒基因组RNA 3'茎环的结构功能分析及其在病毒RNA复制中的作用。

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Previous studies indicate that the 3' terminal 46 nt of the RNA genome of hepatitis C virus (HCV) are highly conserved among different viral strains and essential for RNA replication. Here, we describe a mutational analysis of the 3' terminal hairpin (stem-loop I) that is putatively formed by this sequence and demonstrate its role in replication of the viral RNA. We show that single base substitutions within the 6-nt loop at positions adjacent to the stem abrogate replication of a subgenomic RNA, whereas substitutions in the three apical nucleotides were well tolerated without loss of replication competence. Single point mutations were also well tolerated within the middle section of the duplex, but not at the penultimate nucleotide positions near either end of the stem. However, complementary substitutions at the -19 and -28 positions (from the 3' end) restored replication competence, providing strong evidence for the existence of the structure and its involvement in RNA replication. This was confirmed by rescue of replicating RNAs from mutants containing complementary 10-nt block substitutions at the base of the stem. Each of these RNAs contained an additional U at the 3' terminus. Further experiments indicated a strong preference for U at the 3' terminal position (followed in order by C, A, and G), and a G at the -2 position. These features of stem-loop I are likely to facilitate recognition of the 3' end of the viral RNA by the viral RNA replicase.
机译:先前的研究表明,丙型肝炎病毒(HCV)RNA基因组的3'末端46 nt在不同病毒株之间高度保守,并且对于RNA复制至关重要。在这里,我们描述了由该序列推定形成的3'末端发夹(茎环I)的突变分析,并证明了其在病毒RNA复制中的作用。我们表明,在6-nt环内邻近碱基的单碱基取代消除了亚基因组RNA的复制,而在三个顶端核苷酸中的取代被很好地耐受,而没有复制能力的损失。在双链体的中间部分,单点突变也具有良好的耐受性,但在茎的任一端附近的倒数第二个核苷酸位置却没有。但是,在-19和-28位(从3'端开始)的互补取代恢复了复制能力,为该结构的存在及其参与RNA复制提供了有力的证据。通过挽救从茎基部包含互补10-nt嵌段取代的突变体复制RNA的方法,可以证实这一点。这些RNA中的每一个在3'末端都包含一个额外的U。进一步的实验表明,在3'末端位置(依次为C,A和G)非常喜欢U,在-2位置则优先选择G。茎环I的这些特征可能有助于通过病毒RNA复制酶识别病毒RNA的3'末端。

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