Yi Minkyung, Lemon Stanley M
Department of Microbiology and Immunology, The University of Texas Medical Branch at Galveston, Galveston, Texas 77555-1019, USA.
RNA. 2003 Mar;9(3):331-45. doi: 10.1261/rna.2144203.
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.
先前的研究表明,丙型肝炎病毒(HCV)RNA基因组的3'末端46个核苷酸在不同病毒株中高度保守,且对RNA复制至关重要。在此,我们描述了对由该序列推定形成的3'末端发夹结构(茎环I)的突变分析,并证明了其在病毒RNA复制中的作用。我们发现,茎相邻位置的6核苷酸环内的单碱基替换会消除亚基因组RNA的复制,而三个顶端核苷酸的替换则能很好地耐受,且不丧失复制能力。双链中间部分的单点突变也能很好地耐受,但在茎两端附近的倒数第二个核苷酸位置则不能。然而,在-19和-28位置(从3'端起)的互补替换恢复了复制能力,有力地证明了该结构的存在及其参与RNA复制。这通过从茎基部含有互补10核苷酸阻断替换的突变体中拯救复制RNA得到证实。这些RNA中的每一个在3'末端都额外含有一个U。进一步的实验表明,3'末端位置强烈偏好U(依次为C、A和G),-2位置偏好G。茎环I的这些特征可能有助于病毒RNA复制酶识别病毒RNA的3'末端。