Pritlove D C, Poon L L, Devenish L J, Leahy M B, Brownlee G G
Sir William Dunn School of Pathology, University of Oxford, Oxford OX1 3RE, United Kingdom.
J Virol. 1999 Mar;73(3):2109-14. doi: 10.1128/JVI.73.3.2109-2114.1999.
We present evidence, based on extensive mutagenesis, that a hairpin loop at the 5' end of influenza A virus virion RNA (vRNA) is required for the synthesis of polyadenylated mRNA from model vRNA templates in vitro. The hairpin loop, which we term the vRNA 5' hook, contains a stem of 2 bp formed by the second and third residues pairing with the ninth and eighth residues, respectively, and a 4-nucleotide loop composed of the intervening residues 4 to 7. Disruption of the base pairs of the vRNA 5' hook by introducing point mutations prevented polyadenylation, except in two mutants where a G-U base pair reformed. The polyadenylation activity of point mutants could be rescued by constructing double mutants with reformed base pairs in the stem of the vRNA 5' hook. These results suggest that base pairing rather than a particular nucleotide sequence was critical. We also show that mutation of the analogous region in the 3' arm of vRNA did not interfere with the synthesis of polyadenylated mRNA, suggesting that a hook structure in the 3' arm is not required for transcription of polyadenylated mRNA in vitro.
我们基于广泛的诱变实验提供证据表明,甲型流感病毒病毒体RNA(vRNA)5'端的发夹环是体外从模型vRNA模板合成多聚腺苷酸化mRNA所必需的。我们将这个发夹环称为vRNA 5'钩,它包含一个由第二个和第三个残基分别与第九个和第八个残基配对形成的2个碱基对的茎,以及一个由中间的第4至7个残基组成的4个核苷酸的环。通过引入点突变破坏vRNA 5'钩的碱基对会阻止多聚腺苷酸化,但有两个突变体除外,在这两个突变体中重新形成了G-U碱基对。通过构建在vRNA 5'钩茎中具有重新形成碱基对的双突变体,可以挽救点突变体的多聚腺苷酸化活性。这些结果表明碱基配对而非特定的核苷酸序列至关重要。我们还表明,vRNA 3'臂中类似区域的突变不会干扰多聚腺苷酸化mRNA的合成,这表明在体外转录多聚腺苷酸化mRNA时,3'臂中的钩状结构不是必需的。