Tiley L S, Hagen M, Matthews J T, Krystal M
Department of Virology, Bristol-Myers Squibb Pharmaceutical Research Institute, Princeton, New Jersey 08543.
J Virol. 1994 Aug;68(8):5108-16. doi: 10.1128/JVI.68.8.5108-5116.1994.
The enzymatic activity of recombinant influenza virus RNA polymerase is strictly dependent on the addition of a template RNA containing 5' and 3' viral sequences. Here we report the analysis of the binding specificity and physical characterization of the complex by using gel shift, modification interference, and density gradient techniques. The 13S complex binds specifically to short synthetic RNAs that mimic the partially double stranded panhandle structures found at the termini of both viral RNA and cRNA. The polymerase will also bind independently to the single-stranded 5' or 3' ends of viral RNA. It binds most strongly to specific sequences within the 5' end but is unable to bind these sequences in the context of a completely double stranded structure. Modification interference analysis identified the short sequence motifs at the 5' ends of the viral RNA and cRNA templates that are critical for binding.
重组流感病毒RNA聚合酶的酶活性严格依赖于添加含有5'和3'病毒序列的模板RNA。在此,我们报告了通过凝胶迁移、修饰干扰和密度梯度技术对该复合物的结合特异性和物理特性进行的分析。13S复合物特异性结合短的合成RNA,这些RNA模拟了在病毒RNA和cRNA末端发现的部分双链锅柄结构。聚合酶也会独立结合到病毒RNA的单链5'或3'末端。它与5'末端内的特定序列结合最强,但在完全双链结构的情况下无法结合这些序列。修饰干扰分析确定了病毒RNA和cRNA模板5'末端对结合至关重要的短序列基序。