Cianci C, Tiley L, Krystal M
Department of Virology, Bristol-Myers Squibb Pharmaceutical Research Institute, Wallingford, Connecticut 06492, USA.
J Virol. 1995 Jul;69(7):3995-9. doi: 10.1128/JVI.69.7.3995-3999.1995.
Primary transcripts synthesized by the influenza virus polymerase contain the capped 5' ends of eukaryotic mRNAs. These sequences are derived from host mRNA and scavenged by the viral polymerase as a prerequisite to transcription. The first step in this reaction is the specific binding of the viral polymerase to the cap structure of the host RNA. The role that template RNA plays in this RNA binding reaction was examined in quantitative capped mRNA binding and endonuclease assays. Capped RNA binding was shown to be a template-dependent property of the influenza virus polymerase. Addition of only the 5' end of viral RNA stimulates capped mRNA binding by the viral polymerase, but endonuclease activity requires the addition of the 3' end. The addition of template RNA corresponding to the positive-sense complementary RNA replicative intermediate was also able to stimulate capped mRNA binding but was not able to efficiently activate the viral endonuclease. Thus, regulation of endonuclease activity by the influenza virus polymerase can be dependent on template RNA binding.
流感病毒聚合酶合成的初级转录本包含真核生物mRNA的帽状5'端。这些序列源自宿主mRNA,并被病毒聚合酶清除,作为转录的前提条件。该反应的第一步是病毒聚合酶与宿主RNA的帽结构特异性结合。在定量帽状mRNA结合和核酸内切酶测定中研究了模板RNA在这种RNA结合反应中所起的作用。帽状RNA结合被证明是流感病毒聚合酶的一种模板依赖性特性。仅添加病毒RNA的5'端会刺激病毒聚合酶与帽状mRNA的结合,但核酸内切酶活性需要添加3'端。添加与正链互补RNA复制中间体相对应的模板RNA也能够刺激帽状mRNA结合,但不能有效激活病毒核酸内切酶。因此,流感病毒聚合酶对核酸内切酶活性的调节可能取决于模板RNA结合。