Rohayem Jacques, Jäger Katrin, Robel Ivonne, Scheffler Ulrike, Temme Achim, Rudolph Wolfram
Institut für Virologie, The Calicilab, Medizinisch-Theoretisches Zentrum, Fiedlerstraße 42, D-01307 Dresden, Germany.
Institut für Immunologie, Medizinisch-Theoretisches Zentrum, Fiedlerstraße 42, D-01307 Dresden, Germany.
J Gen Virol. 2006 Sep;87(Pt 9):2621-2630. doi: 10.1099/vir.0.81802-0.
Norovirus (NV) 3D(pol) is a non-structural protein predicted to play an essential role in the replication of the NV genome. In this study, the characteristics of NV 3D(pol) activity and initiation of RNA synthesis have been examined in vitro. Recombinant NV 3D(pol), as well as a 3D(pol) active-site mutant were expressed in Escherichia coli and purified. NV 3D(pol) was able to synthesize RNA in vitro and displayed flexibility with respect to the use of Mg(2+) or Mn(2+) as a cofactor. NV 3D(pol) yielded two different products when incubated with synthetic RNA in vitro: (i) a double-stranded RNA consisting of two single strands of opposite polarity or (ii) the single-stranded RNA template labelled at its 3' terminus by terminal transferase activity. Initiation of RNA synthesis occurred de novo rather than by back-priming, as evidenced by the fact that the two strands of the double-stranded RNA product could be separated, and by dissociation in time-course analysis of terminal transferase and RNA synthesis activities. In addition, RNA synthesis was not affected by blocking of the 3' terminus of the RNA template by a chain terminator, sustaining de novo initiation of RNA synthesis. NV 3D(pol) displays in vitro properties characteristic of RNA-dependent RNA polymerases, allowing the implementation of this in vitro enzymic assay for the development and validation of antiviral drugs against NV, a so far non-cultivated virus and an important human pathogen.
诺如病毒(NV)3D(聚合酶)是一种非结构蛋白,预计在NV基因组复制中起关键作用。在本研究中,已在体外检测了NV 3D(聚合酶)的活性特征和RNA合成起始情况。重组NV 3D(聚合酶)以及一种3D(聚合酶)活性位点突变体在大肠杆菌中表达并纯化。NV 3D(聚合酶)能够在体外合成RNA,并且在使用Mg(2+)或Mn(2+)作为辅因子方面表现出灵活性。当在体外与合成RNA孵育时,NV 3D(聚合酶)产生两种不同的产物:(i)由两条极性相反的单链组成的双链RNA,或(ii)通过末端转移酶活性在其3'末端标记的单链RNA模板。RNA合成起始是从头开始而非通过回引物起始,这由双链RNA产物的两条链可以分离以及在末端转移酶和RNA合成活性的时间进程分析中的解离所证明。此外,RNA合成不受链终止剂对RNA模板3'末端的封闭影响,维持了RNA合成的从头起始。NV 3D(聚合酶)表现出依赖RNA的RNA聚合酶所特有的体外特性,使得这种体外酶测定法可用于开发和验证针对NV的抗病毒药物,NV是一种迄今无法培养的病毒且是重要的人类病原体。