Lehmann Kathleen C, Gorbalenya Alexander E, Snijder Eric J, Posthuma Clara C
Department of Medical Microbiology, Leiden University Medical Center, Leiden, The Netherlands.
Department of Medical Microbiology, Leiden University Medical Center, Leiden, The Netherlands; Faculty of Bioengineering and Bioinformatics, Lomonosov Moscow State University, Russia.
Virology. 2016 Jan;487:68-74. doi: 10.1016/j.virol.2015.10.002. Epub 2015 Oct 23.
All RNA viruses encode an RNA-dependent RNA polymerase (RdRp), which in arteriviruses is expressed as the C-terminal domain of nonstructural protein 9 (nsp9). Previously, potent primer-dependent RdRp activity has been demonstrated for the homologous polymerase subunit (nsp12) of the distantly related coronaviruses. The only previous study focusing on the in vitro activity of nsp9 of an arterivirus (equine arteritis virus; EAV) reported weak de novo polymerase activity on homopolymeric RNA templates. However, this activity was not retained when Mn(2+) ions were omitted from the assay or when biologically relevant templates were supplied, which prompted us to revisit the biochemical properties of this polymerase. Based on the properties of active-site mutants, we conclude that the RNA-synthesizing activities observed in de novo and primer-dependent polymerase and terminal transferase assays cannot be attributed to recombinant EAV nsp9-RdRp. Our results illustrate the potential pitfalls of characterizing polymerases using highly sensitive biochemical assays.
所有RNA病毒都编码一种依赖RNA的RNA聚合酶(RdRp),在动脉炎病毒中,它作为非结构蛋白9(nsp9)的C末端结构域表达。此前,已证明远亲冠状病毒的同源聚合酶亚基(nsp12)具有强大的依赖引物的RdRp活性。之前唯一一项专注于动脉炎病毒(马动脉炎病毒;EAV)nsp9体外活性的研究报告称,其在同聚RNA模板上的从头聚合酶活性较弱。然而,当测定中省略Mn(2+)离子或提供生物学相关模板时,这种活性无法保留,这促使我们重新审视这种聚合酶的生化特性。基于活性位点突变体的特性,我们得出结论,在从头和依赖引物的聚合酶及末端转移酶测定中观察到的RNA合成活性不能归因于重组EAV nsp9-RdRp。我们的结果说明了使用高度敏感的生化测定来表征聚合酶的潜在陷阱。