Department of Plant Pathology, University of Nebraska-Lincoln, Lincoln, NE, 68583, USA.
Department of Entomology, University of Nebraska-Lincoln, Lincoln, NE, 68583, USA.
Virology. 2019 Sep;535:20-31. doi: 10.1016/j.virol.2019.06.011. Epub 2019 Jun 17.
High Plains wheat mosaic virus (genus Emaravirus), an octapartite negative-sense RNA virus, encodes two RNA silencing suppressors, P7 and P8. In this study, we found that P7 and P8 efficiently delayed the onset of dsRNA-induced transitive pathway of RNA silencing. Electrophoretic mobility shift assays (EMSA) revealed that only P7 protected long dsRNAs from dicing in vitro and bound weakly to 21- and 24-nt PTGS-like ds-siRNAs. In contrast, P8 bound strongly and relatively weakly to 21- and 24-nt ds-siRNAs, respectively, suggesting size-specific binding. In EMSA, neither protein bound to 180-nt and 21-nt ssRNAs at detectable levels. Sequence analysis revealed that P7 contains a conserved GW motif. Mutational disruption of this motif resulted in loss of suppression of RNA silencing and pathogenicity enhancement, and failure to complement the silencing suppression-deficient wheat streak mosaic virus. Collectively, these data suggest that P7 and P8 proteins utilize distinct mechanisms to overcome host RNA silencing for successful establishment of systemic infection in planta.
高平原小麦花叶病毒(Emaravirus 属)是一种八分体负义 RNA 病毒,编码两种 RNA 沉默抑制子 P7 和 P8。在这项研究中,我们发现 P7 和 P8 能有效地延迟 dsRNA 诱导的 RNA 沉默的转导途径的起始。电泳迁移率变动分析(EMSA)显示,只有 P7 能在体外保护长 dsRNA 免受切割,并与 21- 和 24-nt PTGS 样 ds-siRNA 弱结合。相比之下,P8 分别与 21- 和 24-nt ds-siRNA 结合较强和较弱,表明具有大小特异性结合。在 EMSA 中,两种蛋白均不能以可检测的水平结合 180-nt 和 21-nt ssRNA。序列分析表明 P7 含有一个保守的 GW 基序。该基序的突变破坏导致 RNA 沉默抑制的丧失和致病性增强,并且不能互补沉默抑制缺陷的小麦线条花叶病毒。总的来说,这些数据表明 P7 和 P8 蛋白利用不同的机制来克服宿主的 RNA 沉默,从而在植物体内成功建立系统感染。