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P7 and P8 proteins of High Plains wheat mosaic virus, a negative-strand RNA virus, employ distinct mechanisms of RNA silencing suppression

机译:P7和P8蛋白的高平原小麦马赛克病毒,一种负链RNA病毒,采用不同的RNA沉默抑制机制

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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.
机译:高平原小麦马赛克病毒(emaravirus),八大公共术负感染RNA病毒,编码两个RNA沉默抑制器,P7和P8。在这项研究中,我们发现P7和P8有效地延迟了DSRNA诱导的RNA沉默的递动路径的发作。电泳迁移率移位测定(EMSA)揭示仅P7在体外切割的L长DSRNA受到影响,并将弱至21-和24-NT PTGS样DS-siRNA。相比之下,P8分别对21-和24-NT DS-siRNA相对较大,暗示尺寸特异性结合。在EMSA中,在可检测水平下均未结合180-NT和21-NT SSRNA。序列分析显示P7含有保守的GW主题。该基序的突变破坏导致抑制RNA沉默和致病性增强的抑制,并且未能补充沉默抑制缺乏小麦条纹马赛克病毒。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RNA沉默,以便成功建立植物系统感染。

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