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Panicovirus accumulation is governed by two membrane-associated proteins with a newly identified conserved motif that contributes to pathogenicity

机译:盘状病毒的积累受两种膜相关蛋白的控制,这些蛋白具有新鉴定的有助于病原性的保守基序

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Panicum mosaic virus (PMV) has a positive-sense, single-stranded RNA genome that serves as the mRNA for two 5'-proximal genes, p48 and p112. The p112 open reading frame (ORF) has a GDD-motif, a feature of virus RNA-dependent RNA polymerases. Replication assays in protoplasts showed that p48 and p112 are sufficient for replication of PMV and its satellite virus (SPMV). Differential centrifugation of extracts from PMV-infected plants showed that the p48 and p112 proteins are membrane-associated. The same fractions exhibited RNA polymerase activity in vitro on viral RNA templates, suggesting that p48 and p112 represent the viral replication proteins. Moreover, we identified a domain spanning amino acids 306 to 405 on the p48 and p112 PMV ORFs that is common to the Tombusviridae. Alanine scanning mutagenesis of the conserved domain (CD) revealed that several substitutions were lethal or severely debilitated PMV accumulation. Other substitutions did not affect RNA accumulation, yet they caused variable phenotypes suggestive of plant-dependent effects on systemic invasion and symptom induction. The mutants that were most debilitating to PMV replication were hydrophobic amino acids that we hypothesize are important for membrane localization and functional replicase activity.
机译:Panicum花叶病毒(PMV)具有一个正义的单链RNA基因组,可作为两个5'-近端基因p48和p112的mRNA。 p112开放阅读框(ORF)具有GDD基序,这是病毒RNA依赖性RNA聚合酶的特征。原生质体中的复制测定表明p48和p112足以复制PMV及其卫星病毒(SPMV)。来自PMV感染植物的提取物的差异离心显示p48和p112蛋白与膜相关。相同的级分在体外对病毒RNA模板表现出RNA聚合酶活性,表明p48和p112代表病毒复制蛋白。此外,我们确定了一个在跨膜病毒科p48和p112 PMV ORF上跨越306至405位氨基酸的结构域。保守结构域(CD)的丙氨酸扫描诱变显示,一些取代是致死性或严重破坏了PMV的积累。其他取代并没有影响RNA的积累,但是它们引起了可变的表型,暗示了植物对系统侵袭和症状诱导的影响。我们认为最不利于PMV复制的突变体是疏水性氨基酸,对膜定位和功能性复制酶活性很重要。

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