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A complex network of RNA–RNA interactions controls subgenomic mRNA transcription in a tombusvirus

机译:RNA-RNA相互作用的复杂网络控制着弓形病毒中的亚基因组mRNA转录

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摘要

Eukaryotic (+)-strand RNA viruses utilize a wide variety of gene expression strategies to achieve regulated production of their viral proteins. A common mechanism used by many is to transcribe viral subgenomic (sg) mRNAs. Transcription of sg mRNA2 in tombusviruses allows for expression of the p19 suppressor of gene silencing and p22 movement proteins. We have investigated the mechanism of transcription of this sg mRNA in Tomato bushy stunt virus and have determined that this process is facilitated by no less than three different RNA modules that are located throughout the viral genome. These RNA units perform distinct tasks and function via long-distance RNA–RNA interactions. Systematic deconstruction of the RNA network and analysis of related RNA promoter elements allowed us to identify fundamental properties necessary for productive sg mRNA2 transcription. Collectively, our results (i) establish specific roles for the different RNA components of a multipartite RNA-based control system, (ii) support a premature termination mechanism for tombusvirus sg mRNA transcription and (iii) reveal a close mechanistic relationship between sg mRNA transcription, viral RNA replication and RNA recombination.
机译:真核(+)链RNA病毒利用多种基因表达策略来实现其病毒蛋白的调控生产。许多人使用的常见机制是转录病毒亚基因组(sg)mRNA。鼓膜病毒中sg mRNA2的转录可表达基因沉默的p19抑制子和p22运动蛋白。我们已经研究了番茄浓密的特技病毒中此sg mRNA转录的机制,并确定整个病毒基因组中存在不少于三个不同的RNA模块可促进此过程。这些RNA单位通过长距离RNA-RNA相互作用执行不同的任务和功能。 RNA网络的系统解构和相关RNA启动子元件的分析使我们能够确定生产性sg mRNA2转录所必需的基本特性。总的来说,我们的结果(i)为基于多部分RNA的控制系统的不同RNA成分建立特定的作用,(ii)支持鼓膜病毒sg mRNA转录的过早终止机制,以及(iii)揭示sg mRNA转录之间的密切机械关系,病毒RNA复制和RNA重组。

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