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An RNA Element at the 5′-End of the Poliovirus Genome Functions as a General Promoter for RNA Synthesis

机译:脊髓灰质炎病毒基因组5-末端的RNA元件作为RNA合成的一般启动子

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摘要

RNA structures present throughout RNA virus genomes serve as scaffolds to organize multiple factors involved in the initiation of RNA synthesis. Several of these RNA elements play multiple roles in the RNA replication pathway. An RNA structure formed around the 5′- end of the poliovirus genomic RNA has been implicated in the initiation of both negative- and positive-strand RNA synthesis. Dissecting the roles of these multifunctional elements is usually hindered by the interdependent nature of the viral replication processes and often pleiotropic effects of mutations. Here, we describe a novel approach to examine RNA elements with multiple roles. Our approach relies on the duplication of the RNA structure so that one copy is dedicated to the initiation of negative-strand RNA synthesis, while the other mediates positive-strand synthesis. This allows us to study the function of the element in promoting positive-strand RNA synthesis, independently of its function in negative-strand initiation. Using this approach, we demonstrate that the entire 5′-end RNA structure that forms on the positive-strand is required for initiation of new positive-strand RNAs. Also required to initiate positive-strand RNA synthesis are the binding sites for the viral polymerase precursor, 3CD, and the host factor, PCBP. Furthermore, we identify specific nucleotide sequences within “stem a” that are essential for the initiation of positive-strand RNA synthesis. These findings provide direct evidence for a trans-initiation model, in which binding of proteins to internal sequences of a pre-existing positive-strand RNA affects the synthesis of subsequent copies of that RNA, most likely by organizing replication factors around the initiation site.
机译:存在于整个RNA病毒基因组中的RNA结构充当支架,以组织涉及RNA合成起始的多种因素。这些RNA元件中的几种在RNA复制途径中起着多种作用。脊髓灰质炎病毒基因组RNA 5'-末端周围形成的RNA结构与负链和正链RNA合成的启动有关。解剖这些多功能元件的作用通常受病毒复制过程的相互依存性质以及突变的多效性影响。在这里,我们描述了一种新颖的方法来检查具有多种作用的RNA元件。我们的方法依赖于RNA结构的重复,因此一个拷贝专用于起始负链RNA的合成,而另一个则介导正链合成。这使我们能够研究该元素在促进正链RNA合成中的功能,而与它在负链起始中的功能无关。使用这种方法,我们证明了在正链上形成的整个5'端RNA结构是启动新的正链RNA所必需的。启动正链RNA合成还需要病毒聚合酶前体3CD和宿主因子PCBP的结合位点。此外,我们确定了“茎a”内的特定核苷酸序列,这些序列对于启动正链RNA合成至关重要。这些发现为反式启动模型提供了直接的证据,其中蛋白质与预先存在的正链RNA内部序列的结合会影响该RNA后续拷贝的合成,这很可能是通过在起始位点附近组织复制因子来实现的。

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