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登革病毒RNA复制启动子元件的结构与功能研究

Structural and functional studies of the promoter element for dengue virus RNA replication.

作者信息

Lodeiro María F, Filomatori Claudia V, Gamarnik Andrea V

机构信息

Fundación Instituto Leloir, Buenos Aires, Argentina.

出版信息

J Virol. 2009 Jan;83(2):993-1008. doi: 10.1128/JVI.01647-08. Epub 2008 Nov 12.

Abstract

The 5' untranslated region (5'UTR) of the dengue virus (DENV) genome contains two defined elements essential for viral replication. At the 5' end, a large stem-loop (SLA) structure functions as the promoter for viral polymerase activity. Next to the SLA, there is a short stem-loop that contains a cyclization sequence known as the 5' upstream AUG region (5'UAR). Here, we analyzed the secondary structure of the SLA in solution and the structural requirements of this element for viral replication. Using infectious DENV clones, viral replicons, and in vitro polymerase assays, we defined two helical regions, a side stem-loop, a top loop, and a U bulge within SLA as crucial elements for viral replication. The determinants for SLA-polymerase recognition were found to be common in different DENV serotypes. In addition, structural elements within the SLA required for DENV RNA replication were also conserved among different mosquito- and tick-borne flavivirus genomes, suggesting possible common strategies for polymerase-promoter recognition in flaviviruses. Furthermore, a conserved oligo(U) track present downstream of the SLA was found to modulate RNA synthesis in transfected cells. In vitro polymerase assays indicated that a sequence of at least 10 residues following the SLA, upstream of the 5'UAR, was necessary for efficient RNA synthesis using the viral 3'UTR as template.

摘要

登革病毒(DENV)基因组的5'非翻译区(5'UTR)包含两个对病毒复制至关重要的特定元件。在5'端,一个大的茎环(SLA)结构作为病毒聚合酶活性的启动子。在SLA旁边,有一个短茎环,其中包含一个称为5'上游AUG区域(5'UAR)的环化序列。在这里,我们分析了溶液中SLA的二级结构以及该元件对病毒复制的结构要求。使用感染性DENV克隆、病毒复制子和体外聚合酶测定,我们确定了SLA内的两个螺旋区域、一个侧茎环、一个顶环和一个U凸起是病毒复制的关键元件。发现SLA-聚合酶识别的决定因素在不同的DENV血清型中是常见的。此外,DENV RNA复制所需的SLA内的结构元件在不同的蚊媒和蜱媒黄病毒基因组中也保守,这表明黄病毒在聚合酶-启动子识别方面可能有共同策略。此外,发现SLA下游存在的一个保守的寡聚(U)序列可调节转染细胞中的RNA合成。体外聚合酶测定表明,以病毒3'UTR为模板进行有效RNA合成时,SLA之后、5'UAR上游至少10个残基的序列是必需的。

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