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鉴定黄病毒复制所需的保守的依赖RNA的RNA聚合酶(RdRp)-RNA界面

Identification of a Conserved RNA-dependent RNA Polymerase (RdRp)-RNA Interface Required for Flaviviral Replication.

作者信息

Hodge Kenneth, Tunghirun Chairat, Kamkaew Maliwan, Limjindaporn Thawornchai, Yenchitsomanus Pa-Thai, Chimnaronk Sarin

机构信息

From the Laboratory of RNA Biology, Institute of Molecular Biosciences, Mahidol University, Salaya Campus, Nakhon Pathom 73170 and.

the Department of Anatomy and.

出版信息

J Biol Chem. 2016 Aug 12;291(33):17437-49. doi: 10.1074/jbc.M116.724013. Epub 2016 Jun 22.

Abstract

Dengue virus, an ∼10.7-kb positive-sense RNA virus, is the most common arthropod-communicated pathogen in the world. Despite dengue's clear epidemiological importance, mechanisms for its replication remain elusive. Here, we probed the entire dengue genome for interactions with viral RNA-dependent RNA polymerase (RdRp), and we identified the dominant interaction as a loop-forming ACAG motif in the 3' positive-stranded terminus, complicating the prevailing model of replication. A subset of interactions coincides with known flaviviral recombination sites inside the viral protein-coding region. Specific recognition of the RNA element occurs via an arginine patch in the C-terminal thumb domain of RdRp. We also show that the highly conserved nature of the consensus RNA motif may relate to its tolerance to various mutations in the interacting region of RdRp. Disruption of the interaction resulted in loss of viral replication ability in cells. This unique RdRp-RNA interface is found throughout flaviviruses, implying possibilities for broad disease interventions.

摘要

登革病毒是一种约10.7千碱基对的正链RNA病毒,是世界上最常见的节肢动物传播病原体。尽管登革热具有明确的流行病学重要性,但其复制机制仍不清楚。在这里,我们对整个登革热基因组进行了探测,以寻找与病毒RNA依赖性RNA聚合酶(RdRp)的相互作用,我们确定主要的相互作用是3'正链末端的一个形成环的ACAG基序,这使流行的复制模型变得复杂。一部分相互作用与病毒蛋白质编码区域内已知的黄病毒重组位点重合。RNA元件的特异性识别是通过RdRp C末端拇指结构域中的一个精氨酸区域实现的。我们还表明,共有RNA基序的高度保守性质可能与其对RdRp相互作用区域各种突变的耐受性有关。相互作用的破坏导致细胞中病毒复制能力的丧失。这种独特的RdRp-RNA界面在整个黄病毒中都存在,这意味着有进行广泛疾病干预的可能性。

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