Biology Department, University of Nebraska at Omaha, Omaha, Nebraska, USA.
Biology Department, University of Nebraska at Omaha, Omaha, Nebraska, USA
J Virol. 2019 Nov 13;93(23). doi: 10.1128/JVI.01288-19. Print 2019 Dec 1.
Enteroviral RNA genomes share a long, highly structured 5' untranslated region (5' UTR) containing a type I internal ribosome entry site (IRES). The 5' UTR is composed of stably folded RNA domains connected by unstructured RNA regions. Proper folding and functioning of the 5' UTR underlies the efficiency of viral replication and also determines viral virulence. We have characterized the structure of 5' UTR genomic RNA from coxsackievirus B3 using selective 2'-hydroxyl acylation analyzed by primer extension (SHAPE) and base-specific chemical probes in solution. Our results revealed novel structural features, including realignment of major domains, newly identified long-range interactions, and an intrinsically disordered connecting region. Together, these newly identified features contribute to a model for enteroviral 5' UTRs with type I IRES elements that links structure to function during the hierarchical processes directed by genomic RNA during viral infection. Enterovirus infections are responsible for human diseases, including myocarditis, pancreatitis, acute flaccid paralysis, and poliomyelitis. The virulence of these viruses depends on efficient recognition of the RNA genome by a large family of host proteins and protein synthesis factors, which in turn relies on the three-dimensional folding of the first 750 nucleotides of the molecule. Structural information about this region of the genome, called the 5' untranslated region (5' UTR), is needed to assist in the process of vaccine and antiviral development. This work presents a model for the structure of the enteroviral 5' UTR. The model includes an RNA element called an intrinsically disordered RNA region (IDRR). Intrinsically disordered proteins (IDPs) are well known, but correlates in RNA have not been proposed. The proposed IDRR is a 20-nucleotide region, long known for its functional importance, where structural flexibility helps explain recognition by factors controlling multiple functional states.
肠病毒 RNA 基因组具有一个长的、高度结构化的 5'非翻译区(5'UTR),其中包含一个 I 型内部核糖体进入位点(IRES)。5'UTR 由稳定折叠的 RNA 结构域通过非结构化的 RNA 区域连接而成。5'UTR 的正确折叠和功能是病毒复制效率的基础,也决定了病毒的毒力。我们使用选择性 2'-羟基酰化分析引物延伸(SHAPE)和溶液中的碱基特异性化学探针,对柯萨奇病毒 B3 的 5'UTR 基因组 RNA 结构进行了表征。我们的结果揭示了新的结构特征,包括主要结构域的重新排列、新发现的长程相互作用和固有无序的连接区。这些新发现的特征共同构成了一个具有 I 型 IRES 元件的肠病毒 5'UTR 模型,该模型将结构与病毒感染过程中基因组 RNA 指导的分层过程中的功能联系起来。肠病毒感染可导致人类疾病,包括心肌炎、胰腺炎、急性弛缓性麻痹和脊髓灰质炎。这些病毒的毒力取决于宿主蛋白和蛋白质合成因子对 RNA 基因组的有效识别,而这又依赖于分子前 750 个核苷酸的三维折叠。该基因组区域的结构信息,称为 5'非翻译区(5'UTR),对于协助疫苗和抗病毒药物的开发是必要的。这项工作提出了一个肠病毒 5'UTR 的结构模型。该模型包括一个称为固有无序 RNA 区(IDRR)的 RNA 元件。众所周知,固有无序蛋白(IDP)是存在的,但在 RNA 中尚未提出相关性。所提出的 IDRR 是一个 20 个核苷酸的区域,其功能重要性早已为人所知,其结构灵活性有助于解释其对控制多种功能状态的因子的识别。