禽钙化病毒基因组中由 2 型 IRES 促进的重叠开放阅读框的翻译

Viruses Pub Date : 2024-09-04 DOI:10.3390/v16091413
Yani Arhab, Tatyana V. Pestova, Christopher U. T. Hellen
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引用次数: 0

摘要

钙病毒具有正义 RNA 基因组,通常在长的开放阅读框 1(ORF1)之前具有短的 5′-非翻译区(5′UTR)。例外的是,一些禽类卡里西病毒具有长的 5′UTR,其中含有类似皮卡病毒的内部核糖体进入位点(IRES),这很可能是通过水平基因转移获得的。在这里,我们又发现了许多带有 IRES(主要是 2 型)的禽类钙病毒基因组,并确定其中许多基因组含有一个约 200-300 个密码子长的 ORF(被命名为 ORF1*),与 ORF1 的 5′末端区域重叠。体外翻译证实了来自灰茶色萼状病毒(GTCV)和萼状病毒科 yc-13 分离物(RaCV1)的代表性 2 型 IRES 的活性。图谱显示,在无细胞提取物和体外重组反应中,核糖体起始复合体在 ORF1*起始密码子和 ORF1 中位于 3′ 边界和/或 IRES 下游的一个或两个 AUG 密码子上组装。这三个位点的启动都需要与IRES保守区结合的eIF4A和eIF4G;ORF1*和ORF1主要启动密码子上的启动需要依赖eIF1/eIF1A从IRES的3′边界进行扫描。与 IRES 顶端亚域 Id 结合的 IRES 反式作用因子(ITAFs)Ebp1/ITAF45 以及 PTB(GTCV)或 PCBP2(RaCV1)增强了这些 IRES 的启动。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Translation of Overlapping Open Reading Frames Promoted by Type 2 IRESs in Avian Calicivirus Genomes
Caliciviruses have positive-sense RNA genomes, typically with short 5′-untranslated regions (5′UTRs) that precede the long open reading frame 1 (ORF1). Exceptionally, some avian caliciviruses have long 5′UTRs containing a picornavirus-like internal ribosomal entry site (IRES), which was likely acquired by horizontal gene transfer. Here, we identified numerous additional avian calicivirus genomes with IRESs, predominantly type 2, and determined that many of these genomes contain a ~200–300 codon-long ORF (designated ORF1*) that overlaps the 5′-terminal region of ORF1. The activity of representative type 2 IRESs from grey teal calicivirus (GTCV) and Caliciviridae sp. isolate yc-13 (RaCV1) was confirmed by in vitro translation. Toeprinting showed that in cell-free extracts and in vitro reconstituted reactions, ribosomal initiation complexes assembled on the ORF1* initiation codon and at one or two AUG codons in ORF1 at the 3′-border and/or downstream of the IRES. Initiation at all three sites required eIF4A and eIF4G, which bound to a conserved region of the IRES; initiation on the ORF1* and principal ORF1 initiation codons involved eIF1/eIF1A-dependent scanning from the IRES’s 3′-border. Initiation on these IRESs was enhanced by the IRES trans-acting factors (ITAFs) Ebp1/ITAF45, which bound to the apical subdomain Id of the IRES, and PTB (GTCV) or PCBP2 (RaCV1).
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