前沿 | 一种拟议中的新 Tombusviridae 属,具有极长的 5' 非翻译区和类似于黄体/霍乱病毒的基因块

IF 2 Q4 VIROLOGY
Zachary Lozier, Lilyahna Hill, Elizabeth Semmann, W. Allen Miller
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引用次数: 0

摘要

古墓病毒科(Tombusviridae)是一个庞大的单链正义 RNA 植物病毒家族,其基因组无封顶、无聚腺苷酸,编码 4-7 个开放阅读框(ORF)。此前,我们通过对玉米和茶树RNA进行高通量测序,发现了一种新的病毒基因组,我们称之为玉米相关古墓病毒(MaTV)。在这里,我们利用 5' 和 3' cDNA 末端快速扩增(RACE)技术确定了 MaTV 基因组的精确末端。在 GenBank 中,我们发现了另外 11 个几乎完整的病毒基因组,它们具有类似 MaTV 的基因组结构和相关的 RNA 依赖性 RNA 聚合酶(RdRp)序列。这些基因组来自不同的植物、真菌、无脊椎动物和脊椎动物,其中一些还在全球多个生物体中发现过。这些基因组现有的 5' 非翻译区(UTR)非常长:至少有 438 至 727 个核苷酸(nt),而其他墓病毒的 5' 非翻译区则小于 150 nt。此外,这些 UTR 含有 6 至 12 个 AUG 三联体,不太可能是起始密码子,因为除了 MaTV 外,5'UTR 中可能没有大的或保守的 ORF。这些特征表明存在一个内部核糖体进入位点(IRES),但我们发现的唯一保守特征是 ORF1 起始密码子上游和邻近的 50 nt 富含胞嘧啶而缺乏鸟苷酸。ORF2(RdRp 基因)似乎是通过对 ORF1 终止密码子的帧内核糖体通读进行翻译的。在所有 12 个基因组中,我们都发现了其他 tombusvirids 中已知的 RNA 结构,以促进这种读通。ORF4 与 ORF3(衣壳蛋白基因)重叠,可能以非 AUG 启动密码子启动。ORF5 预计通过读取 ORF3 终止密码子进行翻译。ORF4 和 ORF5 编码的蛋白质彼此差异很大,与组织结构类似的黄喉病毒和脊髓灰质炎病毒的蛋白质也有很大差异。我们也没有发现明显的 3'帽子独立翻译元件,而这些元件存在于其他墓病毒中。这 12 个基因组与其他 tombusvirids 的基因组差异很大,因此有理由将它们归入一个新属。由于它们含有两个泄漏终止密码子和一个潜在的泄漏起始密码子,我们建议将该属命名为 Rimosavirus(拉丁语中 rimosa = 泄漏)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Frontiers | A proposed new Tombusviridae genus featuring extremely long 5' untranslated regions and a luteo/polerovirus-like gene block
Tombusviridae is a large family of single-stranded, positive-sense RNA plant viruses with uncapped, non-polyadenylated genomes encoding 4–7 open reading frames (ORFs). Previously, we discovered, by high-throughput sequencing of maize and teosinte RNA, a novel genome of a virus we call Maize-associated tombusvirus (MaTV). Here we determined the precise termini of the MaTV genome by using 5’ and 3’ rapid amplification of cDNA ends (RACE). In GenBank, we discovered eleven other nearly complete viral genomes with MaTV-like genome organizations and related RNA-dependent RNA polymerase (RdRp) sequences. These genomes came from diverse plant, fungal, invertebrate and vertebrate organisms, and some have been found in multiple organisms across the globe. The available 5’ untranslated regions (UTRs) of these genomes are remarkably long: at least 438 to 727 nucleotides (nt), in contrast to those of other tombusvirids, which are <150 nt. Moreover these UTRs contain 6 to 12 AUG triplets that are unlikely to be start codons, because - with the possible exception of MaTV - there are no large or conserved ORFs in the 5’ UTRs. Such features suggest an internal ribosome entry site (IRES), but the only conserved features we found were that the 50 nt upstream of and adjacent to the ORF1 start codon are cytosine-rich and guanosine-poor. ORF2 (RdRp gene) appears to be translated by in-frame ribosomal readthrough of the ORF1 stop codon. In all twelve genomes we identified RNA structures known in other tombusvirids to facilitate this readthrough. ORF4 overlaps with ORF3 (coat protein gene) and may initiate with a non-AUG start codon. ORF5 is predicted to be translated by readthrough of the ORF3 stop codon. The proteins encoded by ORFs 4 and 5 diverge highly from each other and from those of the similarly organized luteo- and poleroviruses. We also found no obvious 3’ cap-independent translation elements, which are present in other tombusvirids. The twelve genomes diverge sufficiently from other tombusvirids to warrant classification in a new genus. Because they contain two leaky stop codons and a potential leaky start codon, we propose to name this genus Rimosavirus (rimosa = leaky in Latin).
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