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Acquisition of new protein domains by coronaviruses: analysis of overlapping genes coding for proteins N and 9b in SARS coronavirus

机译:冠状病毒获取新的蛋白质结构域:SARS冠状病毒中编码蛋白质N和9b的重叠基因分析

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摘要

Acquisition of new proteins by viruses usually occurs through horizontal gene transfer or through gene duplication, but another, less common mechanism is the usage of completely or partially overlapping reading frames. A case of acquisition of a completely new protein through introduction of a start codon in an alternative reading frame is the protein encoded by open reading frame (orf) 9b of SARS coronavirus. This gene completely overlaps with the nucleocapsid (N) gene (orf9a). Our findings indicate that the orf9b gene features a discordant codon-usage pattern. We analyzed the evolution of orf9b in concert with orf9a using sequence data of betacoronavirus-lineage b and found that orf9b, which encodes the overprinting protein, evolved largely independent of the overprinted orf9a. We also examined the protein products of these genomic sequences for their structural flexibility and found that it is not necessary for a newly acquired, overlapping protein product to be intrinsically disordered, in contrast to earlier suggestions. Our findings contribute to characterizing sequence properties of newly acquired genes making use of overlapping reading frames.
机译:病毒获得新蛋白质的过程通常是通过水平基因转移或基因复制进行的,但另一种较不常见的机制是使用完全或部分重叠的阅读框。通过在替代阅读框中引入起始密码子获得全新蛋白质的情况是SARS冠状病毒的开放阅读框(orf)9b编码的蛋白质。该基因与核衣壳(N)基因(orf9a)完全重叠。我们的发现表明,orf9b基因具有不协调的密码子使用模式。我们使用beta冠状病毒谱系b的序列数据分析了orf9b与orf9a的进化关系,发现orf9b(其编码叠印蛋白)在很大程度上独立于叠印的orf9a进化。我们还检查了这些基因组序列的蛋白质产物的结构灵活性,发现与先前的建议相反,新获得的重叠蛋白质产物本质上无序是不必要的。我们的发现有助于利用重叠阅读框表征新获得基因的序列特性。

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