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RNA sequence of astrovirus: distinctive genomic organization and a putative retrovirus-like ribosomal frameshifting signal that directs the viral replicase synthesis.

机译:星状病毒的RNA序列:独特的基因组组织和推定的逆转录病毒样核糖体移码信号,指导病毒复制酶的合成。

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摘要

The genomic RNA of human astrovirus was sequenced and found to contain 6797 nt organized into three open reading frames (1a, 1b, and 2). A potential ribosomal frameshift site identified in the overlap region of open reading frames 1a and 1b consists of a "shifty" heptanucleotide and an RNA stem-loop structure that closely resemble those at the gag-pro junction of some retroviruses. This translation frame-shift may result in the suppression of in-frame amber termination at the end of open reading frame 1a and the synthesis of a nonstructural, fusion polyprotein that contains the putative protease and RNA-dependent RNA polymerase. Comparative sequence analysis indicated that the protease and polymerase of astrovirus are only distantly related to the respective enzymes of other positive-strand RNA viruses. The astrovirus polyprotein lacks the RNA helicase domain typical of other positive-strand RNA viruses of similar genome size. The genomic organization and expression strategy of astrovirus, with the protease and the polymerase brought together by predicted frameshift, most closely resembled those of plant leuteoviruses. Specific features of the sequence and genomic organization support the classification of astroviruses as an additional family of positive-strand RNA viruses, designated Astroviridae.
机译:对人类星状病毒的基因组RNA进行了测序,发现其包含6797 nt,它们被组织成三个开放阅读框(1a,1b和2)。在开放阅读框1a和1b的重叠区域中识别出的潜在核糖体移码位点由“移位”的七核苷酸和RNA茎环结构组成,这些结构与某些逆转录病毒的gag-pro连接处的结构极为相似。这种翻译移码可能会导致开放阅读框1a末端的框内琥珀终止受到抑制,并合成包含推定的蛋白酶和RNA依赖性RNA聚合酶的非结构融合多蛋白。比较序列分析表明,星状病毒的蛋白酶和聚合酶仅与其他正链RNA病毒的各自酶密切相关。星状病毒多蛋白缺乏基因组大小相似的其他正链RNA病毒特有的RNA解旋酶结构域。星状病毒的基因组组织和表达策略,通过预测的移码将蛋白酶和聚合酶结合在一起,最类似于植物麻风病毒。序列的特定特征和基因组组织支持将星状病毒分类为正链RNA病毒的另一家族,称为星状病毒科。

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