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正常蚀斑形成需要痘苗病毒中非编码RNA的表达。

Expression of a non-coding RNA in ectromelia virus is required for normal plaque formation.

作者信息

Esteban David J, Upton Chris, Bartow-McKenney Casey, Buller R Mark L, Chen Nanhai G, Schriewer Jill, Lefkowitz Elliot J, Wang Chunlin

出版信息

Virus Genes. 2014 Feb;48(1):38-47. doi: 10.1007/s11262-013-0983-2.

Abstract

Poxviruses are dsDNA viruses with large genomes. Many genes in the genome remain uncharacterized, and recent studies have demonstrated that the poxvirus transcriptome includes numerous so-called anomalous transcripts not associated with open reading frames. Here, we characterize the expression and role of an apparently non-coding RNA in orthopoxviruses, which we call viral hairpin RNA (vhRNA). Using a bioinformatics approach, we predicted expression of a transcript not associated with an open reading frame that is likely to form a stem-loop structure due to the presence of a 21 nt palindromic sequence. Expression of the transcript as early as 2 h post-infection was confirmed by northern blot and analysis of publicly available vaccinia virus infected cell transcriptomes. The transcription start site was determined by RACE PCE and transcriptome analysis, and early and late promoter sequences were identified. Finally, to test the function of the transcript we generated an ectromelia virus knockout, which failed to form plaques in cell culture. The important role of the transcript in viral replication was further demonstrated using siRNA. Although the function of the transcript remains unknown, our work contributes to evidence of an increasingly complex poxvirus transcriptome, suggesting that transcripts such as vhRNA not associated with an annotated open reading frame can play an important role in viral replication.

摘要

痘病毒是具有大基因组的双链DNA病毒。基因组中的许多基因仍未被鉴定,最近的研究表明,痘病毒转录组包括许多与开放阅读框无关的所谓异常转录本。在这里,我们描述了一种在正痘病毒中明显非编码RNA的表达和作用,我们将其称为病毒发夹RNA(vhRNA)。使用生物信息学方法,我们预测了一种与开放阅读框无关的转录本的表达,由于存在21个核苷酸的回文序列,该转录本可能形成茎环结构。通过Northern印迹和对公开可用的痘苗病毒感染细胞转录组的分析,证实了该转录本在感染后2小时就开始表达。通过RACE PCE和转录组分析确定了转录起始位点,并鉴定了早期和晚期启动子序列。最后,为了测试该转录本的功能,我们构建了一种埃可病毒敲除毒株,该毒株在细胞培养中无法形成噬斑。使用siRNA进一步证明了该转录本在病毒复制中的重要作用。尽管该转录本的功能仍然未知,但我们的工作为痘病毒转录组日益复杂的证据做出了贡献,表明诸如vhRNA之类的与注释的开放阅读框无关的转录本可能在病毒复制中发挥重要作用。

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