Dubois Julia, Terrier Olivier, Rosa-Calatrava Manuel
Laboratoire de Virologie et Pathologie Humaine VirPath, Groupe VirCell, Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France.
Laboratoire de Virologie et Pathologie Humaine VirPath, Groupe VirCell, Université Claude Bernard Lyon 1, Université de Lyon, Lyon, France
mBio. 2014 May 13;5(3):e00070-14. doi: 10.1128/mBio.00070-14.
During their nuclear replication stage, influenza viruses hijack the host splicing machinery to process some of their RNA segments, the M and NS segments. In this review, we provide an overview of the current knowledge gathered on this interplay between influenza viruses and the cellular spliceosome, with a particular focus on influenza A viruses (IAV). These viruses have developed accurate regulation mechanisms to reassign the host spliceosome to alter host cellular expression and enable an optimal expression of specific spliced viral products throughout infection. Moreover, IAV segments undergoing splicing display high levels of similarity with human consensus splice sites and their viral transcripts show noteworthy secondary structures. Sequence alignments and consensus analyses, along with recently published studies, suggest both conservation and evolution of viral splice site sequences and structure for improved adaptation to the host. Altogether, these results emphasize the ability of IAV to be well adapted to the host's splicing machinery, and further investigations may contribute to a better understanding of splicing regulation with regard to viral replication, host range, and pathogenesis.
在其核复制阶段,流感病毒会劫持宿主的剪接机制来处理其一些RNA片段,即M段和NS段。在本综述中,我们概述了目前关于流感病毒与细胞剪接体之间这种相互作用的已知知识,特别关注甲型流感病毒(IAV)。这些病毒已经开发出精确的调控机制,重新分配宿主剪接体,以改变宿主细胞表达,并在整个感染过程中实现特定剪接病毒产物的最佳表达。此外,正在进行剪接的IAV片段与人类共有剪接位点高度相似,其病毒转录本显示出值得注意的二级结构。序列比对和共有序列分析以及最近发表的研究表明,病毒剪接位点序列和结构在保守性和进化方面都有所改进,以更好地适应宿主。总之,这些结果强调了IAV适应宿主剪接机制的能力,进一步的研究可能有助于更好地理解与病毒复制、宿主范围和发病机制相关的剪接调控。