Madhugiri Ramakanth, Fricke Markus, Marz Manja, Ziebuhr John
Institute of Medical Virology, Justus Liebig University Giessen, Schubertstrasse 81, 35392 Giessen, Germany.
Faculty of Mathematics and Computer Science, Friedrich Schiller University Jena, Leutragraben 1, 07743 Jena, Germany.
Virus Res. 2014 Dec 19;194:76-89. doi: 10.1016/j.virusres.2014.10.001. Epub 2014 Oct 13.
Coronavirus genome replication is mediated by a multi-subunit protein complex that is comprised of more than a dozen virally encoded and several cellular proteins. Interactions of the viral replicase complex with cis-acting RNA elements located in the 5' and 3'-terminal genome regions ensure the specific replication of viral RNA. Over the past years, boundaries and structures of cis-acting RNA elements required for coronavirus genome replication have been extensively characterized in betacoronaviruses and, to a lesser extent, other coronavirus genera. Here, we review our current understanding of coronavirus cis-acting elements located in the terminal genome regions and use a combination of bioinformatic and RNA structure probing studies to identify and characterize putative cis-acting RNA elements in alphacoronaviruses. The study suggests significant RNA structure conservation among members of the genus Alphacoronavirus but also across genus boundaries. Overall, the conservation pattern identified for 5' and 3'-terminal RNA structural elements in the genomes of alpha- and betacoronaviruses is in agreement with the widely used replicase polyprotein-based classification of the Coronavirinae, suggesting co-evolution of the coronavirus replication machinery with cognate cis-acting RNA elements.
冠状病毒基因组复制由一个多亚基蛋白复合体介导,该复合体由十几种病毒编码蛋白和几种细胞蛋白组成。病毒复制酶复合体与位于基因组5'和3'末端区域的顺式作用RNA元件之间的相互作用确保了病毒RNA的特异性复制。在过去几年中,冠状病毒基因组复制所需的顺式作用RNA元件的边界和结构已在β冠状病毒中得到广泛表征,在其他冠状病毒属中也有一定程度的研究。在这里,我们综述了目前对位于基因组末端区域的冠状病毒顺式作用元件的理解,并结合生物信息学和RNA结构探测研究,以鉴定和表征α冠状病毒中的假定顺式作用RNA元件。该研究表明,α冠状病毒属成员之间以及不同属之间存在显著的RNA结构保守性。总体而言,在α和β冠状病毒基因组中鉴定出的5'和3'末端RNA结构元件的保守模式与广泛使用的基于复制酶多聚蛋白的冠状病毒亚科分类一致,这表明冠状病毒复制机制与同源顺式作用RNA元件共同进化。