Department of Pathogen Molecular Biology, Faculty of Infectious and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK.
J Gen Virol. 2014 Oct;95(Pt 10):2240-2250. doi: 10.1099/vir.0.066647-0. Epub 2014 Jun 30.
The mechanism used by bluetongue virus (BTV) to ensure the sorting and packaging of its 10 genomic segments is still poorly understood. In this study, we investigated the packaging constraints for two BTV genomic segments from two different serotypes. Segment 4 (S4) of BTV serotype 9 was mutated sequentially and packaging of mutant ssRNAs was investigated by two newly developed RNA packaging assay systems, one in vivo and the other in vitro. Modelling of the mutated ssRNA followed by biochemical data analysis suggested that a conformational motif formed by interaction of the 5' and 3' ends of the molecule was necessary and sufficient for packaging. A similar structural signal was also identified in S8 of BTV serotype 1. Furthermore, the same conformational analysis of secondary structures for positive-sense ssRNAs was used to generate a chimeric segment that maintained the putative packaging motif but contained unrelated internal sequences. This chimeric segment was packaged successfully, confirming that the motif identified directs the correct packaging of the segment.
蓝舌病毒(BTV)用于确保其 10 个基因组片段分拣和包装的机制仍知之甚少。在这项研究中,我们研究了两种不同血清型的两个 BTV 基因组片段的包装限制。BTV 血清型 9 的 S4 片段被依次突变,并通过两种新开发的 RNA 包装测定系统(一种在体内,另一种在体外)研究突变 ssRNA 的包装。对突变 ssRNA 进行建模,然后进行生化数据分析,表明分子 5' 和 3' 末端相互作用形成的构象基序对于包装是必需且充分的。在 BTV 血清型 1 的 S8 中也鉴定到了类似的结构信号。此外,还对正链 ssRNA 的二级结构进行了相同的构象分析,生成了一个嵌合片段,该片段保留了假定的包装基序,但包含不相关的内部序列。这个嵌合片段被成功包装,证实了所鉴定的基序可以正确地指导片段的包装。