Key Laboratory of Bio-Resources and Eco-Environment of Ministry of Education, College of Life Sciences, Sichuan University, Chengdu, 610065, China.
BGI-Shenzhen, Shenzhen, 518083, China.
Sci Rep. 2018 Feb 19;8(1):3273. doi: 10.1038/s41598-018-21190-7.
RNA alternative splicing (AS) is an important post-transcriptional mechanism enabling single genes to produce multiple proteins. It has been well demonstrated that viruses deploy host AS machinery for viral protein productions. However, knowledge on viral AS is limited to a few disease-causing viruses in model species. Here we report a novel approach to characterizing viral AS using whole transcriptome dataset from host species. Two insect transcriptomes (Acheta domesticus and Planococcus citri) generated in the 1,000 Insect Transcriptome Evolution (1KITE) project were used as a proof of concept using the new pipeline. Two closely related densoviruses (Acheta domesticus densovirus, AdDNV, and Planococcus citri densovirus, PcDNV, Ambidensovirus, Densovirinae, Parvoviridae) were detected and analyzed for AS patterns. The results suggested that although the two viruses shared major AS features, dramatic AS divergences were observed. Detailed analysis of the splicing junctions showed clusters of AS events occurred in two regions of the virus genome, demonstrating that transcriptome analysis could gain valuable insights into viral splicing. When applied to large-scale transcriptomics projects with diverse taxonomic sampling, our new method is expected to rapidly expand our knowledge on RNA splicing mechanisms for a wide range of viruses.
RNA 可变剪接 (AS) 是一种重要的转录后调控机制,可使单个基因产生多种蛋白质。已经充分证明病毒利用宿主 AS 机制来产生病毒蛋白。然而,关于病毒 AS 的知识仅限于少数模式物种中的致病病毒。在这里,我们报告了一种使用宿主物种的全转录组数据集来描述病毒 AS 的新方法。使用新的管道,以 1000 种昆虫转录组进化 (1KITE) 项目中生成的两种昆虫转录组(家蟋蟀和桔实雷氏菌)作为概念验证。检测并分析了两种密切相关的浓核病毒(家蟋蟀浓核病毒、AdDNV 和桔实雷氏菌浓核病毒、PcDNV、双分病毒科、浓核病毒亚科、细小病毒科)的 AS 模式。结果表明,尽管这两种病毒具有主要的 AS 特征,但观察到了明显的 AS 差异。对剪接连接的详细分析显示,病毒基因组的两个区域存在大量的 AS 事件,表明转录组分析可以深入了解病毒剪接。当应用于具有多样化分类学采样的大规模转录组学项目时,我们的新方法有望快速扩展我们对广泛病毒的 RNA 剪接机制的认识。