School of Life Sciences and Center for Soybean Research of the State Key Laboratory of Agrobiotechnology, The Chinese University of Hong Kong, Shatin, Hong Kong Special Administrative Region.
Department of Biology, Faculty of Science, Hong Kong Baptist University, Kowloon Tong, Hong Kong Special Administrative Region.
Nucleic Acids Res. 2020 Aug 20;48(14):7700-7711. doi: 10.1093/nar/gkaa588.
Arabidopsis thaliana transcriptomes have been extensively studied and characterized under different conditions. However, most of the current 'RNA-sequencing' technologies produce a relatively short read length and demand a reverse-transcription step, preventing effective characterization of transcriptome complexity. Here, we performed Direct RNA Sequencing (DRS) using the latest Oxford Nanopore Technology (ONT) with exceptional read length. We demonstrate that the complexity of the A. thaliana transcriptomes has been substantially under-estimated. The ONT direct RNA sequencing identified novel transcript isoforms at both the vegetative (14-day old seedlings, stage 1.04) and reproductive stages (stage 6.00-6.10) of development. Using in-house software called TrackCluster, we determined alternative transcription initiation (ATI), alternative polyadenylation (APA), alternative splicing (AS), and fusion transcripts. More than 38 500 novel transcript isoforms were identified, including six categories of fusion-transcripts that may result from differential RNA processing mechanisms. Aided by the Tombo algorithm, we found an enrichment of m5C modifications in the mobile mRNAs, consistent with a recent finding that m5C modification in mRNAs is crucial for their long-distance movement. In summary, ONT DRS offers an advantage in the identification and functional characterization of novel RNA isoforms and RNA base modifications, significantly improving annotation of the A. thaliana genome.
拟南芥转录组在不同条件下已经得到了广泛的研究和描述。然而,目前大多数的“RNA 测序”技术产生的读长相对较短,并且需要逆转录步骤,这阻碍了对转录组复杂性的有效描述。在这里,我们使用最新的牛津纳米孔技术(ONT)进行了直接 RNA 测序(DRS),具有出色的读长。我们证明,拟南芥转录组的复杂性被大大低估了。ONT 直接 RNA 测序在营养生长阶段(14 天龄的幼苗,阶段 1.04)和生殖阶段(阶段 6.00-6.10)都鉴定到了新的转录本异构体。使用内部开发的名为 TrackCluster 的软件,我们确定了转录起始的替代(ATI)、多聚腺苷酸化的替代(APA)、剪接的替代(AS)和融合转录本。鉴定到超过 38500 个新的转录本异构体,包括六种融合转录本,可能是由不同的 RNA 处理机制导致的。在 Tombo 算法的辅助下,我们发现移动 mRNA 中的 m5C 修饰富集,这与最近发现的 mRNAs 中的 m5C 修饰对于它们的长距离移动至关重要的发现一致。总之,ONT DRS 在鉴定和功能描述新的 RNA 异构体和 RNA 碱基修饰方面具有优势,极大地改善了拟南芥基因组的注释。