Farm Animal Genetic Resources Exploration and Innovation Key Laboratory of Sichuan Province, Sichuan Agricultural University, Chengdu, 611130, China.
Sci Rep. 2017 Aug 9;7(1):7648. doi: 10.1038/s41598-017-08138-z.
It is widely acknowledged that transcriptional diversity largely contributes to biological regulation in eukaryotes. Since the advent of second-generation sequencing technologies, a large number of RNA sequencing studies have considerably improved our understanding of transcriptome complexity. However, it still remains a huge challenge for obtaining full-length transcripts because of difficulties in the short read-based assembly. In the present study we employ PacBio single-molecule long-read sequencing technology for whole-transcriptome profiling in rabbit (Oryctolagus cuniculus). We totally obtain 36,186 high-confidence transcripts from 14,474 genic loci, among which more than 23% of genic loci and 66% of isoforms have not been annotated yet within the current reference genome. Furthermore, about 17% of transcripts are computationally revealed to be non-coding RNAs. Up to 24,797 alternative splicing (AS) and 11,184 alternative polyadenylation (APA) events are detected within this de novo constructed transcriptome, respectively. The results provide a comprehensive set of reference transcripts and hence contribute to the improved annotation of rabbit genome.
人们普遍认为,转录多样性在真核生物的生物调控中起着重要作用。自第二代测序技术问世以来,大量的 RNA 测序研究极大地提高了我们对转录组复杂性的理解。然而,由于基于短读长的组装存在困难,获得全长转录本仍然是一个巨大的挑战。在本研究中,我们采用 PacBio 单分子长读测序技术对兔(Oryctolagus cuniculus)的全转录组进行了分析。我们总共从 14474 个基因座中获得了 36186 条高可信度的转录本,其中超过 23%的基因座和 66%的异构体尚未在当前参考基因组中注释。此外,约 17%的转录本被计算为非编码 RNA。在这个从头构建的转录组中,分别检测到 24797 个剪接(AS)和 11184 个多聚腺苷酸化(APA)事件。这些结果提供了一套全面的参考转录本,有助于提高兔基因组的注释水平。