Max Planck Institute of Molecular Plant Physiology, Am Mühlenberg 1, 14476 Potsdam, Germany.
Department of Biological Sciences, Auburn University, Auburn, AL 36849, USA.
Int J Mol Sci. 2020 Oct 31;21(21):8148. doi: 10.3390/ijms21218148.
The wide natural variation present in rice is an important source of genes to facilitate stress tolerance breeding. However, identification of candidate genes from RNA-Seq studies is hampered by the lack of high-quality genome assemblies for the most stress tolerant cultivars. A more targeted solution is the reconstruction of transcriptomes to provide templates to map RNA-seq reads. Here, we sequenced transcriptomes of ten rice cultivars of three subspecies on the PacBio Sequel platform. RNA was isolated from different organs of plants grown under control and abiotic stress conditions in different environments. Reconstructed de novo reference transcriptomes resulted in 37,500 to 54,600 plant-specific high-quality isoforms per cultivar. Isoforms were collapsed to reduce sequence redundancy and evaluated, e.g., for protein completeness (BUSCO). About 40% of all identified transcripts were novel isoforms compared to the Nipponbare reference transcriptome. For the drought/heat tolerant cultivar N22, 56 differentially expressed genes in developing seeds were identified at combined heat and drought in the field. The newly generated rice transcriptomes are useful to identify candidate genes for stress tolerance breeding not present in the reference transcriptomes/genomes. In addition, our approach provides a cost-effective alternative to genome sequencing for identification of candidate genes in highly stress tolerant genotypes.
水稻中存在广泛的自然变异,这是促进抗逆育种的重要基因来源。然而,由于最具耐逆性的品种缺乏高质量的基因组组装,从 RNA-Seq 研究中鉴定候选基因受到了阻碍。一个更有针对性的解决方案是重建转录组,为 RNA-seq 读取提供图谱模板。在这里,我们在 PacBio Sequel 平台上对三个亚种的 10 个水稻品种进行了转录组测序。从在不同环境下生长的植物的不同器官中分离 RNA,在对照和非生物胁迫条件下进行。重建的从头参考转录组每个品种产生 37500 到 54600 个具有植物特异性的高质量同工型。同工型被合并以减少序列冗余,并进行评估,例如,用于蛋白质完整性(BUSCO)。与 Nipponbare 参考转录组相比,所有鉴定的转录本中约有 40%是新的同工型。对于耐旱/耐热品种 N22,在田间联合热和干旱条件下,发育中的种子中鉴定出 56 个差异表达基因。新生成的水稻转录组可用于鉴定参考转录组/基因组中不存在的耐胁迫育种候选基因。此外,我们的方法为在高度耐胁迫基因型中鉴定候选基因提供了一种具有成本效益的替代基因组测序方法。