School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510640, People's Republic of China; Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People's Republic of China.
School of Bioscience and Bioengineering, South China University of Technology, Guangzhou 510640, People's Republic of China; Department of Pharmacy, General Hospital of Guangzhou Military Command, Guangzhou 510010, People's Republic of China.
Gene. 2014 Aug 15;547(1):126-35. doi: 10.1016/j.gene.2014.06.041. Epub 2014 Jun 24.
The compound 2,3,5,4'-tetrahydroxy stilbene-2-O-ß-d-glucoside (THSG) synthesized by Fallopia multiflora (F. multiflora) exhibits pharmacological potency. However, the mechanistic details of its biosynthesis pathway are still vague. To clear this ambiguity, we performed de novo transcriptome assembly and digital gene expression (DGE) profiling analyses of F. multiflora using the Illumina RNA-seq system. RNA-seq generated approximately 70 million high-quality reads that were assembled into 65,653 unigenes (mean length=750 bp), including 26,670 clusters and 38,983 singletons. A total of 48,173 (73.4%) unigenes were annotated using public protein databases with a cut-off e-value above 10(-5). Furthermore, we investigated the transcriptome difference of four different F. multiflora tissues using DGE profiling. Variations in gene expression were identified based on comparisons of transcriptomes from various parts of a high-level THSG- and a low-level THSG-producing F. multiflora plant. Clusters with similar differential expression patterns and enriched metabolic pathways with regard to the differentially expressed genes putatively involved in THSG biosynthesis were revealed for the first time. Our data provides the most comprehensive sequence resource regarding F. multiflora so far. Taken together, the results of this study considerably extend the knowledge on THSG production.
虎杖中合成的化合物 2,3,5,4'-四羟基二苯乙烯-2-O-β-D-葡萄糖苷 (THSG) 具有药理学活性。然而,其生物合成途径的机制细节仍不清楚。为了澄清这种模糊性,我们使用 Illumina RNA-seq 系统对虎杖进行了从头转录组组装和数字基因表达 (DGE) 分析。RNA-seq 生成了大约 7000 万个高质量的读数,这些读数被组装成 65653 个非冗余基因 (平均长度=750bp),包括 26670 个聚类和 38983 个单基因。总共 48173 (73.4%) 个非冗余基因使用公共蛋白质数据库进行注释,截止值为 e 值大于 10(-5)。此外,我们使用 DGE 分析研究了四种不同虎杖组织的转录组差异。根据高水平 THSG 和低水平 THSG 产生的虎杖植物不同部位的转录组比较,确定了基因表达的变化。首次揭示了与 THSG 生物合成相关的差异表达基因的类似差异表达模式和富集代谢途径的聚类。我们的数据提供了迄今为止最全面的虎杖序列资源。总之,这项研究的结果极大地扩展了对 THSG 生产的认识。