Soták Miroslav, Czeranková Odeta, Klein Daniel, Jurčacková Zuzana, Li Ling, Čellárová Eva
Department of Genetics, Institute of Biology and Ecology, Faculty of Science, Pavol Jozef Šafárik University Košice, Slovakia.
Institute of Mathematics, Faculty of Science, Pavol Jozef Šafárik University Košice, Slovakia.
Front Plant Sci. 2016 Jul 13;7:1039. doi: 10.3389/fpls.2016.01039. eCollection 2016.
Next generation sequencing technology rapidly developed research applications in the field of plant functional genomics. Several Hypericum spp. with an aim to generate and enhance gene annotations especially for genes coding the enzymes supposedly included in biosynthesis of valuable bioactive compounds were analyzed. The first de novo transcriptome profiling of Hypericum annulatum Moris, H. tomentosum L., H. kalmianum L., and H. androsaemum L. leaves cultivated in vitro was accomplished. All four species with only limited genomic information were selected on the basis of differences in ability to synthesize hypericins and presence of dark nodules accumulating these metabolites with purpose to enrich genomic background of Hypericum spp. H. annulatum was chosen because of high number of the dark nodules and high content of hypericin. H. tomentosum leaves are typical for the presence of only 1-2 dark nodules localized in the apical part. Both H. kalmianum and H. androsaemum lack hypericin and have no dark nodules. Four separated datasets of the pair-end reads were gathered and used for de novo assembly by Trinity program. Assembled transcriptomes were annotated to the public databases Swiss-Prot and non-redundant protein database (NCBI-nr). Gene ontology analysis was performed. Differences of expression levels in the marginal tissues with dark nodules and inner part of leaves lacking these nodules indicate a potential genetic background for hypericin formation as the presumed site of hypericin biosynthesis is in the cells adjacent to these structures. Altogether 165 contigs in H. annulatum and 100 contigs in H. tomentosum were detected as significantly differentially expressed (P < 0.05) and upregulated in the leaf rim tissues containing the dark nodules. The new sequences homologous to octaketide synthase and enzymes catalyzing phenolic oxidative coupling reactions indispensable for hypericin biosynthesis were discovered. The presented transcriptomic sequence data will improve current knowledge about the selected Hypericum spp. with proposed relation to hypericin biosynthesis and will provide a useful resource of genomic information for consequential studies in the field of functional genomics, proteomics and metabolomics.
下一代测序技术在植物功能基因组学领域迅速发展了研究应用。为了生成和增强基因注释,特别是针对编码可能参与有价值生物活性化合物生物合成的酶的基因,对几种金丝桃属植物进行了分析。完成了对体外培养的环叶金丝桃、绒毛金丝桃、卡氏金丝桃和红果金丝桃叶片的首次从头转录组分析。基于合成金丝桃素能力的差异以及积累这些代谢物的深色结节的存在,选择了这四种基因组信息有限的物种,目的是丰富金丝桃属植物的基因组背景。选择环叶金丝桃是因为其深色结节数量多且金丝桃素含量高。绒毛金丝桃叶片的典型特征是仅在顶端部分有1 - 2个深色结节。卡氏金丝桃和红果金丝桃都缺乏金丝桃素且没有深色结节。收集了四个双端读段的单独数据集,并用于通过Trinity程序进行从头组装。组装后的转录组被注释到公共数据库Swiss - Prot和非冗余蛋白质数据库(NCBI - nr)。进行了基因本体分析。在有深色结节的边缘组织和没有这些结节的叶片内部,表达水平的差异表明了金丝桃素形成的潜在遗传背景,因为推测金丝桃素生物合成的位点在与这些结构相邻的细胞中。在环叶金丝桃中总共检测到165个重叠群,在绒毛金丝桃中检测到100个重叠群,它们在含有深色结节的叶缘组织中显著差异表达(P < 0.05)且上调。发现了与八酮合酶以及金丝桃素生物合成所必需的催化酚类氧化偶联反应的酶同源的新序列。所呈现的转录组序列数据将改善目前关于所选金丝桃属植物与金丝桃素生物合成的拟议关系的知识,并将为功能基因组学、蛋白质组学和代谢组学领域的后续研究提供有用的基因组信息资源。