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De novo sequencing and analysis of the American ginseng root transcriptome using a GS FLX Titanium platform to discover putative genes involved in ginsenoside biosynthesis

机译:从头测序并使用GS FLX Titanium平台分析西洋参根转录组,以发现参与人参皂苷生物合成的推定基因

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Background American ginseng (Panax quinquefolius L.) is one of the most widely used herbal remedies in the world. Its major bioactive constituents are the triterpene saponins known as ginsenosides. However, little is known about ginsenoside biosynthesis in American ginseng, especially the late steps of the pathway. Results In this study, a one-quarter 454 sequencing run produced 209,747 high-quality reads with an average sequence length of 427 bases. De novo assembly generated 31,088 unique sequences containing 16,592 contigs and 14,496 singletons. About 93.1% of the high-quality reads were assembled into contigs with an average 8-fold coverage. A total of 21,684 (69.8%) unique sequences were annotated by a BLAST similarity search against four public sequence databases, and 4,097 of the unique sequences were assigned to specific metabolic pathways by the Kyoto Encyclopedia of Genes and Genomes. Based on the bioinformatic analysis described above, we found all of the known enzymes involved in ginsenoside backbone synthesis, starting from acetyl-CoA via the isoprenoid pathway. Additionally, a total of 150 cytochrome P450 (CYP450) and 235 glycosyltransferase unique sequences were found in the 454 cDNA library, some of which encode enzymes responsible for the conversion of the ginsenoside backbone into the various ginsenosides. Finally, one CYP450 and four UDP-glycosyltransferases were selected as the candidates most likely to be involved in ginsenoside biosynthesis through a methyl jasmonate (MeJA) inducibility experiment and tissue-specific expression pattern analysis based on a real-time PCR assay. Conclusions We demonstrated, with the assistance of the MeJA inducibility experiment and tissue-specific expression pattern analysis, that transcriptome analysis based on 454 pyrosequencing is a powerful tool for determining the genes encoding enzymes responsible for the biosynthesis of secondary metabolites in non-model plants. Additionally, the expressed sequence tags (ESTs) and unique sequences from this study provide an important resource for the scientific community that is interested in the molecular genetics and functional genomics of American ginseng.
机译:背景西洋参(Panax quinquefolius L.)是世界上使用最广泛的草药之一。它的主要生物活性成分是被称为人参皂甙的三萜皂苷。然而,关于西洋参中人参皂甙生物合成的了解甚少,特别是该途径的后期。结果在这项研究中,四分之一的454测序运行产生了209,747个高质量读段,平均序列长度为427个碱基。从头汇编产生了31,088个唯一序列,其中包含16,592个重叠群和14,496个单例。约93.1%的高质量读段被组装成重叠群,平均覆盖率为8倍。通过针对四个公共序列数据库的BLAST相似性搜索,注释了总共21,684(69.8%)个独特序列,并且《京都议定书》的基因和基因组百科全书将4,097个独特序列分配给了特定的代谢途径。基于上述生物信息学分析,我们发现人参皂苷骨架合成中涉及的所有已知酶,都是通过类异戊二烯途径从乙酰辅酶A开始的。此外,在454个cDNA文库中发现了总共150个细胞色素P450(CYP450)和235个糖基转移酶独特序列,其中一些编码负责将人参皂苷骨架转化为各种人参皂苷的酶。最后,通过茉莉酸甲酯(MeJA)诱导性实验和基于实时PCR分析的组织特异性表达模式分析,选择一种CYP450和四种UDP-糖基转移酶作为最有可能参与人参皂苷生物合成的候选对象。结论我们证明了在MeJA诱导性实验和组织特异性表达模式分析的帮助下,基于454焦磷酸测序的转录组分析是确定负责编码非模型植物次级代谢产物生物合成酶的基因的有力工具。此外,本研究中表达的序列标签(EST)和独特序列为对西洋参的分子遗传学和功能基因组学感兴趣的科学界提供了重要资源。

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