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De Novo RNA Sequencing and Expression Analysis of Aconitum carmichaelii to Analyze Key Genes Involved in the Biosynthesis of Diterpene Alkaloids

机译:头乌头的从头RNA测序和表达分析,以分析涉及二萜生物碱的生物合成的关键基因。

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Aconitum carmichaelii is an important medicinal herb used widely in China, Japan, India, Korea, and other Asian countries. While extensive research on the characterization of metabolic extracts of A. carmichaelii has shown accumulation of numerous bioactive metabolites including aconitine and aconitine-type diterpene alkaloids, its biosynthetic pathway remains largely unknown. Biosynthesis of these secondary metabolites is tightly controlled and mostly occurs in a tissue-specific manner; therefore, transcriptome analysis across multiple tissues is an attractive method to identify the molecular components involved for further functional characterization. In order to understand the biosynthesis of secondary metabolites, Illumina-based deep transcriptome profiling and analysis was performed for four tissues (flower, bud, leaf, and root) of A. carmichaelii, resulting in 5.5 Gbps clean RNA-seq reads assembled into 128,183 unigenes. Unigenes annotated as possible rate-determining steps of an aconitine-type biosynthetic pathway were highly expressed in the root, in accordance with previous reports describing the root as the accumulation site for these metabolites. We also identified 21 unigenes annotated as cytochrome P450s and highly expressed in roots, which represent candidate unigenes involved in the diversification of secondary metabolites. Comparative transcriptome analysis of A. carmichaelii with A. heterophyllum identified 20,232 orthogroups, representing 30,633 unigenes of A. carmichaelii, gene ontology enrichment analysis of which revealed essential biological process together with a secondary metabolic process to be highly enriched. Unigenes identified in this study are strong candidates for aconitine-type diterpene alkaloid biosynthesis, and will serve as useful resources for further validation studies. View Full-Text
机译:乌头是一种重要的草药,在中国,日本,印度,韩国和其他亚洲国家广泛使用。尽管对卡氏假单胞菌的代谢提取物进行表征的广泛研究表明,包括乌头碱和乌头碱型二萜生物碱在内的许多生物活性代谢物的积累,但其生物合成途径仍然未知。这些次生代谢产物的生物合成受到严格控制,并且大多以组织特异性方式发生。因此,跨多个组织的转录组分析是一种用于鉴定涉及进一步功能表征的分子成分的有吸引力的方法。为了了解次生代谢产物的生物合成,对A. carmichaelii的四个组织(花,芽,叶和根)进行了基于Illumina的深度转录组分析和分析,从而产生了5.5 Gbps的纯净RNA-seq读数,组装成128,183单基因。根据先前的报道,根部被描述为这些代谢产物的积累部位,据报道,乌头碱型生物合成途径的可能的决定速率的步骤的单基因在根中高表达。我们还确定了21个单基因,被标注为细胞色素P450,并在根中高度表达,它们代表了参与次级代谢产物多样化的候选单基因。拟南芥与异叶拟南芥的比较转录组分析确定了20,232个正交群,代表拟南芥的30,633个单基因,其基因本体论富集分析显示必不可少的生物学过程以及次生代谢过程都高度富集。在这项研究中确定的单基因是乌头碱型双萜生物碱生物合成的强候选者,并将作为进一步验证研究的有用资源。查看全文

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