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Identification of candidate genes involved in isoquinoline alkaloids biosynthesis in Dactylicapnos scandens by transcriptome analysis

  • Si Mei He
  • , Wan Ling Song
  • , Kun Cong
  • , Xiao Wang
  • , Yang Dong
  • , Jing Cai
  • , Jia Jin Zhang
  • , Guang Hui Zhang
  • , Jian Li Yang
  • , Sheng Chao Yang
  • , Wei Fan
  • Yunnan Agriculture University
  • CAS - Kunming Institute of Zoology
  • University of Chinese Academy of Sciences
  • University of Macau
  • Zhejiang University

科研成果: 期刊稿件文章同行评审

30 引用 (Scopus)

摘要

Dactylicapnos scandens (D. Don) Hutch (Papaveraceae) is a well-known traditional Chinese herb used for treatment of hypertension, inflammation, bleeding and pain for centuries. Although the major bioactive components in this herb are considered as isoquinoline alkaloids (IQAs), little is known about molecular basis of their biosynthesis. Here, we carried out transcriptomic analysis of roots, leaves and stems of D. scandens, and obtained a total of 96,741 unigenes. Based on gene expression and phylogenetic relationship, we proposed the biosynthetic pathways of isocorydine, corydine, glaucine and sinomenine, and identified 67 unigenes encoding enzymes potentially involved in biosynthesis of IQAs in D. scandens. High performance liquid chromatography analysis demonstrated that while isocorydine is the most abundant IQA in D. scandens, the last O-methylation biosynthesis step remains unclear. Further enzyme activity assay, for the first time, characterized a gene encoding O- methyltransferase (DsOMT), which catalyzes O-methylation at C7 of (S)-corytuberine to form isocorydine. We also identified candidate transcription factor genes belonging to WRKY and bHLH families that may be involved in the regulation of IQAs biosynthesis. Taken together, we first provided valuable genetic information for D. scandens, shedding light on candidate genes involved in IQA biosynthesis, which will be critical for further gene functional characterization.

源语言英语
文章编号9119
期刊Scientific Reports
7
1
DOI
出版状态已出版 - 1 12月 2017
已对外发布

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