4.7 Article

Integrative analysis of the steroidal alkaloids distribution and biosynthesis of bulbs Fritillariae Cirrhosae through metabolome and transcriptome analyses

Journal

BMC GENOMICS
Volume 23, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s12864-022-08724-0

Keywords

Fritillaria cirrhosa; Liliaceae; Steroidal alkaloid biosynthesis; Metabolomics; Transcriptome

Funding

  1. Sichuan Provincial Science Fund for Distinguished Young Scholars [22JCQN0006]
  2. Aba Autonomous Prefecture application technology [R22YYJSYJ0015]
  3. State Key Laboratory of Southwestern Chinese Medicine Resources [SCMR202103]
  4. Natural Science Foundation of Sichuan Province [2022NSFSC0583]

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In this study, non-target metabolomics and transcriptome analysis were performed on Bulbus Fritillariae Cirrhosae (BFC) and Bulbus Fritillariae Thunbergia (BFT). The results showed higher levels of steroidal alkaloids in BFC compared to BFT, and differentially expressed genes potentially involved in alkaloid biosynthesis were identified.
Background Bulbus Fritillariae Cirrhosae (BFC) is an endangered high-altitude medicine and food homology plant with anti-tumor, anti-asthmatic, and antitussive activities as it contains a variety of active ingredients, especially steroidal alkaloids. Bulbus Fritillariae Thunbergia (BFT) is another species of Fritillaria that grows at lower altitude areas. Production of plant-derived active ingredients through a synthetic biology strategy is one of the current hot topics in biological research, which requires a complete understanding of the related molecular pathways. Our knowledge of the steroidal alkaloid biosynthesis in Fritillaria species is still very limited. Results To promote our understanding of these pathways, we performed non-target metabolomics and transcriptome analysis of BFC and BFT. Metabolomics analysis identified 1288 metabolites in BFC and BFT in total. Steroidal alkaloids, including the proposed active ingredients of Fritillaria species peimine, peimisine, peiminine, etc., were the most abundant alkaloids detected. Our metabolomics data also showed that the contents of the majority of the steroidal alkaloids in BFC were higher than in BFT. Further, our comparative transcriptome analyses between BFC and BFT identified differentially expressed gene sets among these species, which are potentially involved in the alkaloids biosynthesis of BFC. Conclusion These findings promote our understanding of the mechanism of steroidal alkaloids biosynthesis in Fritillaria species.

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