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Accumulation mechanism of metabolite markers identified by machine learning between Qingyuan and Xiushui counties in Polygonatum cyrtonema Hua. | LitMetric

AI Article Synopsis

  • Polygonatum cyrtonema Hua is a traditional Chinese medicinal plant valued for its potential in treating diabetes and chronic diseases, primarily due to its rhizomes containing beneficial secondary metabolites like flavonoids and saponins.
  • A study identified 482 metabolites from rhizomes in two different regions, revealing distinct profiles through cluster analysis and employing machine learning techniques to pinpoint specific metabolite markers.
  • Further analysis, including transcriptomics and functional assays, highlighted key genes linked to the biosynthesis of important compounds, offering insights for enhancing the production of these therapeutic metabolites.

Article Abstract

Polygonatum cyrtonema Hua is a traditional Chinese medicinal plant acclaimed for its therapeutic potential in diabetes and various chronic diseases. Its rhizomes are the main functional parts rich in secondary metabolites, such as flavonoids and saponins. But their quality varies by region, posing challenges for industrial and medicinal application of P. cyrtonema. In this study, 482 metabolites were identified in P. cyrtonema rhizome from Qingyuan and Xiushui counties. Cluster analysis showed that samples between these two regions had distinct secondary metabolite profiles. Machine learning methods, specifically support vector machine-recursive feature elimination and random forest, were utilized to further identify metabolite markers including flavonoids, phenolic acids, and lignans. Comparative transcriptomics and weighted gene co-expression analysis were performed to uncover potential candidate genes including CHI, UGT1, and PcOMT10/11/12/13 associated with these compounds. Functional assays using tobacco transient expression system revealed that PcOMT10/11/12/13 indeed impacted metabolic fluxes of the phenylpropanoid pathway and phenylpropanoid-related metabolites such as chrysoeriol-6,8-di-C-glucoside, syringaresinol-4'-O-glucopyranosid, and 1-O-Sinapoyl-D-glucose. These findings identified metabolite markers between these two regions and provided valuable genetic insights for engineering the biosynthesis of these compounds.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10916035PMC
http://dx.doi.org/10.1186/s12870-024-04871-6DOI Listing

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