Single-cell transcriptome atlas of Panax notoginseng embryonic shoot apex: Insights into developmental regulation and triterpene saponin biosynthesis

三七 三萜 转录组 皂甙 生物 生物合成 顶点(几何体) 植物 胚胎干细胞 遗传学 基因 基因表达 医学 病理 替代医学
作者
Mei Liu,Lifang Yang,Junda Guo,Hanye Wang,Saiying Yu,Panpan Wang,Xiuming Cui,Ye Yang,Yuan Liu
出处
期刊:Industrial Crops and Products [Elsevier BV]
卷期号:235: 121820-121820
标识
DOI:10.1016/j.indcrop.2025.121820
摘要

Panax notoginseng , a renowned medicinal herb, accumulates high levels of triterpene saponins, with its secondary metabolites being essential for cardio-cerebrovascular protective effects. While most transcriptome studies have identified key genes involved in developmental regulation and secondary metabolism of P. notoginseng , the spatial and cell-type-specific transcriptional regulation underlying both shoot apex organogenesis and saponins biosynthesis remains unresolved. This knowledge gap primarily stems from the limitations of bulk transcriptomics, which obscures cell-type heterogeneity and spatially restricted regulatory mechanisms. In this study, we constructed the first single-cell transcriptome atlas of the P. notoginseng embryonic shoot apex, resolving 14 transcriptionally distinct subclusters across seven major cell types. Developmental trajectory analysis revealed stage-specific transcriptional programs, with PAMP-triggered immunity-5 ( PTI5 ) and indeterminate-domain 12 ( IDD12 ) emerging as pivotal regulators during early meristematic differentiation. Spatial mapping of saponins biosynthetic pathways identified epidermal and mesophyll cells as primary sites for saponins accumulation, coordinated by cell-type-specific transcription factor families ( NAC , bHLH , MYB , ERF ). This study provides the first systematic framework for understanding how cell-type-specific transcriptional networks orchestrate both developmental trajectory and metabolic specialization in P. notoginseng . These insights not only advance the genetic engineering of high-yielding triterpene saponins cultivars but also establish a paradigm for studying secondary metabolism in non-model medicinal plants. • A single-cell transcriptome atlas of the embryonic shoot apex of P. notoginseng was constructed. • Detailed single-cell transcriptome analysis revealed cellular diversity and developmental trajectories. • Identification of transcription factors PTI5 and IDD12 crucial for early development. • Discovery of gene families and transcription factors regulating triterpene saponin production. • The study will promoting sustainable development of the P. notoginseng industry.
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