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<p>Chili pepper (<i>Capsicum annuum</i> L.) produces specialized metabolites, notably the pungent capsaicin and the red capsanthin. Although their biosynthetic pathways are well characterized, the cellular architecture that underpins spatial regulation remains unclear. Here we present a spatiotemporal single-nucleus atlas of pepper development, integrating single-nucleus RNA sequencing and spatial transcriptomics, profiling 332,468 high-quality cells from 57 samples spanning seedlings to mature fruits. This resource reveals a multilayered organization and precisely maps metabolic genes to defined cell types and spatial regions. We further identify laminar patterning transcription factors, including <i>WRKY6</i>, <i>ZAT10</i> and <i>BTF3</i>, whose layer-specific expression correlates with localized capsanthin accumulation. Our work establishes a framework for dissecting laminar control of specialized metabolism and provides a valuable reference for comparative studies across species. The atlas is openly accessible at <a href="http://Pepper-Cell-Atlas.com">http://Pepper-Cell-Atlas.com</a>.</p>

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Laminar patterning transcription factors orchestrate spatial metabolite partitioning in Capsicum fruit

  • 期刊论文

  • 发表日期：

    2026年5月5日

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  • Jing Han,
  • Yaping Tang,
  • Zhiliang Yue,
  • Wenjun Ji,
  • Keying Geng,
  • Hengjia Yang,
  • Qiqi Jing,
  • Jiahao Xu,
  • Zhi Zhou,
  • Yan Shi,
  • Yuanyuan Miao,
  • Jinshan Li,
  • Yongqi Liu,
  • Chunlei Zhang,
  • Xu Wang,
  • Jigang Li,
  • Zhangsheng Zhu,
  • Shengbao Yang,
  • Bosheng Li

摘要

Chili pepper (Capsicum annuum L.) produces specialized metabolites, notably the pungent capsaicin and the red capsanthin. Although their biosynthetic pathways are well characterized, the cellular architecture that underpins spatial regulation remains unclear. Here we present a spatiotemporal single-nucleus atlas of pepper development, integrating single-nucleus RNA sequencing and spatial transcriptomics, profiling 332,468 high-quality cells from 57 samples spanning seedlings to mature fruits. This resource reveals a multilayered organization and precisely maps metabolic genes to defined cell types and spatial regions. We further identify laminar patterning transcription factors, including WRKY6, ZAT10 and BTF3, whose layer-specific expression correlates with localized capsanthin accumulation. Our work establishes a framework for dissecting laminar control of specialized metabolism and provides a valuable reference for comparative studies across species. The atlas is openly accessible at http://Pepper-Cell-Atlas.com.