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园艺学报 ›› 2026, Vol. 53 ›› Issue (5): 1382-1394.doi: 10.16420/j.issn.0513-353x.2025-1298

• 遗传育种·种质资源·分子生物学 • 上一篇    下一篇

百脉根花后转色中黄酮醇的合成机制

上官巨珑1, 佟林娜3, 魏朝3, 高瑞芳2,3,*()   

  1. 1 吉林农业大学生命科学学院, 长春 130118
    2 吉林大学植物科学学院, 长春 130062
    3 东北师范大学分子表观遗传学教育部重点实验室, 长春 130024
  • 收稿日期:2026-01-16 修回日期:2026-03-23 出版日期:2026-05-25 发布日期:2026-05-26
  • 通讯作者:
  • 基金资助:
    吉林省自然科学基金面上项目(20260102214J)

The Flavonol Biosynthetic Mechanism During Post-Anthesis Color Change in Lotus filicaulis

SHANGGUAN Julong1, TONG Linna3, WEI Chao3, GAO Ruifang2,3,*()   

  1. 1 College of Life ScienceJilin Agricultural University, Changchun 130118, China
    2 College of Plant ScienceJilin University, Changchun 130062, China
    3 Key Laboratory of Molecular Epigenetics of MOENortheast Normal University, Changchun 130024, China
  • Received:2026-01-16 Revised:2026-03-23 Published:2026-05-25 Online:2026-05-26
  • Contact:

摘要:

开花后颜色转变(post-anthesis color change,PACC)是植物优化传粉效率的关键策略,现有研究多聚焦花青素苷驱动机制,黄酮醇的调控作用及与花青素苷的协同关系尚不明确。本研究中以细丝百脉根(Lotus filicaulis)为模型,结合黄酮醇代谢与转录组分析,发现细丝百脉根PACC过程中黄酮醇与花青素苷同步积累,红花期总黄酮醇含量显著升高,且鉴定到两个黄酮醇合酶基因(flavonol synthaseFLSLfFLS1LfFLS2,二者分别在黄花期和红花期高表达。体外酶活试验发现,LfFLS1和LfFLS2均具催化活性,但存在底物偏好性差异:LfFLS1仅利用二氢山奈酚(dihydrokaempferol,DHK)和二氢槲皮素(dihydroquercetin,DHQ),LfFLS2可高效催化三种二氢黄酮醇。为进一步解析FLS差异表达的分子机制,克隆了可能调控FLS表达的MYB转录因子。原生质体瞬时转染试验发现,LfFLS1受第7亚族MYB转录因子LfMYB12与第19亚族MYB转录因子LfMYB21共同激活,LfFLS2仅受LfMYB21调控,两者差异化表达精准匹配PACC不同阶段代谢需求。

关键词: 百脉根, 花色, 黄酮醇, 转录调控

Abstract:

Post-anthesis color change(PACC),a process in which Lotus filicaulis flowers transition from yellow to red,is an adaptive strategy to enhance pollination efficiency. While existing studies have primarily focused on anthocyanins,the regulatory role of flavonols and their synergistic relationship with anthocyanins remain unclear. In this study,flavonol-targeted metabolomics and transcriptomic analyses were integrated to identify flavonols and genes related to flavonol biosynthesis during PACC in L. filicaulis. The functions of flavonol synthaseFLS)genes were validated through prokaryotic enzyme activity assays and transgenic experiments in tobacco. Additionally,transient protoplast transfection assays were employed to investigate the regulatory mechanisms by which MYB transcription factors control FLS expression. The results revealed that flavonols and anthocyanins accumulate synchronously during PACC in L. filicaulis,with total flavonols significantly increased in the red flowers. Two FLS genes,LfFLS1 and LfFLS2,exhibited differential expression patterns:LfFLS1 was highly expressed in yellow flowers,whereas LfFLS2 was specifically upregulated in red flowers. Moreover,both LfFLS proteins displayed catalytic activity but showed distinct substrate preference:LfFLS1 exclusively utilized dihydrokaempferol(DHK)and dihydroquercetin(DHQ),while LfFLS2 efficiently catalyzed all three types of dihydroflavonols. Additionally,LfFLS1 was co-activated by subgroup 7 MYB transcription factor LfMYB12 and subgroup 19 MYB transcription factor LfMYB21,whereas LfFLS2 was exclusively regulated by LfMYB21. This differential expression pattern aligns with the metabolic demands of distinct PACC stages,highlighting a sophisticated regulatory network that modulates flavonol metabolism to support adaptive color transitions.

Key words: Lotus filicaulis, flower color, flavonol, transcription regulation