生物技术通报 ›› 2026, Vol. 42 ›› Issue (3): 302-311.doi: 10.13560/j.cnki.biotech.bull.1985.2025-0535

• 研究报告 • 上一篇    下一篇

脱落酸与乙烯协同调控薄皮甜瓜果实软化的机制

陈常璐1(), 杨志芳1, 曹嵩晓2, 李杨青1, 叶靖烽1, 吕海艳1, 陈姗姗1, 陈昊1()   

  1. 1.吉林农业大学园艺学院,长春 130000
    2.日照市东港区农业农村局,日照 276800
  • 收稿日期:2025-05-25 出版日期:2026-03-26 发布日期:2026-04-23
  • 通讯作者: 陈昊,男,博士,讲师,研究方向 :甜瓜设施栽培与生理;E-mail: haoc@jlau.edu.cn
  • 作者简介:陈常璐,女,硕士,研究方向 :甜瓜设施栽培与生理;E-mail: 1148402745@qq.com
  • 基金资助:
    国家自然科学基金青年科学基金项目(31902040);吉林省教育厅科学技术研究项目(JJKH20240445KJ)

Mechanism of Abscisic Acid and Ethylene Collaboratively Regulating the Softening of Oriental Melon Fruits

CHEN Chang-lu1(), YANG Zhi-fang1, CAO Song-xiao2, LI Yang-qing1, YE Jing-feng1, LYU Hai-yan1, CHEN Shan-shan1, CHEN Hao1()   

  1. 1.College of Horticulture, Jilin Agricultural University, Changchun 130000
    2.Donggang District Bureau of Agriculture and Rural Affairs, Rizhao 276800
  • Received:2025-05-25 Published:2026-03-26 Online:2026-04-23

摘要:

目的 探究外源脱落酸(ABA)及其合成抑制剂NDGA对‘绿美人’薄皮甜瓜采后软化的调控机制,重点阐明ABA通过乙烯信号通路及ASR转录因子的层级调控网络,解析ABA与乙烯协同、独立调控果实软化的时空模式,为靶向保鲜技术的开发提供理论依据。 方法 以薄皮甜瓜‘绿美人’为材料,外源注射600 μmol/L ABA或50 μmol/L NDGA,测定贮藏期间果实硬度、呼吸速率、乙烯释放量及关键酶活性,结合转录组测序分析差异表达基因(DEGs),并通过qPCR验证ABA和乙烯相关基因的时序表达特征。 结果 ABA处理诱导果实提前软化,早期短暂抑制PG活性,激活β-Gal,后期显著提升PG活性、乙烯释放量及呼吸跃变峰值。NDGA有效延缓软化,维持硬度,抑制乙烯释放及PG活性高峰。转录组筛选到4 ABA vs 4 CK的4 014个DEGs和8 ABA vs 8 CK的5 161个DEGs,富集于植物激素信号转导(KO04075)、苯丙烷生物合成(KO00940)及MAPK通路(KO04016)。CmEIN/EIL/ERFCmNCED/CYP707A形成共表达模块,而CmASR1与乙烯合成基因(LOC103483612)显著正相关。qPCR证实ABA诱导CmASR1/3持续高表达、CmACS1/6CmACO3早期高表达,晚期通过CmEIN3-like1CmERF1上调CmACO3,抑制CmCYP707A2。NDGA则激活CmASR2。 结论 ABA可能通过激活ASR家族基因诱导CmEIN3CmACO基因时序性表达,协同调控乙烯合成与细胞壁代谢,而NDGA通过抑制CmCYP707A2延缓软化。揭示ABA-ASR-乙烯级联通路在薄皮甜瓜采后成熟中的重要作用,为靶向调控果实成熟提供理论依据。

关键词: 薄皮甜瓜, 脱落酸, 乙烯合成, 乙烯信号通路, 采后成熟, 果实软化, ASR基因表达, 转录

Abstract:

Objective To explore the regulatory mechanism of exogenous abscisic acid (ABA) and its synthesis inhibitor NDGA on post-harvest softening of ‘Green Beauty’ oriental melons (Cucumis melo var. Makuwa Makino), focusing on elucidation of ABA regulating network through the ethylene signaling pathway and ASR transcription factor hierarchical, analyzing the spatiotemporal model of ABA and ethylene synergistically or independently regulating fruit softening, thus providing a theoretical basis for the development of targeted preservation technology. Method The oriental melon ‘Green Beauty’ was used as the material, and exogenous injection of 600 μmol/L ABA or 50 μmol/L NDGA was conducted. The fruit hardness, respiration rate, ethylene release amount, and key enzyme activity were determined during storage. Differentially expressed genes (DEGs) were analyzed in combination with transcriptome sequencing, and the timing expression characteristics of ABA and ethylene-related genes were verified by qPCR. Result ABA treatment induced early softening of the fruit, briefly inhibited PG activity in the early stage, activated β-Gal, and significantly improved PG activity, ethylene release and respiratory jump transformation peak value in the later stage. NDGA effectively delayed softening, maintained hardness, and inhibited ethylene release and peak PG activity. The transcriptome was screened into 4 014 DEGs of 4 ABA vs 4 CK and 5 161 DEGs of 8 ABA vs 8 CK, and was enriched in phytohormone signal transduction (KO04075), styrene biosynthesis (KO00940), and MAPK pathway (KO04016). CmEIN/EIL/ERF formed a co-expression module with CmNCED/CYP707A, while CmASR1 was significantly and positively correlated with the ethylene synthesis gene (LOC103483612). qPCR confirmed that ABA induced continuous high expression of CmASR1/3, early high expression of CmACS1/6 and CmACO3, and in the late stage upregulation of CmACO3 through CmEIN3-like1 and CmERF1, inhibiting CmCYP707A2. NDGA activated CmASR2. Conclusion ABA may induce temporal expression of CmEIN3 and CmACO genes by activating ASR family genes, and coordinate the regulation of ethylene synthesis and cell wall metabolism, while NDGA delays softening by inhibiting CmCYP707A2. It reveals the important role of the ABA-ASR-ethylene cascade pathway in post-harvest maturity of oriental melons, and which may provide a theoretical basis for targeted regulation of fruit maturity.

Key words: oriental melon, abscisic acid, ethylene synthesis, ethylene signaling pathway, post-harvest ripening, fruit softening, ASR gene expression, transcription