中国农业科学 ›› 2026, Vol. 59 ›› Issue (12): 2712-2725.doi: 10.3864/j.issn.0578-1752.2026.12.013

• 园艺 • 上一篇    下一篇

枇杷日灼响应因子EjWRKY15互作蛋白的筛选及其调控网络解析

李晓颖1(), 陈鑫鹏2, 葛航1, 陈俊伟1, 王晨2, 徐红霞1()   

  1. 1 浙江省农业科学院园艺研究所, 杭州 310021
    2 南京农业大学园艺学院, 南京 210095
  • 收稿日期:2026-01-09 接受日期:2026-04-07 出版日期:2026-06-16 发布日期:2026-06-16
  • 通信作者:
    徐红霞,E-mail:
  • 联系方式: 李晓颖,E-mail:lixy@zaas.ac.cn。
  • 基金资助:
    国家青年科学基金(31601734); 浙江省“十四五”果品新品种选育专项-枇杷新品种选育(2021C02066-3)

Screening of Interacting Proteins for the Loquat Sunburn-Responsive Factor EjWRKY15 and Analysis of Its Regulatory Network

LI XiaoYing1(), CHEN XinPeng2, GE Hang1, CHEN JunWei1, WANG Chen2, XU HongXia1()   

  1. 1 Institute of Horticulture, Zhejiang Academy of Agricultural Sciences, Hangzhou 310021
    2 College of Horticulture, Nanjing Agricultural University, Nanjing 210095
  • Received:2026-01-09 Accepted:2026-04-07 Published:2026-06-16 Online:2026-06-16

摘要:

【目的】枇杷(Eriobotrya japonica)是我国南方重要的经济果树,其果实成熟期正值高温强光季节,极易发生日灼伤害,表现为果皮褐变、组织坏死及风味劣变,严重削弱果实商品率与经济价值。WRKY转录因子作为植物特有的逆境响应调控因子,在高温、干旱等非生物胁迫中发挥关键作用,解析EjWRKY15在日灼胁迫中的功能及作用机制,为揭示枇杷日灼响应的调控通路和创制抗日灼新种质提供理论依据与候选基因资源。【方法】以枇杷果实为材料,利用SMART技术构建日灼胁迫诱导的枇杷果实酵母双杂交cDNA文库,通过涂布筛选与序列回测鉴定文库的库容、滴度和重组率。以EjWRKY15为诱饵蛋白,通过酵母双杂交系统(Y2H)从文库中筛选其潜在的互作蛋白。利用NCBI、Swiss-Prot等数据库对筛选到的互作蛋白进行功能注释,并重点关注高温及逆境相关蛋白。采用酵母双杂交点对点试验(Y2H)和双分子荧光互补技术(BiFC)分别从体外和体内水平验证EjWRKY15与候选蛋白EjLHP1.2(like heterochromatin protein 1)的物理互作真实性。基于转录组数据和关联分析,构建以EjWRKY15为核心节点的枇杷日灼应答分子互作网络。【结果】成功构建了库容量大、重组率高的枇杷果实cDNA文库。通过诱饵载体自激活检测排除背景干扰后,酵母双杂交筛选获得12个与EjWRKY15互作的候选蛋白,功能涉及表观遗传调控、胁迫信号转导和物质代谢等。其中,鉴定到一个与高温响应密切相关的基因EjLHP1.2。点对点验证与BiFC试验证实EjWRKY15与EjLHP1.2在体内和体外均存在互作。表达分析显示,在日灼胁迫下,EjWRKY15及其12个互作候选蛋白基因均呈现显著的差异表达模式。基于上述互作关系和表达关联,初步构建了EjWRKY15介导的日灼应答网络,表明EjWRKY15可能通过招募EjLHP1.2等因子共同调节下游热响应基因的表达。【结论】阐明了核心转录因子EjWRKY15通过与表观遗传调节因子EjLHP1.2发生蛋白互作,进而精准调控下游响应网络并介导枇杷果实日灼应答的分子机制,揭示了枇杷在遭遇高温强光胁迫时,通过“转录因子-染色质重塑蛋白”协同模式进行逆境调控的新路径。

关键词: 枇杷, 日灼, EjWRKY15, EjLHP1.2, 酵母双杂交, 双分子荧光互补

Abstract:

【Objective】Loquat (Eriobotrya japonica), a significant economic fruit tree in southern China, is highly susceptible to sunburn injury during its ripening stage, which typically coincides with periods of high temperature and intense light. Sunburn manifests as fruit peel browning, tissue necrosis, and flavor deterioration, severely undermining both the marketability and economic value of the fruit. WRKY transcription factors, as plant-specific regulators of stress responses, play pivotal roles in abiotic stresses such as high temperature and drought. This study aims to analyze the function and regulatory mechanism of EjWRKY15 under sunburn stress, providing a theoretical foundation and candidate gene resources for elucidating the sunburn response pathways in loquat and developing sunburn-resistant germplasms.【Method】Centering on the transcription factor EjWRKY15, its interacting proteins were screened and validated to systematically characterize its expression profiles and molecular interaction networks under sunburn stress. A sunburn -induced yeast two-hybrid (Y2H) cDNA library of loquat fruit was constructed using SMART technology. The library capacity, titer, and recombination rate were evaluated through plating selection and sequence analysis. Using EjWRKY15 as the bait protein, potential interactors were screened from the library via the Y2H system. Functional annotation of the screened proteins was performed using NCBI, Swiss-Prot, and other databases, focusing on factors related to heat and stress responses. The physical interaction between EjWRKY15 and the candidate protein EjLHP1.2 (Like Heterochromatin Protein 1) was validated both in vitro and in vivo through one-on-one Y2H assays and bimolecular fluorescence complementation (BiFC). Based on transcriptome data and correlation analysis, a molecular interaction network for loquat sunburn response was constructed with EjWRKY15 as the core node.【Result】A high-quality cDNA library of loquat fruit with a large capacity and high recombination rate was successfully constructed. After excluding background interference via bait self-activation assays, 12 candidate proteins interacting with EjWRKY15 were obtained, with functions involving epigenetic regulation, stress signaling, and substance metabolism. Notably, EjLHP1.2, which is closely associated with sunburn response, was identified as a key interactor. One-on-one Y2H and BiFC assays confirmed that EjWRKY15 and EjLHP1.2 interact physically both in vivo and in vitro. Expression analysis revealed that EjWRKY15 and its 12 candidate interactor genes exhibited significant differential expression patterns under sunburn stress. Based on the interaction data and expression correlations, an EjWRKY15-mediated sunburn response network was preliminarily established. The network suggests that EjWRKY15 may precisely regulate downstream heat-responsive genes by recruiting EjLHP1.2 and other factors.【Conclusion】This study identified the interacting proteins of EjWRKY15 and revealed its expression patterns and molecular interaction network in the sunburn response of loquat. The results elucidate the molecular mechanism by which the core transcription factor EjWRKY15 mediates the sunburn response of loquat fruit through its protein interaction with the epigenetic regulator EjLHP1.2 and the precise modulation of the associated interaction network. These findings reveal a novel stress-regulatory pathway involving the synergetic mode of transcription factor-chromatin remodeling protein in loquat under high temperature and strong light, providing critical theoretical support and gene resources for the molecular breeding of sunburn-resistant loquat varieties.

Key words: loquat, sunburn, EjWRKY15, EjLHP1.2, yeast two-hybrid, BiFC