CaWRKY27通过调控CaPR1和CaPR1L的表达介导辣椒对青枯菌的免疫OA
CaWRKY27 Mediates Pepper Immunity to Ralstonia solanacearum by Regulating CaPR1 and CaPR1L Expression
植物特异性转录因子 WRKY 在调控水杨酸(salicylic acid,SA)介导的免疫中发挥着重要作用,CaWRKY27 是 CaWRKYⅡe 亚家族成员,调控辣椒(Capsicum annuum L.)对青枯病的抗性.为了进一步解析 CaWRKY27 在辣椒抗青枯病中的作用机制,共鉴定出辣椒基因组中的 5 个 CaWRKYⅡe 亚家族成员.系统进化树和氨基酸序列比对分析显示,CaWRKY27 与番茄 SlWRKY79、拟南芥 AtWRKY65同源性较高.实时荧光定量 PCR(RT-qPCR)分析表明,在接种青枯菌 24 和 48 h 后,CaWRKY27 沉默株系中病程相关基因 CaPR1 和 CaPR1L 的表达量显著低于对照株系.双荧光素报告实验和凝胶阻滞实验表明,CaWRKY27 可直接与 CaPR1 和 CaPR1L 的启动子中的 W-box 元件结合并激活其表达.上述结果表明,辣椒CaWRKY27通过直接调控SA信号途径相关基因CaPR1和CaPR1L的表达从而正调控辣椒对青枯病的抗性.
The WRKY transcription factors,which are specific to plants,play a crucial role in regulating salicylic acid(SA)-mediated immune response.CaWRKY27,a member of the CaWRKYⅡe subfamily,is implicated in modulating the resistance of pepper plants to bacterial wilt.To further elucidate the mechanism of action of CaWRKY27 gene in pepper's resistance to bacterial wilt,five members of the CaWRKYⅡe subfamily were identified within the pepper genome.Phylogenetic analysis and multiple amino acid sequence alignment revealed that CaWRKY27 exhibits a high degree of homology with SlWRKY79 from tomato and AtWRKY65 from Arabidopsis.Real-time quantitative PCR(RT-qPCR)analysis demonstrated that the expression levels of the pathogenesis-related genes CaPR1 and CaPR1L were significantly reduced in pTRV2-CaWRKY27(CaWRKY27 silencing)plants compared to at both 24 and 48 hours post-inoculation with Ralstonia solanacearum in pepper.Furthermore,both dual-luciferase reporter(DLR)assays and electrophoretic mobility shift assays(EMSA)revealed that CaWRKY27 can directly bind to the W-box in the promoters of the CaPR1 and CaPR1L genes,thereby activating their expression.These findings indicate that CaWRKY27 plays a crucial role in the resistance to bacterial wilt by directly regulating the expression of SA signaling pathway-related genes CaPR1 and CaPR1L in pepper.
折建局;田雅珊;陈风;党峰峰
延安大学生命科学学院,陕西省黄土高原资源植物研究与利用重点实验室,陕西 延安 716000延安大学生命科学学院,陕西省黄土高原资源植物研究与利用重点实验室,陕西 延安 716000延安大学生命科学学院,陕西省黄土高原资源植物研究与利用重点实验室,陕西 延安 716000延安大学生命科学学院,陕西省黄土高原资源植物研究与利用重点实验室,陕西 延安 716000
农业科技
辣椒CaWRKY27转录因子青枯病病程相关基因W-box水杨酸(SA)信号途径
pepperCaWRKY27transcription factorbacterial wiltpathogenesis-related genesW-boxSA signaling pathway
《园艺学报》 2026 (3)
831-844,14
国家自然科学基金项目(32360763)延安市重点项目(2023-CYL-160)延安大学博士科研启动项目(YAU202313800)
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