河南农业科学 ›› 2026, Vol. 55 ›› Issue (6): 81-91.DOI: 10.15933/j.cnki.1004-3268.2026.06.008

• 植物保护 • 上一篇    下一篇

小麦丝氨酸/苏氨酸激酶对白粉菌和植物激素的分子响应

王俊美1,刘露露1,刘凯2,李亚红1,冯超红1,石瑞杰1,韩自行1,杜习军3,徐飞1   

  1. (1.河南省农业科学院 植物保护研究所/农业农村部华北南部作物有害生物综合治理重点实验室,河南 郑州 450002;2.河南省植物保护检疫站,河南 郑州 450002;3.河南省作物分子育种研究院,河南 郑州 450002)
  • 收稿日期:2025-04-03 接受日期:2025-05-23 出版日期:2026-06-15 发布日期:2026-06-17
  • 通讯作者: 徐飞,研究员,博士,主要从事小麦病害研究。E-mail:xufei198409@163.com
  • 作者简介:王俊美,副研究员,博士,主要从事小麦病害研究。E-mail:935669594@qq.com
  • 基金资助:
    河南省小麦产业技术体系项目(HARS-22-01-G6);河南省农业科学院自主创新项目(2026ZC65);河南省重大科技专项(231100110100)

Molecular Response of Wheat Serine/Threonine Kinase to Blumeria graminis f.sp.tritici and Plant Hormones

WANG Junmei1,LIU Lulu1,LIU Kai2,LI Yahong1,FENG Chaohong1,SHI Ruijie1,HAN Zihang1,DU Xijun3,XU Fei1   

  1. (1.Institute of Plant Protection,Henan Academy of Agricultural Sciences/Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China,Ministry of Agriculture and Rural Affairs of the People’s Republic of China,Zhengzhou 450002,China;2.Henan Plant Protection and Quarantine Station,Zhengzhou 450002,China;3.Institute of Crop Molecular Breeding,Zhengzhou 450002,China)
  • Received:2025-04-03 Accepted:2025-05-23 Published:2026-06-15 Online:2026-06-17

摘要: 为阐明小麦丝氨酸/苏氨酸激酶基因(Triticum aestivum serine/threonine kinase,TaSTK)在响应布氏白粉菌(Blumeria graminis f.sp.tritici,Bgt)侵染及植物激素处理过程中的表达特征,分别从感病小麦品种豫麦13和抗病小麦品种红蚰麦中克隆TaSTK 基因,并对其编码蛋白、表达模式及亚细胞定位进行分析。结果表明,从豫麦13和红蚰麦中均获得了TaSTK基因的全长序列,2个基因序列的相似性为98%,均含有完整的开放阅读框,分别编码476个(GenBank登录号:ADP09024.1)和473个氨基酸残基(GenBank登录号:ADP09025.1)。2个TaSTK蛋白均含有典型的丝氨酸/苏氨酸激酶保守结构域。蛋白质结构分析显示,豫麦13 TaSTK蛋白在二级结构上比红蚰麦TaSTK蛋白多了一个β-折叠和一个α-螺旋,导致二者三级结构存在差异。实时定量PCR分析表明,豫麦13TaSTK基因在接种Bgt96 h后表达量显著下降;而红蚰麦与不同Bgt菌株的互作组合中,TaSTK基因表达量在接种24 h后均达到峰值,且在亲和组合(红蚰麦/BgtZZ)中的相对表达量高于非亲和组合(红蚰麦/BgtGY)。进一步利用植物激素水杨酸、茉莉酸甲酯、乙烯和脱落酸处理红蚰麦,TaSTK基因表达量在水杨酸处理6 h后达到峰值,为处理0 h的2.61倍;在茉莉酸甲酯、乙烯处理后0.5 h达到峰值,分别为处理0 h的6.16、4.81倍;在脱落酸处理0.5、24 h出现2个峰值,分别为处理0 h的7.54倍和13.29倍。瞬时表达分析显示,红蚰麦中TaSTK蛋白定位于质膜上。综上所述,TaSTK 基因参与小麦与白粉菌的互作和植物激素信号途径的应答反应。

关键词: 小麦, 小麦白粉菌, 植物激素, 丝氨酸/苏氨酸激酶, 同源克隆, 表达模式, 响应机制

Abstract: To elucidate the response characteristics of the wheat serine/threonine kinase gene(TaSTK)to Blumeria graminis f.sp.tritici(Bgt)infection and exogenous plant hormone treatments,TaSTK genes were cloned from the susceptible wheat cultivar Yumai 13 and resistant wheat cultivar Hongyoumai,respectively,followed by analyses of their encoded proteins,expression patterns and subcellular localization.The full⁃length sequences of TaSTK from Yumai 13 and Hongyoumai were obtained through homologous cloning,the similarity of the two gene sequences was 98%.Both genes contained complete open reading frames,encoding 476(GenBank accession No.ADP09024.1)and 473(GenBank accession No.ADP09025.1)amino acid residues,respectively.Both proteins possessed typical conserved domains of serine/threonine protein kinases.Protein structural analysis revealed that Yumai 13 TaSTK protein contained one additional β⁃sheet and one additional α⁃helix in its secondary structure compared with Hongyoumai TaSTK protein,resulting in different tertiary structures. Real⁃time quantitative PCR analysis indicated that the expression level of the TaSTK gene in Yumai 13 was significantly decreased at 96 h post inoculation with Bgt.By contrast,TaSTK expression in different Hongyoumai⁃Bgt interaction combinations peaked at 24 h post inoculation,and was higher in the compatible interaction(Hongyoumai/BgtZZ)than the incompatible one(Hongyoumai/BgtGY).Furthermore,when Hongyoumai was treated with plant hormones,salicylic acid(SA),methyl jasmonate(MeJA),ethylene(ETH),and abscisic acid(ABA),TaSTK expression peaked at 6 h after SA treatment,reaching 2.61⁃fold of 0 h;expression peaked at 0.5 h after MeJA and ETH treatments,reaching 6.16⁃fold and 4.81⁃fold of 0 h,respectively;and showed two peaks at 0.5 h and 24 h after ABA treatment,reaching 7.54⁃fold and 13.29⁃fold of 0 h,respectively.Transient expression analysis revealed that TaSTK protein from Hongyoumai was localized to the plasma membrane.These results demonstrate that TaSTK participates in wheat⁃Bgt interactions and responds to plant hormone signaling pathways.

Key words: Wheat, Blumeria graminis f.sp.tritici, Plant hormone, Serine/threonine kinase, Homologous cloning, Expression pattern, Response mechanism

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