生物技术通报 ›› 2026, Vol. 42 ›› Issue (8): 123-132.doi: 10.13560/j.cnki.biotech.bull.1985.2025-1109

• 研究报告 • 上一篇    

小麦HD-Zip基因家族的鉴定及对禾谷镰刀菌的响应

吕正1,2, 连如赢2, 刘怡德2, 刘易科2, 宁强2(), 王书平1()   

  1. 1.长江大学农学院 农业农村部长江中游作物绿色高效生产重点实验室(部省共建),荆州 434025
    2.湖北省农业科学院粮食作物研究所 农业农村部作物分子育种重点实验室 粮食作物种质创新与遗传改良湖北省重点实验室,武汉 430064
  • 收稿日期:2025-10-16 出版日期:2026-08-26 发布日期:2026-08-17
  • 通讯作者: 宁强ningqiang_404@163.com
    王书平wangshuping2003@126.com
  • 基金资助:
    国家自然科学基金项目(32272170);襄阳市科技计划(2023)

Wheat HD-Zip Gene Family: Identification and Response to Fusarium graminearum

LYU Zheng1,2, LIAN Ru-ying2, LIU Yi-de2, LIU Yi-ke2, NING Qiang2(), WANG Shu-ping1()   

  1. 1.College of Agronomy, Yangtze University, Key Laboratory of Sustainable Crop Production in the Middle Reaches of the Yangtze River (Co-Construction by Ministry and Province), Ministry of Agriculture and Rural Affairs, Jingzhou 434025
    2.Institute of Food Crops, Hubei Academy of Agricultural Sciences, Key Laboratory of Crop Molecular Breeding, Ministry of Agriculture and Rural Affairs, Hubei Key Laboratory of Food Crop Germplasm and Genetic Improvement, Wuhan 430064
  • Received:2025-10-16 Published:2026-08-26 Online:2026-08-17

摘要:

目的 系统鉴定小麦同源异型结构域-亮氨酸拉链(HD-Zip)基因家族成员,分析其在不同组织和发育时期的表达特征,以及在响应禾谷镰刀菌中的作用,为解析小麦HD-Zip基因家族功能提供理论基础。 方法 以拟南芥HD-Zip蛋白序列为参考,利用小麦基因组数据库筛选家族成员,并进行蛋白质理化性质分析、系统进化树构建、染色体定位及基因结构解析;进一步结合转录组和RT-qPCR数据,分析其在不同组织及禾谷镰刀菌侵染下的表达模式。 结果 共鉴定85个小麦HD-Zip基因,其编码蛋白均为亲水蛋白,且均被预测为不稳定蛋白。亚细胞定位预测表明,HD-Zip基因主要分布于细胞核和叶绿体。系统进化树和结构分析显示,HD-Zip基因分为4个进化分支,同一分支基因在基因结构和保守基序上具有高度一致性,且非均匀地分布于22条染色体。启动子区域分析表明,HD-Zip基因普遍含有与脱落酸(ABA)、赤霉素(GA)、茉莉酸甲酯(MeJA)、水杨酸(SA)和生长素(IAA)相关的顺式作用元件,以及逆境响应、根特异性和胚乳调控等功能元件。65个基因在穗、叶、芽、根和籽粒中均有表达。特别是在禾谷镰刀菌侵染条件下,TaHDZ1.1-6BTaHDZ1.1-5ATaHDZ1.1-5BTaHDZ1.1-5D等基因在不同处理时间点均显著上调,且在抗病和感病品种中的诱导表达模式一致。 结论 小麦HD-Zip基因家族在进化过程中表现出高度保守性,可能通过差异表达参与组织器官的发育调控及生物与非生物逆境响应。其中,TaHDZ1.1-6BTaHDZ1.1-5ATaHDZ1.1-5B等基因可能在小麦赤霉病防御反应中发挥关键作用。

关键词: 小麦, HD-Zip基因家族, 表达分析, 胁迫响应, 禾谷镰刀菌响应

Abstract:

Objective To systematically identify the members of the wheat homeodomain-leucine zipper (HD-Zip) gene family, analyze their expression patterns across different tissues and developmental stages, and investigate their roles in response to Fusarium graminearum, thereby providing a theoretical basis for functional characterization of the wheat HD-Zip gene family. Method Using Arabidopsis HD-Zip protein sequences as queries, the members of the wheat HD-Zip gene family were identified from the wheat genome database. Protein physicochemical properties, phylogenetic tree construction, chromosome mapping and gene structure analysis were analyzed. Furthermore, transcriptome data and RT-qPCR were employed to assess the expression profiles of these genes in various tissues and under F. graminearum infection. Result A total of 85 wheat HD-Zip genes were identified, all of which encoded hydrophilic proteins, and were predicted to be unstable. Subcellular localization indicated that most HD-Zip proteins were localized in the nucleus and chloroplast. Phylogenetic and structural analyses revealed that these genes were grouped into four evolutionary clades, with members of the same clade showing high similarity in gene structure and conserved motifs, and were unevenly distributed across 22 chromosomes. Promoter analysis indicated the widespread presence of cis-acting elements associated with abscisic acid (ABA), gibberellin (GA), methyl jasmonate (MeJA), salicylic acid (SA), and auxin (IAA), as well as elements involved in stress responses, root specificity, and endosperm regulation. Expression analysis showed that 65 genes were expressed in the spikes, leaves, shoots, roots, and grains. Notably, under F. graminearum infection, genes such as TaHDZ1.1-6B, TaHDZ1.1-5A, TaHDZ1.1-5B, and TaHDZ1.1-5D were significantly upregulated at multiple time points, exhibiting consistent inducible expression patterns in both resistant and susceptible cultivars. Conclusion The wheat HD-Zip gene family presents strong evolutionary conservation and is likely involved in both organ development and responses to biotic and abiotic stresses through differential expression. Among them, TaHDZ1.1-6B, TaHDZ1.1-5A and TaHDZ1.1-5B may play crucial roles in wheat defense against F. graminearum.

Key words: wheat, HD-Zip gene family, expression analysis, stress response, Fusarium graminearum response