Zhang Zengcui, Running Katherine L D, Seneviratne Sudeshi, Peters Haugrud Amanda R, Szabo-Hever Agnes, Singh Gurminder, Holušová Kateřina, Molnár István, Doležel Jaroslav, Friesen Timothy L, Faris Justin D
USDA-ARS, Cereal Crops Research Improvement Unit, Edward T. Schafer Agricultural Research Center, Fargo, ND 58102, U.S.A.
Department of Plant Sciences, North Dakota State University, Fargo, ND 58108, U.S.A.
Mol Plant Microbe Interact. 2025 Mar;38(2):315-327. doi: 10.1094/MPMI-10-24-0125-FI. Epub 2025 Apr 16.
The wheat- pathosystem has emerged as a model system for plant-necrotrophic fungal pathogen interactions. In this system, fungal necrotrophic effectors are recognized by specific host genes in an inverse gene-for-gene manner to induce programmed cell death and other host responses, which leads to disease. We previously cloned a wheat gene () encoding protein kinase and major sperm protein domains that recognizes the necrotrophic effector SnTox3. Here, we identified an homoeolog () and a paralog () that also recognize SnTox3, leading to susceptibility. DNA sequence divergence of and and differences in transcriptional expression patterns and three-dimensional protein conformation were associated with a more severe programmed cell death response conferred by compared with . Both Snn3 proteins were localized to the nucleus and cytoplasm in wheat protoplasts, suggesting that they may have acquired novel functions compared with previously characterized major sperm protein domain-containing proteins in other species. was previously shown to govern osmotic stress and salt tolerance, indicating that protein kinase-major sperm protein genes can act in plant defense responses to both biotic and abiotic stresses. Evaluation of a large collection of wheat lines showed that several alleles of each gene, including absent alleles, exist within the germplasm. Diagnostic markers were developed for the absent alleles of both genes, which will prove useful for marker-assisted selection in wheat to eliminate SnTox3 sensitivity and achieve better disease resistance. [Formula: see text] The author(s) have dedicated the work to the public domain under the Creative Commons CC0 "No Rights Reserved" license by waiving all of his or her rights to the work worldwide under copyright law, including all related and neighboring rights, to the extent allowed by law, 2025.
小麦-坏死营养型真菌病原体互作系统已成为植物与坏死营养型真菌病原体相互作用的模式系统。在该系统中,真菌坏死营养型效应子以反向基因对基因的方式被特定宿主基因识别,从而诱导程序性细胞死亡和其他宿主反应,进而导致病害。我们之前克隆了一个编码蛋白激酶和主要精子蛋白结构域的小麦基因(),该基因可识别坏死营养型效应子SnTox3。在此,我们鉴定出一个同源基因()和一个旁系同源基因(),它们也能识别SnTox3,从而导致感病。与相比,和的DNA序列差异以及转录表达模式和三维蛋白质构象的差异与更严重的程序性细胞死亡反应相关。两种Snn3蛋白都定位于小麦原生质体的细胞核和细胞质中,这表明与其他物种中先前鉴定的含主要精子蛋白结构域的蛋白质相比,它们可能获得了新功能。先前已证明可调控渗透胁迫和耐盐性,这表明蛋白激酶-主要精子蛋白基因可在植物对生物和非生物胁迫的防御反应中发挥作用。对大量小麦品系的评估表明,种质中存在每个基因的多个等位基因,包括缺失等位基因。针对这两个基因的缺失等位基因开发了诊断标记,这将有助于小麦的标记辅助选择,以消除对SnTox3的敏感性并实现更好的抗病性。[公式:见正文]作者已根据知识共享CC0“无保留权利”许可,在法律允许的范围内,放弃其在全球范围内对该作品的所有版权,包括所有相关和相邻权利,将该作品奉献给公共领域,2025年。