Running Katherine L D, Acharya Krishna, Roth Tiana M, Singh Gurminder, Szabo-Hever Agnes, Peters Haugrud Amanda R, Fiedler Jason D, Friesen Timothy L, Faris Justin D
Department of Plant Sciences, North Dakota State University, Fargo, ND, USA.
Cereal Crops Improvement Research Unit, Edward T. Schafer Agricultural Research Center, USDA-Agricultural Research Service, Fargo, ND, USA.
Theor Appl Genet. 2025 Jun 28;138(7):164. doi: 10.1007/s00122-025-04952-6.
The wheat gene Tsn1 confers susceptibility to tan spot, septoria nodorum blotch, and spot blotch. The markers developed here may be immediately deployed in breeding programs to eliminate Tsn1. The wheat Tsn1 gene recognizes the necrotrophic effector ToxA, which is produced by three different necrotrophic fungal pathogens. A compatible Tsn1-ToxA interaction leads to host-induced responses that result in the development of disease. Therefore, marker-assisted elimination of functional Tsn1 alleles is an effective strategy for the development of disease resistant varieties. To develop such markers, available wheat genome assemblies were used to compare gene and transposable element content in lines with and without Tsn1 (Tsn1- and Tsn1 +), revealing two conserved haplotypes. Because Tsn1 is almost always absent in insensitive lines, Kompetitive allele-specific PCR (KASP) markers were designed in flanking syntenic regions of Tsn1- and Tsn1 + assemblies. The KASP markers were validated in more than 1,500 diverse lines. The markers correctly predicted a ToxA-insensitive phenotype in 99.33-100% of the lines, but they were less effective at predicting a ToxA-sensitive phenotype (89.50-94.55%) due to 60 insensitive lines with sensitive marker alleles. Sequence analysis of Tsn1 from these lines revealed that some were not transcribed and others contained point mutations. However, some carried and expressed the dominant Tsn1 allele, and subsequent analysis of two such lines revealed a second locus controlling ToxA sensitivity on chromosome 2B, termed Tsn1-B2. Genetic mapping of Tsn1-B2 in a biparental durum population defined the locus to a 4.8 cM region corresponding to 8.6 Mb in Svevo Rel 2.0. The markers presented here could be used for reliable and robust marker-assisted elimination of Tsn1 in a high-throughput manner, furthering the development of wheat genetically resistant to multiple pathogens.
小麦基因Tsn1会使植株对黄斑病、颖枯病和斑点叶枯病易感。本文开发的标记可立即应用于育种计划以去除Tsn1。小麦Tsn1基因可识别由三种不同的坏死营养型真菌病原体产生的坏死营养型效应子ToxA。Tsn1与ToxA的相容性相互作用会引发宿主诱导的反应,从而导致病害的发展。因此,通过标记辅助消除功能性Tsn1等位基因是培育抗病品种的有效策略。为开发此类标记,利用现有的小麦基因组组装序列来比较有和没有Tsn1(Tsn1 - 和Tsn1 +)的品系中的基因和转座元件含量,揭示了两种保守单倍型。由于Tsn1在不敏感品系中几乎总是不存在,因此在Tsn1 - 和Tsn1 +组装序列的侧翼同线区域设计了竞争性等位基因特异性PCR(KASP)标记。这些KASP标记在1500多个不同品系中得到了验证。这些标记在99.33% - 100%的品系中正确预测了对ToxA不敏感的表型,但由于60个具有敏感标记等位基因的不敏感品系,它们在预测对ToxA敏感的表型时效果较差(89.50% - 94.55%)。对这些品系中Tsn1的序列分析表明,有些品系不转录,有些品系含有点突变。然而,有些品系携带并表达显性Tsn1等位基因,随后对其中两个品系的分析揭示了2B染色体上另一个控制对ToxA敏感性的位点,称为Tsn1 - B2。在一个双亲硬粒小麦群体中对Tsn1 - B2进行遗传定位,将该位点定位到一个4.8厘摩的区域,对应于 Svevo Rel 2.0中的8.6兆碱基。本文介绍的标记可用于以高通量方式可靠且有力地通过标记辅助消除Tsn1,推动对多种病原体具有遗传抗性的小麦的培育。