Department of Agricultural and Food Sciences (DISTAL), Alma Mater Studiorum - Università di Bologna, 40127, Bologna, Italy.
S.A.S. Florimond-Desprez Veuve and Fils, BP41, 59242, Cappelle-en-Pévèle, France.
Theor Appl Genet. 2024 Sep 2;137(9):213. doi: 10.1007/s00122-024-04709-7.
Soil-borne cereal mosaic virus (SBCMV), the causative agent of wheat mosaic, is a Furovirus challenging wheat production all over Europe. Differently from bread wheat, durum wheat shows greater susceptibility and stronger yield penalties, so identification and genetic characterization of resistance sources are major targets for durum genetics and breeding. The Sbm1 locus providing high level of resistance to SBCMV was mapped in bread wheat to the 5DL chromosome arm (Bass in Genome 49:1140-1148, 2006). This excluded the direct use of Sbm1 for durum wheat improvement. Only one major QTL has been mapped in durum wheat, namely QSbm.ubo-2B, on the 2BS chromosome region coincident with Sbm2, already known in bread wheat as reported (Bayles in HGCA Project Report, 2007). Therefore, QSbm.ubo-2B = Sbm2 is considered a pillar for growing durum in SBCMV-affected areas. Herein, we report the fine mapping of Sbm2 based on bi-parental mapping and GWAS, using the Infinium 90 K SNP array and high-throughput KASP®. Fine mapping pointed out a critical haploblock of 3.2 Mb defined by concatenated SNPs successfully converted to high-throughput KASP® markers coded as KUBO. The combination of KUBO-27, wPt-2106-ASO/HRM, KUBO-29, and KUBO-1 allows unequivocal tracing of the Sbm2-resistant haplotype. The interval harbors 52 high- and 41 low-confidence genes, encoding 17 cytochrome p450, three receptor kinases, two defensins, and three NBS-LRR genes. These results pave the way for Sbm2 positional cloning. Importantly, the development of Sbm2 haplotype tagging KASP® provides a valuable case study for improving efficacy of the European variety testing system and, ultimately, the decision-making process related to varietal characterization and choice.
土传小麦花叶病毒(SBCMV)是引起小麦花叶病的病原体,它是一种在整个欧洲对小麦生产构成挑战的斐诺病毒。与面包小麦不同,杜伦小麦表现出更高的易感性和更强的产量损失,因此,鉴定和遗传特征抗性来源是杜伦小麦遗传和育种的主要目标。在面包小麦中,SBCMV 高水平抗性的 Sbm1 基因座被定位在 5DL 染色体臂上(Bass 在 Genome 49:1140-1148, 2006 年)。这排除了直接将 Sbm1 用于杜伦小麦改良的可能性。在杜伦小麦中,只有一个主要的 QTL 被定位在 2BS 染色体区域,即 QSbm.ubo-2B,与面包小麦中的 Sbm2 重合,如报告所述(Bayles 在 HGCA 项目报告中,2007 年)。因此,QSbm.ubo-2B=Sbm2 被认为是在 SBCMV 疫区种植杜伦小麦的重要支柱。在此,我们基于双亲作图和 GWAS 报告了 Sbm2 的精细作图,使用 Infinium 90K SNP 阵列和高通量 KASP®。精细作图指出了一个由 3.2 Mb 串联 SNP 定义的关键单倍型块,这些 SNP 成功转化为高通量 KASP®标记,编码为 KUBO。KUBO-27、wPt-2106-ASO/HRM、KUBO-29 和 KUBO-1 的组合允许明确追踪 Sbm2 抗性单倍型。该区间包含 52 个高可信度和 41 个低可信度基因,编码 17 个细胞色素 P450、3 个受体激酶、2 个防御素和 3 个 NBS-LRR 基因。这些结果为 Sbm2 的定位克隆铺平了道路。重要的是,Sbm2 单倍型标记 KASP®的开发为提高欧洲品种测试系统的功效提供了一个有价值的案例研究,最终为品种特征描述和选择的决策过程提供了支持。