Dissecting the genetic basis of resistance to Soil-borne cereal mosaic virus (SBCMV) in durum wheat by bi-parental mapping and GWAS.

IF 4.4 1区 农林科学 Q1 AGRONOMY
Martina Bruschi, Matteo Bozzoli, Claudio Ratti, Giuseppe Sciara, Ellen Goudemand, Pierre Devaux, Danara Ormanbekova, Cristian Forestan, Simona Corneti, Sandra Stefanelli, Sara Castelletti, Elena Fusari, Jad B Novi, Elisabetta Frascaroli, Silvio Salvi, Dragan Perovic, Agata Gadaleta, Concepcion Rubies-Autonell, Maria Corinna Sanguineti, Roberto Tuberosa, Marco Maccaferri
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Abstract

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.

Abstract Image

通过双亲图谱和基因组测序分析,剖析硬粒小麦对土传谷物花叶病毒(SBCMV)抗性的遗传基础。
土传谷物花叶病毒(SBCMV)是小麦花叶病的病原体,是一种对整个欧洲的小麦生产构成挑战的呋喃病毒。与面包小麦不同,硬粒小麦的易感性更强,产量损失也更大,因此抗性来源的鉴定和遗传特性分析是硬粒小麦遗传学和育种的主要目标。在面包小麦中,对 SBCMV 具有高水平抗性的 Sbm1 基因座被映射到 5DL 染色体臂上(Bass in Genome 49:1140-1148, 2006)。这就排除了将 Sbm1 直接用于硬粒小麦改良的可能性。在硬质小麦中只绘制了一个主要的 QTL,即 QSbm.ubo-2B,位于 2BS 染色体区域,与 Sbm2 重合,据报道,面包小麦中已经知道 Sbm2(Bayles,载于 HGCA 项目报告,2007 年)。因此,QSbm.ubo-2B = Sbm2 被认为是在受 SBCMV 影响地区种植硬质小麦的支柱。在此,我们利用 Infinium 90 K SNP 阵列和高通量 KASP® 报告了基于双亲图谱和 GWAS 的 Sbm2 精细图谱。精细图谱指出了一个3.2 Mb的关键单倍区块,该单倍区块由成功转换为高通量KASP®标记的SNPs连接而成,编码为KUBO。结合 KUBO-27、wPt-2106-ASO/HRM、KUBO-29 和 KUBO-1 可以明确追踪 Sbm2-抗性单倍型。该区间包含 52 个高置信度基因和 41 个低置信度基因,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 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效率以及最终与品种特征描述和选择相关的决策过程提供了一个有价值的案例研究。
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来源期刊
CiteScore
9.60
自引率
7.40%
发文量
241
审稿时长
2.3 months
期刊介绍: Theoretical and Applied Genetics publishes original research and review articles in all key areas of modern plant genetics, plant genomics and plant biotechnology. All work needs to have a clear genetic component and significant impact on plant breeding. Theoretical considerations are only accepted in combination with new experimental data and/or if they indicate a relevant application in plant genetics or breeding. Emphasizing the practical, the journal focuses on research into leading crop plants and articles presenting innovative approaches.
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