Agriculture and Agri-Food Canada, Swift Current Research and Development Centre, Swift Current, Canada.
Aquatic and Crop Resource Development Centre, National Research Council Canada, Saskatoon, Canada.
PLoS One. 2018 Oct 11;13(10):e0204362. doi: 10.1371/journal.pone.0204362. eCollection 2018.
Breeding for Fusarium head blight (FHB) resistance in durum wheat is complicated by the quantitative trait expression and narrow genetic diversity of available resources. High-density mapping of the FHB resistance quantitative trait loci (QTL), evaluation of their co-localization with plant height and maturity QTL and the interaction among the identified QTL are the objectives of this study. Two doubled haploid (DH) populations, one developed from crosses between Triticum turgidum ssp. durum lines DT707 and DT696 and the other between T. turgidum ssp. durum cv. Strongfield and T. turgidum ssp. carthlicum cv. Blackbird were genotyped using the 90K Infinium iSelect chip and evaluated phenotypically at multiple field FHB nurseries over years. A moderate broad-sense heritability indicated a genotype-by-environment interaction for the expression of FHB resistance in both populations. Resistance QTL were identified for the DT707 × DT696 population on chromosomes 1B, 2B, 5A (two loci) and 7A and for the Strongfield × Blackbird population on chromosomes 1A, 2A, 2B, 3A, 6A, 6B and 7B with the QTL on chromosome 1A and those on chromosome 5A being more consistently expressed over environments. FHB resistance co-located with plant height and maturity QTL on chromosome 5A and with a maturity QTL on chromosome 7A for the DT707 × DT696 population. Resistance also co-located with plant height QTL on chromosomes 2A and 3A and with maturity QTL on chromosomes 1A and 7B for the Strongfield × Blackbird population. Additive × additive interactions were identified, for example between the two FHB resistance QTL on chromosome 5A for the DT707 × DT696 population and the FHB resistance QTL on chromosomes 1A and 7B for the Strongfield × Blackbird population. Application of the Single Nucleotide Polymorphic (SNP) markers associated with FHB resistance QTL identified in this study will accelerate combining genes from the two populations.
在硬粒小麦中培育对赤霉病(FHB)的抗性较为复杂,因为可用资源的数量性状表达和遗传多样性较窄。本研究的目的是高密度定位 FHB 抗性数量性状基因座(QTL),评估它们与株高和成熟 QTL 的共定位以及鉴定 QTL 之间的相互作用。两个双单倍体(DH)群体,一个是由 Triticum turgidum ssp. durum 品系 DT707 和 DT696 之间的杂交和另一个是 T. turgidum ssp. durum 品种 Strongfield 和 T. turgidum ssp. carthlicum 品种 Blackbird 之间的杂交产生的,使用 90K Infinium iSelect 芯片进行基因型分析,并在多年的多个田间赤霉病苗圃中进行表型评估。两个群体的 FHB 抗性均表现出中度广泛遗传力,表明存在基因型与环境的互作。在 DT707 × DT696 群体中,在染色体 1B、2B、5A(两个位点)和 7A 上鉴定到 FHB 抗性 QTL,在 Strongfield × Blackbird 群体中,在染色体 1A、2A、2B、3A、6A、6B 和 7B 上鉴定到 FHB 抗性 QTL,其中染色体 1A 和 5A 上的 QTL在多个环境中表达更为一致。在 DT707 × DT696 群体中,FHB 抗性与染色体 5A 上的株高和成熟 QTL 以及 7A 上的成熟 QTL 共定位。在 Strongfield × Blackbird 群体中,FHB 抗性与染色体 2A 和 3A 上的株高 QTL 以及染色体 1A 和 7B 上的成熟 QTL 共定位。鉴定到了加性×加性互作,例如在 DT707 × DT696 群体中 5A 上的两个 FHB 抗性 QTL 与 Strongfield × Blackbird 群体中 1A 和 7B 上的 FHB 抗性 QTL 之间。应用本研究中鉴定到的与 FHB 抗性 QTL 相关的单核苷酸多态性(SNP)标记将加速来自两个群体的基因的组合。