Ruan Yuefeng, Yu Bianyun, Knox Ron E, Singh Asheesh K, DePauw Ron, Cuthbert Richard, Zhang Wentao, Piche Isabelle, Gao Peng, Sharpe Andrew, Fobert Pierre
Swift Current Research and Development Centre, Agriculture and Agri-Food Canada, Swift Current, SK, Canada.
Aquatic and Crop Resource Development, National Research Council Canada, Saskatoon, SK, Canada.
Front Plant Sci. 2020 Mar 4;11:170. doi: 10.3389/fpls.2020.00170. eCollection 2020.
Gluten strength is one of the factors that determine the end-use quality of durum wheat and is an important breeding target for this crop. To characterize the quantitative trait loci (QTL) controlling gluten strength in Canadian durum wheat cultivars, a population of 162 doubled haploid (DH) lines segregating for gluten strength and derived from cv. Pelissier × cv. Strongfield was used in this study. The DH lines, parents, and controls were grown in 3 years and two seeding dates in each year and gluten strength of grain samples was measured by sodium dodecyl sulfate (SDS)-sedimentation volume (SV). With a genetic map created by genotyping the DH lines using the Illumina Infinium iSelect Wheat 90K SNP (single nucleotide polymorphism) chip, QTL contributing to gluten strength were detected on chromosome 1A, 1B, 2B, and 3A. Two major and stable QTL detected on chromosome 1A () and 1B () explaining 13.7-18.7% and 25.4-40.1% of the gluten strength variability respectively were consistently detected over 3 years, with the trait increasing alleles derived from Strongfield. Putative candidate genes underlying the major QTL were identified. Two novel minor QTL ( and ) with the trait increasing allele derived from Pelissier were mapped on chromosome 3A explaining up to 8.9% of the phenotypic variance; another three minor QTL (, , and ) located on chromosome 2B explained up to 8.7% of the phenotypic variance with the trait increasing allele derived from Pelissier. is a new QTL and has not been reported in the literature. Multi-environment analysis revealed genetic (QTL) × environment interaction due to the difference of effect in magnitude rather than the direction of the QTL. Eleven pairs of digenic epistatic QTL were identified, with an epistatic effect between the two major QTL of and detected in four out of six environments. The peak SNPs and SNPs flanking the QTL interval of and were converted to Kompetitive Allele Specific PCR (KASP) markers, which can be deployed in marker-assisted breeding to increase the efficiency and accuracy of phenotypic selection for gluten strength in durum wheat. The QTL that were expressed consistently across environments are of great importance to maintain the gluten strength of Canadian durum wheat to current market standards during the genetic improvement.
面筋强度是决定硬粒小麦最终使用品质的因素之一,也是该作物的一个重要育种目标。为了鉴定控制加拿大硬粒小麦品种面筋强度的数量性状位点(QTL),本研究使用了一个由162个双单倍体(DH)株系组成的群体,这些株系由Pelissier品种×Strongfield品种杂交产生,在面筋强度上存在分离。DH株系、亲本和对照在3年中种植,每年有两个播种日期,通过十二烷基硫酸钠(SDS)沉降体积(SV)测量谷物样品的面筋强度。利用Illumina Infinium iSelect小麦90K单核苷酸多态性(SNP)芯片对DH株系进行基因分型构建遗传图谱,在1A、1B、2B和3A染色体上检测到了对面筋强度有贡献的QTL。在1A染色体()和1B染色体()上检测到的两个主要且稳定的QTL,分别解释了面筋强度变异的13.7 - 18.7%和25.4 - 40.1%,在3年中均被一致检测到,增加性状的等位基因来自Strongfield。鉴定了主要QTL潜在的候选基因。在3A染色体上定位了两个新的小QTL(和),增加性状的等位基因来自Pelissier,解释了高达8.9%的表型变异;位于2B染色体上的另外三个小QTL(、和),增加性状的等位基因来自Pelissier,解释了高达8.7%的表型变异。是一个新的QTL,尚未在文献中报道。多环境分析揭示了由于QTL效应大小而非方向的差异导致的遗传(QTL)×环境互作。鉴定出11对双基因上位性QTL,在六个环境中的四个环境中检测到了和这两个主要QTL之间的上位性效应。将和的QTL区间侧翼的峰值SNP转换为竞争性等位基因特异性PCR(KASP)标记,可用于标记辅助育种,以提高硬粒小麦面筋强度表型选择的效率和准确性。在不同环境中一致表达的QTL对于在遗传改良过程中将加拿大硬粒小麦的面筋强度维持在当前市场标准非常重要。