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High Density Mapping of Quantitative Trait Loci Conferring Gluten Strength in Canadian Durum Wheat

机译:加拿大杜兰麦小麦赋予筋筋力量的定量特质基因座的高密度映射

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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 ( QGlu.spa-1A ) and 1B ( QGlu.spa-1B.1 ) 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 ( QGlu.spa-3A.1 and QGlu.spa-3A.2 ) 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 ( QGlu.spa-2B.1 , QGlu.spa-2B.2 , and QGlu.spa-2B.3 ) located on chromosome 2B explained up to 8.7% of the phenotypic variance with the trait increasing allele derived from Pelissier. QGlu.spa-2B.1 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 QGlu.spa-1A and QGlu.spa-1B.1 detected in four out of six environments. The peak SNPs and SNPs flanking the QTL interval of QGlu.spa-1A and QGlu.spa-1B.1 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.
机译:麸质强度是确定杜兰姆小麦的最终使用质量的因素之一,是这种作物的重要育种目标。为了表征控制加拿大杜兰麦小麦品种筋强化的定量特质基因座(QTL),162个双倍单倍体(DH)分离的群体用于麸质强度和衍生自CV。 pelissier×cv。在这项研究中使用了强菲尔德。在3年内生长DH线,父母和对照,每年的两次播种日期和谷粒样品的筋强度由十二烷基硫酸钠(SDS) - 索己烷体积(SV)测量。通过使用Illumina Infinium Inelect小麦90K(单核苷酸多态性)芯片基因分型的基因分型产生的遗传图,在染色体1A,1B,2B和3A上检测到促进筋强度的QTL。在染色体1A(QGLU.SPA-1A)和1B(QGLU.SPA-1B.1)上检测到两种主要和稳定的QTL(QGLU.SPA-1B.1)分别持续检测到3年来的13.7-18.7%和25.4-40.1%,持续检测到3年,随着来自强方的特质增加等位基因。鉴定了主要QTL下面的推定候选基因。两种新的次要QTL(QGLU.SPA-3A.1和QGLU.SPA-3A.2)均在染色体3A上映射到染色体的表型差异的8.9%;位于染色体2B上的另外三个小QTL(QGLU.SPA-2B.1,QGLU.SPA-2B.2和QGLU.SPA-2B.3)解释了高达8.7%的表型方差,其具有来自的性状增加的等位基因pelissier。 QGLU.SPA-2B.1是一个新的QTL,尚未在文献中报告。多环境分析显示遗传(QTL)×环境相互作用由于效果的差异而不是QTL的方向。鉴定了十一对的数字电子QTL,在六个环境中四个QGLU.SPA-1A和QGLU.SPA-1B.1中的两个主要QTL之间的认证效果。将QGLu.SPA-1A和QGLU.SPA-1B.1的QTL间隔侧翼的峰值SNP和SNP转化为KMPTIVE等位基因特异性PCR(KASP)标记,其可以部署在标记辅助的繁殖中,以提高效率和准确性杜兰姆小麦面筋强度的表型选择。在环境中一致表达的QTL非常重视在遗传改进期间维持加拿大杜兰姆小麦的麸质实力到当前的市场标准。

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