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Genome-wide association mapping for eyespot disease in US Pacific Northwest winter wheat

机译:全基因组关联映射在美国太平洋西北地区冬小麦的眼斑病

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摘要

Eyespot, caused by the soil-borne necrotrophic fungi Oculimacula yallundae and O. acuformis, is a disease of major economic significance for wheat, barley and rye. Pacific Northwest (PNW) winter wheat (Triticum aestivum L.) grown in areas of high rainfall and moderate winters is most vulnerable to infection. The objective of this research was to identify novel genomic regions associated with eyespot resistance in winter wheat adapted to the PNW. Two winter wheat panels of 469 and 399 lines were compiled for one of the first genome-wide association studies (GWAS) of eyespot resistance in US winter wheat germplasm. These panels were genotyped with the Infinium 9K and 90K iSelect SNP arrays. Both panels were phenotyped for disease resistance in a two-year field study and in replicated growth chamber trials. Growth chamber trials were used to evaluate the genetic resistance of O. acuformis and O. yallundae species separately. Best linear unbiased predictors (BLUPs) were calculated across all field and growth chamber environments. A total of 73 marker-trait associations (MTAs) were detected on nine different chromosomes (1A, 2A, 2B, 4A, 5A, 5B, 7A, 7B and 7D) that were significantly associated (p-value <0.001) with eyespot resistance in Panel A, and 19 MTAs on nine different chromosomes (1A, 1B, 2A, 2D, 3B, 5A, 5B, 7A, and 7B) in Panel B. The most significant SNPs were associated with Pch1 and Pch2 resistance genes on the long arms of chromosome 7D and 7A. Most of the novel MTAs appeared to have a minor effect on reducing eyespot disease. Nevertheless, eyespot disease scores decreased as the number of resistance alleles increased. Seven SNP markers, significantly associated with reducing eyespot disease across environments and in the absence and presence of Pch1 were identified. These markers were located on chromosomes 2A (IWB8331), 5A (IWB73709), 5B (IWB47298), 7AS (IWB47160), 7B (IWB45005) and two SNPs (Ex_c44379_2509 and IAAV4340) had unknown map positions. The additive effect of the MTAs explained most of the remaining phenotypic variation not accounted for by Pch1 or Pch2. This study provides breeders with adapted germplasm and novel sources of eyespot resistance to be used in the development of superior cultivars with increased eyespot resistance.
机译:眼斑病是由土壤传播的坏死性真菌Yulundae和O. acuformis引起的,对小麦,大麦和黑麦具有重要的经济意义。西北太平洋(PNW)冬小麦(Triticum aestivum L.)生长在高降雨和冬季温和地区,最容易受到感染。这项研究的目的是确定与适应PNW的冬小麦抗视点性相关的新基因组区域。编写了两个469和399系的冬小麦研究小组,以进行美国冬小麦种质对眼斑抗性的第一批全基因组关联研究(GWAS)。这些面板使用Infinium 9K和90K iSelect SNP阵列进行基因分型。在为期两年的现场研究和重复的生长室试验中,对两个面板的抗病性进行了表型分析。使用生长室试验分别评估了尖吻鲈和雅兰藻的遗传抗性。在所有田间和生长室环境中都计算出了最佳线性无偏预测器(BLUP)。在9个不同的染色体(1A,2A,2B,4A,5A,5B,7A,7B和7D)上共检测到73个标记-性状关联(MTA),这些染色体与眼点抗性显着相关(p值<0.001) A板中的BNP和19个MTA分别位于B板中的9个不同染色体(1A,1B,2A,2D,3B,5A,5B,7A和7B)上。最重要的SNP长期与Pch1和Pch2抗性基因相关7D和7A染色体的臂。大多数新颖的MTA似乎对减轻眼点病的影响较小。然而,眼点疾病评分随着抗性等位基因数量的增加而降低。鉴定出了七个SNP标记物,这些标记物在整个环境中以及在Pch1不存在和不存在下与减少眼点疾病显着相关。这些标记位于2A(IWB8331),5A(IWB73709),5B(IWB47298),7AS(IWB47160),7B( IWB45005 )和2个SNP( Ex_c44379_2509 )和 IAAV4340 )的地图位置未知。 MTA的加性效应解释了 Pch1 Pch2 未解释的大多数剩余表型变异。这项研究为育种者提供了适应性强的种质和新的视斑抗性来源,可用于发展具有更高视斑抗性的优良品种。

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