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Detection of Fusarium head blight resistance QTLs using five populations of top-cross progeny derived from two-row × two-row crosses in barley

机译:利用大麦两行×两行杂交获得的五个顶交后代群体检测镰刀菌抗白叶枯病QTL

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Fusarium head blight (FHB) resistance was evaluated in five recombinant inbred (RI) populations. The RI populations consisted of top-cross progeny derived from a diallel set of crosses. Each of five two-row barley lines differing in response to FHB were crossed with ‘Harbin 2-row’. FHB severity was scored on an 11-point scale, where resistant = 0 and susceptible = 10, based on the ‘cut-spike test’. Disease data were obtained for each population for 2 or 3 years. Linkage maps comprised of expressed sequence tag (EST) markers were developed for each population and used for quantitative trait locus (QTL) detection. Thirty two QTLs were detected using all data sets (individual populations and years). Thirteen QTLs were detected using averages across years; 10 of these were consistent across the individual year and average data sets. These QTLs clustered at 14 regions, with clusters on all chromosomes. At 11 of these clusters, Harbin 2-row contributed FHB resistance alleles. No QTLs were detected near the row type (vrs1) locus in any of the five RI populations, suggesting that the FHB resistance QTL in this region reported in two-row × six-row crosses may be pleiotropic effect of vrs1. QTL were coincident with the flowering type locus (cly1/Cly2) on chromosome 2H in every population. Some QTL × QTL interactions were significant, but these were smaller than QTL main effects. Considering the pleiotropic effect of spike morphology on FHB resistance, future FHB resistance mapping efforts in barley should focus on cross combinations in which alleles at vrs1 are not segregating.
机译:在五个重组近交(RI)群体中评估了镰刀菌的枯萎病(FHB)抗性。 RI群体由源自二叉杂交组的顶级杂交后代组成。在对FHB的反应不同的5行两行大麦中,每条都与“哈尔滨2行”交叉。 FHB严重程度是根据“割伤测试”以11分制进行评分的,其中抵抗力= 0,易感性= 10。获得每个人群2年或3年的疾病数据。为每个人群开发了由表达的序列标签(EST)标记组成的连锁图谱,并将其用于定量性状基因座(QTL)检测。使用所有数据集(个体人口和年份)检测到32个QTL。使用多年平均值检测了13个QTL;其中10个在各个年份和平均数据集上是一致的。这些QTL聚集在14个区域,并且在所有染色体上均聚集。在这些簇中的11个中,哈尔滨2行贡献了FHB抗性等位基因。在五个RI种群中,在行类型(vrs1)位点附近均未检测到QTL,这表明该区域以两行×六行杂交报道的FHB抗性QTL可能是vrs1的多效性效应。在每个人群中,QTL与2H染色体上的开花型基因座(cly1 / Cly2)一致。一些QTL×QTL相互作用是显着的,但小于QTL主要影响。考虑到穗形态对FHB抗性的多效性影响,未来大麦的FHB抗性作图工作应着眼于交叉组合,其中vrs1的等位基因不会分离。

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