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首页> 外文期刊>Theoretical and Applied Genetics >Development of functional markers specific for seven Pm3 resistance alleles and their validation in the bread wheat gene pool
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Development of functional markers specific for seven Pm3 resistance alleles and their validation in the bread wheat gene pool

机译:七个Pm3抗性等位基因特异功能标记的开发及其在面包小麦基因库中的验证

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摘要

In the ideal case, molecular markers used for marker-assisted selection are allele-specific even if the alleles differ only by a few nucleotide polymorphisms within the coding sequence of target genes. Such ‘perfect’ markers are completely correlated with the trait of interest. In hexaploid wheat (Triticum aestivum L.) the Pm3 locus encodes seven alleles (Pm3a–Pm3g) conferring resistance to different races of Blumeria graminis f.sp. tritici, the agent of powdery mildew, a major disease of bread wheat. All Pm3 alleles are known at the molecular level. Here, we generated specific markers for the Pm3 alleles based on nucleotide polymorphisms of coding and adjacent non-coding regions. The specificity of these markers was validated in a collection of 93 modern or historically important cultivars and breeding lines of wheat and spelt (Triticum spelta L.). These markers confirmed the presence of the predicted Pm3 alleles in 31 varieties and lines known to carry Pm3 resistance alleles. In a few varieties, Pm3 alleles different from alleles previously described based on pathogenicity tests or tightly linked markers were observed. In all these cases, the identity of the marker-detected Pm3 alleles was confirmed by DNA sequence analysis. Pm3 markers confirmed the absence of known Pm3 resistance alleles in 54 European wheat and spelt varieties in which Pm3 alleles had not been previously identified. These results indicate that the developed markers are highly diagnostic for specific Pm3 resistance alleles in a wide range of varieties and breeding lines, and will be useful (1) for identifying Pm3 alleles in the wheat gene pool, (2) for efficient marker-assisted selection of these genes, and (3) for combining multiple Pm3 alleles within a single cultivar through transgenic approaches.
机译:在理想情况下,用于标记辅助选择的分子标记是等位基因特异性的,即使等位基因仅在靶基因编码序列内的几个核苷酸多态性之间存在差异。这样的“完美”标记与兴趣特征完全相关。在六倍体小麦(Triticum aestivum L.)中,Pm3基因座编码七个等位基因(Pm3a–Pm3g),赋予了对不同等级的Blumeria graminis f.sp.的抗性。小麦,白粉病的主要病因是小麦。所有Pm3等位基因在分子水平上都是已知的。在这里,我们基于编码和相邻非编码区的核苷酸多态性,为Pm3等位基因生成了特异性标记。这些标记的特异性已在93个现代或历史上重要的小麦和拼写(Triticum spelta L.)品种和育种系中得到验证。这些标记物证实了在已知携带Pm3抗性等位基因的31个变种和品系中存在预测的Pm3等位基因。在一些变种中,观察到与先前基于致病性测试或紧密连锁的标记描述的等位基因不同的Pm3等位基因。在所有这些情况下,通过DNA序列分析证实了标记物检测到的Pm3等位基因的身份。 Pm3标记证实了54个欧洲小麦和先前未鉴定出Pm3等位基因的拼写品种中不存在已知的Pm3抗性等位基因。这些结果表明,已开发的标记物可对多种变种和育种系中的特定Pm3抗性等位基因进行高度诊断,并将对(1)鉴定小麦基因库中的Pm3等位基因,(2)用于有效的标记辅助方法具有很高的诊断价值。这些基因的选择,以及(3)通过转基因方法在单个品种中组合多个Pm3等位基因。

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  • 来源
    《Theoretical and Applied Genetics》 |2006年第1期|165-175|共11页
  • 作者单位

    Plant Molecular Biology Department Institute of Plant Biology University of ZürichDepartment of Botany and Plant Sciences University of California;

    Plant Molecular Biology Department Institute of Plant Biology University of Zürich;

    Plant Molecular Biology Department Institute of Plant Biology University of ZürichUbon Ratchathani Rice Research Center;

    Plant Molecular Biology Department Institute of Plant Biology University of Zürich;

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