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Fine mapping, phenotypic characterization and validation of non-race-specific resistance to powdery mildew in a wheat–Triticum militinae introgression line

机译:小麦-小黑麦基因渗入系的精细定位,表型鉴定和对非种族特异性白粉病抗性的验证

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摘要

Introgression of several genomic loci from tetraploid Triticum militinae into bread wheat cv. T?hti has increased resistance of introgression line 8.1 to powdery mildew in seedlings and adult plants. In our previous work, only a major quantitative trait locus (QTL) on chromosome 4AL of the line 8.1 contributed significantly to resistance, whereas QTL on chromosomes 1A, 1B, 2A, 5A and 5B were detected merely on a suggestive level. To verify and characterize all QTLs in the line 8.1, a mapping population of double haploid lines was established. Testing for seedling resistance to 16 different races/mixtures of Blumeria graminis f. sp. tritici revealed four highly significant non-race-specific resistance QTL including the main QTL on chromosome 4AL, and a race-specific QTL on chromosome 5B. The major QTL on chromosome 4AL (QPm.tut-4A) as well as QTL on chromosome 5AL and a newly detected QTL on 7AL were highly effective at the adult stage. The QPm.tut-4A QTL accounts on average for 33–49 % of the variation in resistance in the double haploid population. Interactions between the main QTL QPm.tut-4A and the minor QTL were evaluated and discussed. A population of 98 F2 plants from a cross of susceptible cv. Chinese Spring and the line 8.1 was created that allowed mapping the QPm.tut-4A locus to the proximal 2.5-cM region of the introgressed segment on chromosome 4AL. The results obtained in this work make it feasible to use QPm.tut-4A in resistance breeding and provide a solid basis for positional cloning of the major QTL.
机译:从四倍体小麦中的几个基因组基因座渗入面包小麦简历中。 T?hti增加了渗入系8.1对幼苗和成年植物中白粉病的抗性。在我们之前的工作中,仅8.1系4AL染色体上的主要数量性状基因座(QTL)对耐药产生了显着贡献,而仅在提示水平上检测到1A,1B,2A,5A和5B染色体上的QTL。为了验证和鉴定品系8.1中的所有QTL,建立了双单倍体品系的作图群体。测试幼苗对Blumeria graminis f的16种不同种族/混合物的抗性。 sp。 Tritici揭示了四个高度重要的非种族特异性抗性QTL,包括4AL染色体上的主要QTL和5B染色体上的种族特异性QTL。在成年阶段,4AL染色体上的主要QTL(QPm.tut-4A)以及5AL染色体上的QTL和7AL上新检测到的QTL都非常有效。 QPm.tut-4A QTL平均占双单倍体种群抗性变化的33–49%。主要QTL QPm.tut-4A与次要QTL之间的相互作用已得到评估和讨论。来自易感简历的98个F2 植物种群。创建了Chinese Spring和line 8.1,它允许将QPm.tut-4A基因座映射到4AL染色体上渐渗区段的近端2.5-cM区。这项工作获得的结果使在抗性育种中使用QPm.tut-4A成为可能,并为主要QTL的位置克隆提供了坚实的基础。

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  • 来源
    《Theoretical and Applied Genetics》 |2012年第3期|609-623|共15页
  • 作者单位

    Department of Gene Technology Tallinn University of Technology Akadeemia tee 15 12618 Tallinn Estonia;

    Department of Gene Technology Tallinn University of Technology Akadeemia tee 15 12618 Tallinn Estonia;

    Department of Gene Technology Tallinn University of Technology Akadeemia tee 15 12618 Tallinn Estonia;

    Department of Gene Technology Tallinn University of Technology Akadeemia tee 15 12618 Tallinn Estonia;

    Department of Gene Technology Tallinn University of Technology Akadeemia tee 15 12618 Tallinn Estonia;

    Centre of the Region Haná for Biotechnological and Agricultural Research Institute of Experimental Botany Sokolovska 6 77200 Olomouc Czech Republic;

    Centre of the Region Haná for Biotechnological and Agricultural Research Institute of Experimental Botany Sokolovska 6 77200 Olomouc Czech Republic;

    Centre of the Region Haná for Biotechnological and Agricultural Research Institute of Experimental Botany Sokolovska 6 77200 Olomouc Czech Republic;

    Centre of the Region Haná for Biotechnological and Agricultural Research Institute of Experimental Botany Sokolovska 6 77200 Olomouc Czech Republic;

    Department of Gene Technology Tallinn University of Technology Akadeemia tee 15 12618 Tallinn Estonia;

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