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首页> 外文期刊>Theoretical and Applied Genetics >Genetic and comparative genomics mapping reveals that a powdery mildew resistance gene Ml3D232 originating from wild emmer co-segregates with an NBS-LRR analog in common wheat (Triticum aestivum L.)
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Genetic and comparative genomics mapping reveals that a powdery mildew resistance gene Ml3D232 originating from wild emmer co-segregates with an NBS-LRR analog in common wheat (Triticum aestivum L.)

机译:遗传和比较基因组学图谱揭示,源自野生emmer的白粉病抗性基因Ml3D232与NBS-LRR类似物在普通小麦(Triticum aestivum L.)中共分离。

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摘要

Powdery mildew caused by Blumeria graminis f. sp. tritici is one of the most important wheat diseases worldwide and breeding for resistance using diversified disease resistance genes is the most promising approach to prevent outbreaks of powdery mildew. A powdery mildew resistance gene, originating from wild emmer wheat (Triticum turgidum var. dicoccoides) accessions collected from Israel, has been transferred into the hexaploid wheat line 3D232 through crossing and backcrossing. Inoculation results with 21 B. graminis f. sp. tritici races indicated that 3D232 is resistant to all of the powdery mildew isolates tested. Genetic analyses of 3D232 using an F2 segregating population and F3 families indicated that a single dominant gene, Ml3D232, confers resistance in the host seedling stage. By applying molecular markers and bulked segregant analysis (BSA), we have identified polymorphic simple sequence repeats (SSR), expressed sequence tags (EST) and derived sequence tagged site (STS) markers to determine that the Ml3D232 is located on chromosome 5BL bin 0.59–0.76. Comparative genetic analyses using mapped EST markers and genome sequences of rice and Brachypodium established co-linearity of the Ml3D232 genomic region with a 1.4 Mb genomic region on Brachypodium distachyon chromosome 4, and a 1.2 Mb contig located on the Oryza sativa chromosome 9. Our comparative approach enabled us to develop new EST–STS markers and to delimit the genomic region carrying Ml3D232 to a 0.8 cM segment that is collinear with a 558 kb region on B. distachyon. Eight EST markers, including an NBS-LRR analog, co-segregated with Ml3D232 to provide a target site for fine genetic mapping, chromosome landing and map-based cloning of the powdery mildew resistance gene. This newly developed common wheat germplasm provides broad-spectrum resistance to powdery mildew and a valuable resource for wheat breeding programs.
机译:白粉病菌引起的白粉病f。 sp。小麦是世界上最重要的小麦疾病之一,利用多样化的抗病基因进行抗病育种是预防白粉病暴发的最有前途的方法。源自以色列的野生Emmer小麦(Triticum turgidum var。dicoccoides)品种的抗白粉病基因已通过杂交和回交转移到六倍体小麦品系3D232中。用21 B. graminis f。接种的结果。 sp。 Tritici种族表明3D232对所有测试的白粉病菌都有抵抗力。使用F2 隔离种群和F3 家族对3D232进行的遗传分析表明,单个显性基因Ml3D232在宿主苗期赋予抗性。通过应用分子标记和本体分离分析(BSA),我们确定了多态性简单序列重复(SSR),表达序列标签(EST)和派生序列标签位点(STS)标记,以确定Ml3D232是否位于5BL染色体bin 0.59上–0.76。使用映射的EST标记以及水稻和短枝po的基因组序列进行的比较遗传分析建立了Ml3D232基因组区域与短枝chy属4号染色体上的1.4 Mb基因组区域和Oryza sativa 9号染色体上的1.2 Mb重叠群的共线性。这种方法使我们能够开发新的EST-STS标记,并将携带Ml3D232的基因组区域划定为0.8 cM区段,该区段与狄氏梭菌上的558 kb区域共线。八个EST标记(包括NBS-LRR类似物)与Ml3D232共分离,从而为白粉病抗性基因的精细遗传作图,染色体着陆和基于图的克隆提供了目标位点。这种新近开发的普通小麦种质对白粉病具有广谱抗性,是小麦育种计划的宝贵资源。

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  • 来源
    《Theoretical and Applied Genetics》 |2010年第8期|1613-1621|共9页
  • 作者单位

    State Key Laboratory for Agrobiotechnology China Agricultural University Beijing 100193 People’s Republic of China;

    State Key Laboratory for Agrobiotechnology China Agricultural University Beijing 100193 People’s Republic of China;

    State Key Laboratory for Agrobiotechnology China Agricultural University Beijing 100193 People’s Republic of China;

    State Key Laboratory for Agrobiotechnology China Agricultural University Beijing 100193 People’s Republic of China;

    State Key Laboratory for Agrobiotechnology China Agricultural University Beijing 100193 People’s Republic of China;

    Key Laboratory for Biology of Plant Disease and Insect Pests Institute of Plant Protection Chinese Academy of Agricultural Science Beijing 100094 People’s Republic of China;

    Key Laboratory for Biology of Plant Disease and Insect Pests Institute of Plant Protection Chinese Academy of Agricultural Science Beijing 100094 People’s Republic of China;

    State Key Laboratory for Agrobiotechnology China Agricultural University Beijing 100193 People’s Republic of China;

    State Key Laboratory for Agrobiotechnology China Agricultural University Beijing 100193 People’s Republic of China;

    State Key Laboratory for Agrobiotechnology China Agricultural University Beijing 100193 People’s Republic of China;

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