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首页> 外文期刊>Theoretical and Applied Genetics >Identification and comparative mapping of a powdery mildew resistance gene derived from wild emmer (Triticum turgidum var. dicoccoides) on chromosome 2BS
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Identification and comparative mapping of a powdery mildew resistance gene derived from wild emmer (Triticum turgidum var. dicoccoides) on chromosome 2BS

机译:鉴定和比较图谱从野生Emmer(Triticum turgidum var.dicoccoides)产生的白粉病抗性基因在2BS染色体上

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摘要

Powdery mildew, caused by Blumeria graminis f. sp. tritici, is an important foliar disease of wheat worldwide. Wild emmer (Triticum turgidum var. dicoccoides) is a valuable genetic resource for improving disease resistance in common wheat. A powdery mildew resistance gene conferring resistance to B. graminis f. sp. tritici isolate E09 at the seedling and adult stages was identified in wild emmer accession IW170 introduced from Israel. An incomplete dominant gene, temporarily designated MlIW170, was responsible for the resistance. Through molecular marker and bulked segregant analyses of an F2 population and F3 families derived from a cross between susceptible durum wheat line 81086A and IW170, MlIW170 was located in the distal chromosome bin 2BS3-0.84-1.00 and flanked by SSR markers Xcfd238 and Xwmc243. MlIW170 co-segregated with Xcau516, an STS marker developed from RFLP marker Xwg516 that co-segregated with powdery mildew resistance gene Pm26 on 2BS. Four EST–STS markers, BE498358, BF201235, BQ160080, and BF146221, were integrated into the genetic linkage map of MlIW170. Three AFLP markers, XPaacMcac, XPagcMcta, XPaacMcag, and seven AFLP-derived SCAR markers, XcauG2, XcauG3, XcauG6, XcauG8, XcauG10, XcauG20, and XcauG25, were linked to MlIW170. XcauG3, a resistance gene analog (RGA)-like sequence, co-segregated with MlIW170. The non-glaucousness locus Iw1 was 18.77 cM distal to MlIW170. By comparative genomics of wheat–Brachypodium–rice genomic co-linearity, four EST–STS markers, CJ658408, CJ945509, BQ169830, CJ945085, and one STS marker XP2430, were developed and MlIW170 was mapped in an 2.69 cM interval that is co-linear with a 131 kb genomic region in Brachypodium and a 105 kb genomic region in rice. Four RGA-like sequences annotated in the orthologous Brachypodium genomic region could serve as chromosome landing target regions for map-based cloning of MlIW170.
机译:白粉病,由Blumeria graminis f。引起。 sp。小麦是世界范围内重要的小麦叶面疾病。野生Emmer(Triticum turgidum var。dicoccoides)是提高普通小麦抗病能力的宝贵遗传资源。赋予白粉病菌抗性的白粉病抗性基因。 sp。在从以色列引进的野生Emmer保藏号IW170中鉴定到了幼苗和成年期的小麦分离株E09。抵抗力是一个不完整的显性基因,暂时命名为MlIW170。通过对易感硬质小麦81086A与IW170杂交后代的F2 种群和F3 家族的分子标记和大量分离子分析,MlIW170位于远端染色体bin 2BS3-0.84-1.00并位于其两侧通过SSR标记Xcfd238和Xwmc243。 MlIW170与Xcau516共分离,Xcau516是从RFLP标记Xwg516开发的STS标记,与2BS上的白粉病抗性基因Pm26共分离。四个EST–STS标记BE498358,BF201235,BQ160080和BF146221已整合到MlIW170的遗传连锁图中。三个AFLP标记XPaacMcac,XPagcMcta,XPaacMcag和七个AFLP衍生的SCAR标记XcauG2,XcauG3,XcauG6,XcauG8,XcauG10,XcauG20和XcauG25被链接到MlIW170。 XcauG3,一种抗性基因类似物(RGA)样序列,与MlIW170共分离。非冰河性位点Iw1在M111W170的远端是18.77cM。通过比较小麦-Brachypodium-水稻基因组共线性的基因组学,开发了四个EST-STS标记CJ658408,CJ945509,BQ169830,CJ945085和一个STS标记XP2430,并在2.69 cM的共线性区间绘制了MlIW170在腕足动物中有131 kb的基因组区域,在水稻中有105 kb的基因组区域。在直系同源的短枝孢子基因组区域中注释的四个RGA样序列可以用作染色体着陆靶区域,用于基于图谱的M1IW170克隆。

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  • 来源
    《Theoretical and Applied Genetics》 |2012年第6期|1041-1049|共9页
  • 作者单位

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

    State Key Laboratory for Agrobiotechnology Beijing Key Laboratory of Crop Genetic Improvement Key Laboratory of Crop Heterosis Research and Utilization Department of Plant Genetics and Breeding China Agricultural University Beijing 100193 China;

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