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首页> 外文期刊>BMC Plant Biology >Highly predictive SNP markers for efficient selection of the wheat leaf rust resistance gene Lr16
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Highly predictive SNP markers for efficient selection of the wheat leaf rust resistance gene Lr16

机译:高效预测小麦叶片抗锈性基因Lr16的高预测性SNP标记

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摘要

Background Lr16 is a widely deployed leaf rust resistance gene in wheat ( Triticum aestivum L.) that is highly effective against the North American Puccinia triticina population when pyramided with the gene Lr34. Lr16 is a seedling leaf rust resistance gene conditioning an incompatible interaction with a distinct necrotic ring surrounding the uredinium. Lr16 was previously mapped to the telomeric region of the short arm of wheat chromosome 2B. The goals of this study were to develop numerous single nucleotide polymorphism (SNP) markers for the Lr16 region and identify diagnostic gene-specific SNP marker assays for marker-assisted selection (MAS). Results Forty-three SNP markers were developed and mapped on chromosome 2BS tightly linked with the resistance gene Lr16 across four mapping populations representing a total of 1528 gametes. Kompetitive Allele Specific PCR (KASP) assays were designed for all identified SNPs. Resistance gene analogs (RGAs) linked with the Lr16 locus were identified and RGA-based SNP markers were developed. The diagnostic potential of the SNPs co-segregating with Lr16 was evaluated in a diverse set of 133 cultivars and breeding lines. Six SNP markers were consistent with the Lr16 phenotype and are accurately predictive of Lr16 for all wheat lines/cultivars in the panel. Conclusions Lr16 was mapped relative to SNP markers in four populations. Six SNP markers exhibited high quality clustering in the KASP assay and are suitable for MAS of Lr16 in wheat breeding programs.
机译:背景技术Lr16是小麦(Triticum aestivum L.)中广泛使用的抗叶锈基因,当与基因Lr34形成金字塔状时,它对北美小麦锈菌群体非常有效。 Lr16是一种幼苗叶片抗锈基因,其条件是与围绕尿素的独特坏死环发生不相容的相互作用。 Lr16以前被映射到小麦2B号染色体短臂的端粒区域。这项研究的目标是为Lr16区开发许多单核苷酸多态性(SNP)标记,并鉴定用于标记辅助选择(MAS)的诊断基因特异性SNP标记测定。结果开发了43个SNP标记,并在与抗性基因Lr16紧密相关的2BS染色体上作图,分布在四个作图群体中,共计1528个配子。竞争性等位基因特异性PCR(KASP)分析法设计用于所有已鉴定的SNP。鉴定了与Lr16基因座相关的抗性基因类似物(RGA),并开发了基于RGA的SNP标记。在133个品种和育种系中评估了与Lr16共分离的SNP的诊断潜力。六个SNP标记与Lr16表型一致,并且可以准确预测小组中所有小麦品系/品种的Lr16。结论Lr16相对于SNP标记在四个人群中作图。六个SNP标记在KASP分析中表现出高质量的聚类,并且适合小麦育种计划中Lr16的MAS。

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