Agriculture and Agri-Food Canada, Cereal Research Centre, 101 Route 100, Morden, MB, R6M 1Y5, Canada.
Theor Appl Genet. 2015 Feb;128(2):247-58. doi: 10.1007/s00122-014-2425-5. Epub 2014 Nov 30.
Genetic analysis and genome mapping of a major seedling oat crown rust resistance gene, designated PcKM, are described. The chromosomal location of the PcKM gene was identified and linked markers were validated. Crown rust (Puccinia coronata Corda f. sp. avenae Eriks) is the most important foliar disease of oats and can cause considerable yield loss in the absence of appropriate management practices. Utilization of novel resistant genes is the most effective, economic and environmentally sound approach to control the disease. Crown rust resistance present in the cultivar 'Morton' was evaluated in a population developed from the cross OT3019 × 'Morton' to elucidate the genetic basis of resistance. Crown rust reaction evaluated in field nurseries and greenhouse tests demonstrated that resistance provided by 'Morton' was controlled by a single gene, temporarily designated as PcKM. The gene was initially linked to a random amplified polymorphic DNA band and subsequently converted into a sequence characterized amplified region (SCAR) marker. Genotyping with the PcKM SCAR on the 'Kanota' × 'Ogle' population, used to create the first oat chromosome-anchored linkage map, placed the PcKM gene on chromosome 12D. Consensus map markers present in the same region as the PcKM SCAR were tested on the OT3019 × 'Morton' population and two additional phenotyped populations segregating for PcKM to identify other markers useful for marker-assisted selection. Three markers were perfectly linked to the PcKM phenotype from which TaqMan and KBioscience competitive allele-specific PCR assays were developed and validated on a set of 25 oat lines. The assays correctly identified PcKM carriers. The markers developed in this study will facilitate fine mapping of the PcKM gene and simplify selection for this crown rust resistance.
主要的燕麦冠锈病抗性基因 PcKM 的遗传分析和基因组作图描述如下。PcKM 基因的染色体定位已被确定,并验证了连锁标记。冠锈病(Puccinia coronata Corda f. sp. avenae Eriks)是燕麦最重要的叶部病害,如果没有适当的管理措施,会导致相当大的产量损失。利用新的抗性基因是控制该病害最有效、经济和环保的方法。对品种 'Morton' 中存在的冠锈病抗性进行了评价,该品种是由 OT3019×'Morton'杂交产生的群体中进行的,以阐明抗性的遗传基础。在田间苗圃和温室试验中对冠锈病反应的评价表明,'Morton'提供的抗性由单个基因控制,该基因暂时命名为 PcKM。该基因最初与随机扩增多态性 DNA 带连锁,随后转化为序列特征扩增区 (SCAR) 标记。利用 'Kanota'×'Ogle'群体(用于创建第一个燕麦染色体锚定连锁图谱)对 PcKM SCAR 进行基因分型,将 PcKM 基因定位在 12D 染色体上。在 'OT3019×'Morton'群体中,对与 PcKM SCAR 位于同一区域的共识图谱标记进行了测试,并对另外两个分离出 PcKM 的表型群体进行了测试,以鉴定其他对标记辅助选择有用的标记。从 PcKM 表型中筛选出三个与 TaqMan 和 KBioscience 竞争等位基因特异性 PCR 检测试剂盒完全连锁的标记,并在一组 25 个燕麦品系上进行了验证。这些检测试剂盒正确地鉴定了 PcKM 携带者。本研究中开发的标记将有助于 PcKM 基因的精细作图,并简化对该冠锈病抗性的选择。