Department of Plant Pathology, North Dakota State University, 58105, Fargo, ND, USA.
Theor Appl Genet. 1996 Apr;92(5):552-8. doi: 10.1007/BF00224557.
Net blotch (caused by Pyrenophora teres f. teres) and spot blotch (Cochliobolus sativus) are important foliar diseases of barley in the midwestern region of the USA. To determine the number and chromosomal location of Mendelian and quantitative trait loci (QTL) controlling resistance to these diseases, a doubled haploid population ('Steptoe'/'Morex') was evaluated to the pathogens at the seedling stage in the greenhouse and at the adult plant stage in the field. Alleles at two or three unlinked loci were found to confer resistance to the net blotch pathogen at the seedling stage depending on how progeny exhibiting an intermediate infection response were classified. This result was corroborated in the quantitative analysis of the raw infection response data as 2 major QTL were identified on chromosomes 4 and 6M. A third QTL was also identified on chromosome 6P. Seven QTL were identified for net blotch resistance at the adult plant stage and mapped to chromosomes 1P, 2P, 3P, 3M, 4, 6P, and 7P. The 7 QTL collectively accounted for 67.6% of the phenotypic variance under a multiple QTL model. Resistance to the spot blotch pathogen was conferred by a single gene at the seedling stage. This gene was mapped to the distal region of chromosome 1P on the basis of both qualitative and quantitative data analyses. Two QTL were identified for spot blotch resistance at the adult plant stage: the largest QTL effect mapped to chromosome 5P and the other mapped to chromosome 1P near the seedling resistance locus. Together, the 2 QTL explained 70.1% of the phenotypic variance under a multiple QTL model. On the basis of the chromosomal locations of resistance alleles detected in this study, it should be feasible to combine high levels of resistance to both P. teres f. teres and C. sativus in barley cultivars.
网斑病(由 Pyrenophora teres f. teres 引起)和斑点病(Cochliobolus sativus)是美国中西部地区大麦的重要叶部病害。为了确定控制这些疾病抗性的孟德尔和数量性状位点(QTL)的数量和染色体位置,利用一个双单倍体群体('Steptoe'/'Morex'),在温室幼苗期和田间成株期对病原体进行评估。根据中间感染反应的后代如何分类,发现两个或三个不连锁基因座的等位基因在幼苗期控制网斑病病原体的抗性。这一结果在对原始感染反应数据的定量分析中得到了证实,因为在第 4 和第 6M 染色体上鉴定出 2 个主要的 QTL。第 6P 染色体上也鉴定出第 3 个 QTL。在成株期鉴定出 7 个控制网斑病抗性的 QTL,并将其映射到第 1P、2P、3P、3M、4、6P 和 7P 染色体上。在多 QTL 模型下,这 7 个 QTL 共解释了 67.6%的表型方差。在幼苗期,斑点病病原体的抗性由单个基因赋予。该基因根据定性和定量数据分析,被映射到第 1P 染色体的远端区域。在成株期鉴定出 2 个控制斑点病抗性的 QTL:最大的 QTL 效应映射到第 5P 染色体,另一个映射到 1P 染色体,靠近幼苗抗性基因座。这 2 个 QTL 在多 QTL 模型下共解释了 70.1%的表型方差。根据本研究中检测到的抗性等位基因的染色体位置,在大麦品种中结合高水平的抗 Pyrenophora teres f. teres 和 Cochliobolus sativus 应该是可行的。