Association mapping of spot blotch resistance in wild barley

被引:124
作者
Roy, Joy K. [1 ]
Smith, Kevin P. [2 ]
Muehlbauer, Gary J. [2 ]
Chao, Shiaoman [3 ]
Close, Timothy J. [4 ]
Steffenson, Brian J. [1 ]
机构
[1] Univ Minnesota, Dept Plant Pathol, St Paul, MN 55108 USA
[2] Univ Minnesota, Dept Agron & Plant Genet, St Paul, MN 55108 USA
[3] USDA ARS, Biosci Res Lab, Fargo, ND 58105 USA
[4] Univ Calif Riverside, Dept Bot & Plant Sci, Riverside, CA 92521 USA
关键词
Hordeum vulgare subsp spontaneum; Quantitative trait loci (QTL); Population structure; Linkage disequilibrium mapping; SNP; DArT (R); MULTIPLE DISEASE RESISTANCE; MULTILOCUS GENOTYPE DATA; QUANTITATIVE TRAIT LOCI; LINKAGE DISEQUILIBRIUM; COCHLIOBOLUS-SATIVUS; POPULATION-STRUCTURE; HAPLOTYPE DIVERSITY; INFERENCE; POLYMORPHISMS; TECHNOLOGY;
D O I
10.1007/s11032-010-9402-8
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
Spot blotch, caused by Cochliobolus sativus, is an important foliar disease of barley. The disease has been controlled for over 40 years through the deployment of cultivars with durable resistance derived from the line NDB112. Pathotypes of C. sativus with virulence for the NDB112 resistance have been detected in Canada; thus, many commercial cultivars are vulnerable to spot blotch epidemics. To increase the diversity of spot blotch resistance in cultivated barley, we evaluated 318 diverse wild barley accessions comprising the Wild Barley Diversity Collection (WBDC) for reaction to C. sativus at the seedling stage and utilized an association mapping (AM) approach to identify and map resistance loci. A high frequency of resistance was found in the WBDC as 95% (302/318) of the accessions exhibited low infection responses. The WBDC was genotyped with 558 Diversity Array Technology (DArTA (R)) and 2,878 single nucleotide polymorphism (SNP) markers and subjected to structure analysis before running the AM procedure. Thirteen QTL for spot blotch resistance were identified with DArT and SNP markers. These QTL were found on chromosomes 1H, 2H, 3H, 5H, and 7H and explained from 2.3 to 3.9% of the phenotypic variance. Nearly half of the identified QTL mapped to chromosome bins where spot blotch resistance loci were previously reported, offering some validation for the AM approach. The other QTL mapped to unique genomic regions and may represent new spot blotch resistance loci. This study demonstrates that AM is an effective technique for identifying and mapping QTL for disease resistance in a wild crop progenitor.
引用
收藏
页码:243 / 256
页数:14
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