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Association mapping of spot blotch resistance in wild barley

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 be...

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Autores principales: Roy, Joy K., Smith, Kevin P., Muehlbauer, Gary J., Chao, Shiaoman, Close, Timothy J., Steffenson, Brian J.
Formato: Texto
Lenguaje:English
Publicado: Springer Netherlands 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908432/
https://www.ncbi.nlm.nih.gov/pubmed/20694035
http://dx.doi.org/10.1007/s11032-010-9402-8
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author Roy, Joy K.
Smith, Kevin P.
Muehlbauer, Gary J.
Chao, Shiaoman
Close, Timothy J.
Steffenson, Brian J.
author_facet Roy, Joy K.
Smith, Kevin P.
Muehlbauer, Gary J.
Chao, Shiaoman
Close, Timothy J.
Steffenson, Brian J.
author_sort Roy, Joy K.
collection PubMed
description 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 (DArT(®)) 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11032-010-9402-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-29084322010-08-06 Association mapping of spot blotch resistance in wild barley Roy, Joy K. Smith, Kevin P. Muehlbauer, Gary J. Chao, Shiaoman Close, Timothy J. Steffenson, Brian J. Mol Breed Article 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 (DArT(®)) 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. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11032-010-9402-8) contains supplementary material, which is available to authorized users. Springer Netherlands 2010-03-10 2010 /pmc/articles/PMC2908432/ /pubmed/20694035 http://dx.doi.org/10.1007/s11032-010-9402-8 Text en © The Author(s) 2010 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Article
Roy, Joy K.
Smith, Kevin P.
Muehlbauer, Gary J.
Chao, Shiaoman
Close, Timothy J.
Steffenson, Brian J.
Association mapping of spot blotch resistance in wild barley
title Association mapping of spot blotch resistance in wild barley
title_full Association mapping of spot blotch resistance in wild barley
title_fullStr Association mapping of spot blotch resistance in wild barley
title_full_unstemmed Association mapping of spot blotch resistance in wild barley
title_short Association mapping of spot blotch resistance in wild barley
title_sort association mapping of spot blotch resistance in wild barley
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908432/
https://www.ncbi.nlm.nih.gov/pubmed/20694035
http://dx.doi.org/10.1007/s11032-010-9402-8
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