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Genes involved in barley yellow dwarf virus resistance of maize

KEY MESSAGE: The results of our study suggest that genes involved in general resistance mechanisms of plants contribute to variation of BYDV resistance in maize. ABSTRACT: With increasing winter temperatures in Europe, Barley yellow dwarf virus (BYDV) is expected to become a prominent problem in mai...

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Autores principales: Horn, Frederike, Habekuß, Antje, Stich, Benjamin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236618/
https://www.ncbi.nlm.nih.gov/pubmed/25261982
http://dx.doi.org/10.1007/s00122-014-2400-1
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author Horn, Frederike
Habekuß, Antje
Stich, Benjamin
author_facet Horn, Frederike
Habekuß, Antje
Stich, Benjamin
author_sort Horn, Frederike
collection PubMed
description KEY MESSAGE: The results of our study suggest that genes involved in general resistance mechanisms of plants contribute to variation of BYDV resistance in maize. ABSTRACT: With increasing winter temperatures in Europe, Barley yellow dwarf virus (BYDV) is expected to become a prominent problem in maize cultivation. Breeding for resistance is the best strategy to control the disease and break the transmission cycle of the virus. The objectives of our study were (1) to determine genetic variation with respect to BYDV resistance in a broad germplasm set and (2) to identify single nucleotide polymorphism (SNP) markers linked to genes that are involved in BYDV resistance. An association mapping population with 267 genotypes representing the world’s maize gene pool was grown in the greenhouse. Plants were inoculated with BYDV-PAV using viruliferous Rhopalosiphum padi. In the association mapping population, we observed considerable genotypic variance for the trait virus extinction as measured by double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) and the infection rate. In a genome-wide association study, we observed three SNPs significantly [false discovery rate (FDR) = 0.05] associated with the virus extinction on chromosome 10 explaining together 25 % of the phenotypic variance and five SNPs for the infection rate on chromosomes 4 and 10 explaining together 33 % of the phenotypic variance. The SNPs significantly associated with BYDV resistance can be used in marker assisted selection and will accelerate the breeding process for the development of BYDV resistant maize genotypes. Furthermore, these SNPs were located within genes which were in other organisms described to play a role in general resistance mechanisms. This suggests that these genes contribute to variation of BYDV resistance in maize. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-014-2400-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-42366182014-11-21 Genes involved in barley yellow dwarf virus resistance of maize Horn, Frederike Habekuß, Antje Stich, Benjamin Theor Appl Genet Original Paper KEY MESSAGE: The results of our study suggest that genes involved in general resistance mechanisms of plants contribute to variation of BYDV resistance in maize. ABSTRACT: With increasing winter temperatures in Europe, Barley yellow dwarf virus (BYDV) is expected to become a prominent problem in maize cultivation. Breeding for resistance is the best strategy to control the disease and break the transmission cycle of the virus. The objectives of our study were (1) to determine genetic variation with respect to BYDV resistance in a broad germplasm set and (2) to identify single nucleotide polymorphism (SNP) markers linked to genes that are involved in BYDV resistance. An association mapping population with 267 genotypes representing the world’s maize gene pool was grown in the greenhouse. Plants were inoculated with BYDV-PAV using viruliferous Rhopalosiphum padi. In the association mapping population, we observed considerable genotypic variance for the trait virus extinction as measured by double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) and the infection rate. In a genome-wide association study, we observed three SNPs significantly [false discovery rate (FDR) = 0.05] associated with the virus extinction on chromosome 10 explaining together 25 % of the phenotypic variance and five SNPs for the infection rate on chromosomes 4 and 10 explaining together 33 % of the phenotypic variance. The SNPs significantly associated with BYDV resistance can be used in marker assisted selection and will accelerate the breeding process for the development of BYDV resistant maize genotypes. Furthermore, these SNPs were located within genes which were in other organisms described to play a role in general resistance mechanisms. This suggests that these genes contribute to variation of BYDV resistance in maize. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-014-2400-1) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2014-09-28 2014 /pmc/articles/PMC4236618/ /pubmed/25261982 http://dx.doi.org/10.1007/s00122-014-2400-1 Text en © The Author(s) 2014 https://creativecommons.org/licenses/by/4.0/ Open AccessThis article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
spellingShingle Original Paper
Horn, Frederike
Habekuß, Antje
Stich, Benjamin
Genes involved in barley yellow dwarf virus resistance of maize
title Genes involved in barley yellow dwarf virus resistance of maize
title_full Genes involved in barley yellow dwarf virus resistance of maize
title_fullStr Genes involved in barley yellow dwarf virus resistance of maize
title_full_unstemmed Genes involved in barley yellow dwarf virus resistance of maize
title_short Genes involved in barley yellow dwarf virus resistance of maize
title_sort genes involved in barley yellow dwarf virus resistance of maize
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236618/
https://www.ncbi.nlm.nih.gov/pubmed/25261982
http://dx.doi.org/10.1007/s00122-014-2400-1
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