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High-resolution mapping of Rym14(Hb), a wild relative resistance gene to barley yellow mosaic disease

KEY MESSAGE: We mapped the Rym14(Hb) resistance locus to barley yellow mosaic disease in a 2Mbp interval. The co-segregating markers will be instrumental for marker-assisted selection in barley breeding. ABSTRACT: Barley yellow mosaic disease is caused by Barley yellow mosaic virus and Barley mild m...

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Detalles Bibliográficos
Autores principales: Pidon, Hélène, Wendler, Neele, Habekuβ, Antje, Maasberg, Anja, Ruge-Wehling, Brigitte, Perovic, Dragan, Ordon, Frank, Stein, Nils
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7925471/
https://www.ncbi.nlm.nih.gov/pubmed/33263784
http://dx.doi.org/10.1007/s00122-020-03733-7
Descripción
Sumario:KEY MESSAGE: We mapped the Rym14(Hb) resistance locus to barley yellow mosaic disease in a 2Mbp interval. The co-segregating markers will be instrumental for marker-assisted selection in barley breeding. ABSTRACT: Barley yellow mosaic disease is caused by Barley yellow mosaic virus and Barley mild mosaic virus and leads to severe yield losses in barley (Hordeum vulgare) in Central Europe and East-Asia. Several resistance loci are used in barley breeding. However, cases of resistance-breaking viral strains are known, raising concerns about the durability of those genes. Rym14(Hb) is a dominant major resistance gene on chromosome 6HS, originating from barley’s secondary genepool wild relative Hordeum bulbosum. As such, the resistance mechanism may represent a case of non-host resistance, which could enhance its durability. A susceptible barley variety and a resistant H. bulbosum introgression line were crossed to produce a large F(2) mapping population (n = 7500), to compensate for a ten-fold reduction in recombination rate compared to intraspecific barley crosses. After high-throughput genotyping, the Rym14(Hb) locus was assigned to a 2Mbp telomeric interval on chromosome 6HS. The co-segregating markers developed in this study can be used for marker-assisted introgression of this locus into barley elite germplasm with a minimum of linkage drag. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00122-020-03733-7) contains supplementary material, which is available to authorized users.