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Molecular identification and chromosomal localization of new powdery mildew resistance gene Pm11 in oat

The appropriate selection of various traits in valuable plants is very important for modern plant breeding. Effective resistance to fungal diseases, such as powdery mildew, is an example of such a trait in oats. Marker-assisted selection is an important tool that reduces the time and cost of selecti...

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Autores principales: Ociepa, Tomasz, Okoń, Sylwia, Nucia, Aleksandra, Leśniowska-Nowak, Justyna, Paczos-Grzęda, Edyta, Bisaga, Maciej
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952345/
https://www.ncbi.nlm.nih.gov/pubmed/31570968
http://dx.doi.org/10.1007/s00122-019-03449-3
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author Ociepa, Tomasz
Okoń, Sylwia
Nucia, Aleksandra
Leśniowska-Nowak, Justyna
Paczos-Grzęda, Edyta
Bisaga, Maciej
author_facet Ociepa, Tomasz
Okoń, Sylwia
Nucia, Aleksandra
Leśniowska-Nowak, Justyna
Paczos-Grzęda, Edyta
Bisaga, Maciej
author_sort Ociepa, Tomasz
collection PubMed
description The appropriate selection of various traits in valuable plants is very important for modern plant breeding. Effective resistance to fungal diseases, such as powdery mildew, is an example of such a trait in oats. Marker-assisted selection is an important tool that reduces the time and cost of selection. The aims of the present study were the identification of dominant DArTseq markers associated with a new resistance gene, annotated as Pm11 and derived from Avena sterilis genotype CN113536, and the subsequent conversion of these markers into a PCR-based assay. Among the obtained 30,620 silicoDArT markers, 202 markers were highly associated with resistance in the analysed population. Of these, 71 were selected for potential conversion: 42 specific to resistant and 29 to susceptible individuals. Finally, 40 silicoDArT markers were suitable for primer design. From this pool, five markers, 3 for resistant and 2 for susceptible plants, were selected for product amplification in the expected groups. The developed method, based on 2 selection markers, provides certain identification of resistant and susceptible homozygotes. Also, the use of these markers allowed the determination of heterozygotes in the analysed population. Selected silicoDArT markers were also used for chromosomal localization of new resistance genes. Five out of 71 segregating silicoDArT markers for the Pm11 gene were found on the available consensus genetic map of oat. Five markers were placed on linkage groups corresponding to Mrg12 on the Avena sativa consensus map.
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spelling pubmed-69523452020-01-23 Molecular identification and chromosomal localization of new powdery mildew resistance gene Pm11 in oat Ociepa, Tomasz Okoń, Sylwia Nucia, Aleksandra Leśniowska-Nowak, Justyna Paczos-Grzęda, Edyta Bisaga, Maciej Theor Appl Genet Original Article The appropriate selection of various traits in valuable plants is very important for modern plant breeding. Effective resistance to fungal diseases, such as powdery mildew, is an example of such a trait in oats. Marker-assisted selection is an important tool that reduces the time and cost of selection. The aims of the present study were the identification of dominant DArTseq markers associated with a new resistance gene, annotated as Pm11 and derived from Avena sterilis genotype CN113536, and the subsequent conversion of these markers into a PCR-based assay. Among the obtained 30,620 silicoDArT markers, 202 markers were highly associated with resistance in the analysed population. Of these, 71 were selected for potential conversion: 42 specific to resistant and 29 to susceptible individuals. Finally, 40 silicoDArT markers were suitable for primer design. From this pool, five markers, 3 for resistant and 2 for susceptible plants, were selected for product amplification in the expected groups. The developed method, based on 2 selection markers, provides certain identification of resistant and susceptible homozygotes. Also, the use of these markers allowed the determination of heterozygotes in the analysed population. Selected silicoDArT markers were also used for chromosomal localization of new resistance genes. Five out of 71 segregating silicoDArT markers for the Pm11 gene were found on the available consensus genetic map of oat. Five markers were placed on linkage groups corresponding to Mrg12 on the Avena sativa consensus map. Springer Berlin Heidelberg 2019-09-30 2020 /pmc/articles/PMC6952345/ /pubmed/31570968 http://dx.doi.org/10.1007/s00122-019-03449-3 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Ociepa, Tomasz
Okoń, Sylwia
Nucia, Aleksandra
Leśniowska-Nowak, Justyna
Paczos-Grzęda, Edyta
Bisaga, Maciej
Molecular identification and chromosomal localization of new powdery mildew resistance gene Pm11 in oat
title Molecular identification and chromosomal localization of new powdery mildew resistance gene Pm11 in oat
title_full Molecular identification and chromosomal localization of new powdery mildew resistance gene Pm11 in oat
title_fullStr Molecular identification and chromosomal localization of new powdery mildew resistance gene Pm11 in oat
title_full_unstemmed Molecular identification and chromosomal localization of new powdery mildew resistance gene Pm11 in oat
title_short Molecular identification and chromosomal localization of new powdery mildew resistance gene Pm11 in oat
title_sort molecular identification and chromosomal localization of new powdery mildew resistance gene pm11 in oat
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6952345/
https://www.ncbi.nlm.nih.gov/pubmed/31570968
http://dx.doi.org/10.1007/s00122-019-03449-3
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