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Assessment of genetic diversity in Nordic timothy (Phleum pratense L.)
BACKGROUND: Timothy (Phleum pratense L.), a cool-season hexaploid perennial, is the most important forage grass species in Nordic countries. Earlier analyses of genetic diversity in a collection of 96 genebank accessions of timothy with SSR markers demonstrated high levels of diversity but could not...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226114/ https://www.ncbi.nlm.nih.gov/pubmed/28096767 http://dx.doi.org/10.1186/s41065-016-0009-x |
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author | Tanhuanpää, Pirjo Erkkilä, Maria Kalendar, Ruslan Schulman, Alan Howard Manninen, Outi |
author_facet | Tanhuanpää, Pirjo Erkkilä, Maria Kalendar, Ruslan Schulman, Alan Howard Manninen, Outi |
author_sort | Tanhuanpää, Pirjo |
collection | PubMed |
description | BACKGROUND: Timothy (Phleum pratense L.), a cool-season hexaploid perennial, is the most important forage grass species in Nordic countries. Earlier analyses of genetic diversity in a collection of 96 genebank accessions of timothy with SSR markers demonstrated high levels of diversity but could not resolve population structure. Therefore, we examined a subset of 51 accessions with REMAP markers, which are based on retrotransposons, and compared the diversity results with those obtained with SSR markers. RESULTS: Using four primer combinations, 533 REMAP markers were analyzed, compared with 464 polymorphic alleles in the 13 SSR loci previously. The average marker index, which describes information obtained per experiment (per primer combination or locus) was over six times higher with REMAPs. Most of the variation found was within accessions, with somewhat less, 89 %, for REMAPs, than for SSR, with 93 %. CONCLUSIONS: SSRs revealed differences in the level of diversity slightly better than REMAPs but neither marker type could reveal any clear clustering of accessions based on countries, vegetation zones, or different cultivar types. In our study, reliable evaluation of SSR allele dosages was not possible, so each allele had to be handled as a dominant marker. SSR and REMAP, which report from different mechanisms of generating genetic diversity and from different genomic regions, together indicate a lack of population structure. Taken together, this likely reflects the outcrossing and hexaploid nature of timothy rather than failures of either marker system. |
format | Online Article Text |
id | pubmed-5226114 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-52261142017-01-17 Assessment of genetic diversity in Nordic timothy (Phleum pratense L.) Tanhuanpää, Pirjo Erkkilä, Maria Kalendar, Ruslan Schulman, Alan Howard Manninen, Outi Hereditas Research BACKGROUND: Timothy (Phleum pratense L.), a cool-season hexaploid perennial, is the most important forage grass species in Nordic countries. Earlier analyses of genetic diversity in a collection of 96 genebank accessions of timothy with SSR markers demonstrated high levels of diversity but could not resolve population structure. Therefore, we examined a subset of 51 accessions with REMAP markers, which are based on retrotransposons, and compared the diversity results with those obtained with SSR markers. RESULTS: Using four primer combinations, 533 REMAP markers were analyzed, compared with 464 polymorphic alleles in the 13 SSR loci previously. The average marker index, which describes information obtained per experiment (per primer combination or locus) was over six times higher with REMAPs. Most of the variation found was within accessions, with somewhat less, 89 %, for REMAPs, than for SSR, with 93 %. CONCLUSIONS: SSRs revealed differences in the level of diversity slightly better than REMAPs but neither marker type could reveal any clear clustering of accessions based on countries, vegetation zones, or different cultivar types. In our study, reliable evaluation of SSR allele dosages was not possible, so each allele had to be handled as a dominant marker. SSR and REMAP, which report from different mechanisms of generating genetic diversity and from different genomic regions, together indicate a lack of population structure. Taken together, this likely reflects the outcrossing and hexaploid nature of timothy rather than failures of either marker system. BioMed Central 2016-04-26 /pmc/articles/PMC5226114/ /pubmed/28096767 http://dx.doi.org/10.1186/s41065-016-0009-x Text en © Tanhuanpää et al. 2016 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Tanhuanpää, Pirjo Erkkilä, Maria Kalendar, Ruslan Schulman, Alan Howard Manninen, Outi Assessment of genetic diversity in Nordic timothy (Phleum pratense L.) |
title | Assessment of genetic diversity in Nordic timothy (Phleum pratense L.) |
title_full | Assessment of genetic diversity in Nordic timothy (Phleum pratense L.) |
title_fullStr | Assessment of genetic diversity in Nordic timothy (Phleum pratense L.) |
title_full_unstemmed | Assessment of genetic diversity in Nordic timothy (Phleum pratense L.) |
title_short | Assessment of genetic diversity in Nordic timothy (Phleum pratense L.) |
title_sort | assessment of genetic diversity in nordic timothy (phleum pratense l.) |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5226114/ https://www.ncbi.nlm.nih.gov/pubmed/28096767 http://dx.doi.org/10.1186/s41065-016-0009-x |
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