Cargando…
High-density marker profiling confirms ancestral genomes of Avena species and identifies D-genome chromosomes of hexaploid oat
KEY MESSAGE: Genome analysis of 27 oat species identifies ancestral groups, delineates the D genome, and identifies ancestral origin of 21 mapped chromosomes in hexaploid oat. ABSTRACT: We investigated genomic relationships among 27 species of the genus Avena using high-density genetic markers revea...
Autores principales: | , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069325/ https://www.ncbi.nlm.nih.gov/pubmed/27522358 http://dx.doi.org/10.1007/s00122-016-2762-7 |
_version_ | 1782460912045654016 |
---|---|
author | Yan, Honghai Bekele, Wubishet A. Wight, Charlene P. Peng, Yuanying Langdon, Tim Latta, Robert G. Fu, Yong-Bi Diederichsen, Axel Howarth, Catherine J. Jellen, Eric N. Boyle, Brian Wei, Yuming Tinker, Nicholas A. |
author_facet | Yan, Honghai Bekele, Wubishet A. Wight, Charlene P. Peng, Yuanying Langdon, Tim Latta, Robert G. Fu, Yong-Bi Diederichsen, Axel Howarth, Catherine J. Jellen, Eric N. Boyle, Brian Wei, Yuming Tinker, Nicholas A. |
author_sort | Yan, Honghai |
collection | PubMed |
description | KEY MESSAGE: Genome analysis of 27 oat species identifies ancestral groups, delineates the D genome, and identifies ancestral origin of 21 mapped chromosomes in hexaploid oat. ABSTRACT: We investigated genomic relationships among 27 species of the genus Avena using high-density genetic markers revealed by genotyping-by-sequencing (GBS). Two methods of GBS analysis were used: one based on tag-level haplotypes that were previously mapped in cultivated hexaploid oat (A. sativa), and one intended to sample and enumerate tag-level haplotypes originating from all species under investigation. Qualitatively, both methods gave similar predictions regarding the clustering of species and shared ancestral genomes. Furthermore, results were consistent with previous phylogenies of the genus obtained with conventional approaches, supporting the robustness of whole genome GBS analysis. Evidence is presented to justify the final and definitive classification of the tetraploids A. insularis, A. maroccana (=A. magna), and A. murphyi as containing D-plus-C genomes, and not A-plus-C genomes, as is most often specified in past literature. Through electronic painting of the 21 chromosome representations in the hexaploid oat consensus map, we show how the relative frequency of matches between mapped hexaploid-derived haplotypes and AC (DC)-genome tetraploids vs. A- and C-genome diploids can accurately reveal the genome origin of all hexaploid chromosomes, including the approximate positions of inter-genome translocations. Evidence is provided that supports the continued classification of a diverged B genome in AB tetraploids, and it is confirmed that no extant A-genome diploids, including A. canariensis, are similar enough to the D genome of tetraploid and hexaploid oat to warrant consideration as a D-genome diploid. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-016-2762-7) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5069325 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-50693252016-11-02 High-density marker profiling confirms ancestral genomes of Avena species and identifies D-genome chromosomes of hexaploid oat Yan, Honghai Bekele, Wubishet A. Wight, Charlene P. Peng, Yuanying Langdon, Tim Latta, Robert G. Fu, Yong-Bi Diederichsen, Axel Howarth, Catherine J. Jellen, Eric N. Boyle, Brian Wei, Yuming Tinker, Nicholas A. Theor Appl Genet Original Article KEY MESSAGE: Genome analysis of 27 oat species identifies ancestral groups, delineates the D genome, and identifies ancestral origin of 21 mapped chromosomes in hexaploid oat. ABSTRACT: We investigated genomic relationships among 27 species of the genus Avena using high-density genetic markers revealed by genotyping-by-sequencing (GBS). Two methods of GBS analysis were used: one based on tag-level haplotypes that were previously mapped in cultivated hexaploid oat (A. sativa), and one intended to sample and enumerate tag-level haplotypes originating from all species under investigation. Qualitatively, both methods gave similar predictions regarding the clustering of species and shared ancestral genomes. Furthermore, results were consistent with previous phylogenies of the genus obtained with conventional approaches, supporting the robustness of whole genome GBS analysis. Evidence is presented to justify the final and definitive classification of the tetraploids A. insularis, A. maroccana (=A. magna), and A. murphyi as containing D-plus-C genomes, and not A-plus-C genomes, as is most often specified in past literature. Through electronic painting of the 21 chromosome representations in the hexaploid oat consensus map, we show how the relative frequency of matches between mapped hexaploid-derived haplotypes and AC (DC)-genome tetraploids vs. A- and C-genome diploids can accurately reveal the genome origin of all hexaploid chromosomes, including the approximate positions of inter-genome translocations. Evidence is provided that supports the continued classification of a diverged B genome in AB tetraploids, and it is confirmed that no extant A-genome diploids, including A. canariensis, are similar enough to the D genome of tetraploid and hexaploid oat to warrant consideration as a D-genome diploid. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00122-016-2762-7) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-08-13 2016 /pmc/articles/PMC5069325/ /pubmed/27522358 http://dx.doi.org/10.1007/s00122-016-2762-7 Text en © The Author(s) 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. |
spellingShingle | Original Article Yan, Honghai Bekele, Wubishet A. Wight, Charlene P. Peng, Yuanying Langdon, Tim Latta, Robert G. Fu, Yong-Bi Diederichsen, Axel Howarth, Catherine J. Jellen, Eric N. Boyle, Brian Wei, Yuming Tinker, Nicholas A. High-density marker profiling confirms ancestral genomes of Avena species and identifies D-genome chromosomes of hexaploid oat |
title | High-density marker profiling confirms ancestral genomes of Avena species and identifies D-genome chromosomes of hexaploid oat |
title_full | High-density marker profiling confirms ancestral genomes of Avena species and identifies D-genome chromosomes of hexaploid oat |
title_fullStr | High-density marker profiling confirms ancestral genomes of Avena species and identifies D-genome chromosomes of hexaploid oat |
title_full_unstemmed | High-density marker profiling confirms ancestral genomes of Avena species and identifies D-genome chromosomes of hexaploid oat |
title_short | High-density marker profiling confirms ancestral genomes of Avena species and identifies D-genome chromosomes of hexaploid oat |
title_sort | high-density marker profiling confirms ancestral genomes of avena species and identifies d-genome chromosomes of hexaploid oat |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5069325/ https://www.ncbi.nlm.nih.gov/pubmed/27522358 http://dx.doi.org/10.1007/s00122-016-2762-7 |
work_keys_str_mv | AT yanhonghai highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT bekelewubisheta highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT wightcharlenep highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT pengyuanying highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT langdontim highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT lattarobertg highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT fuyongbi highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT diederichsenaxel highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT howarthcatherinej highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT jellenericn highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT boylebrian highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT weiyuming highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat AT tinkernicholasa highdensitymarkerprofilingconfirmsancestralgenomesofavenaspeciesandidentifiesdgenomechromosomesofhexaploidoat |