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Post-polyploidisation morphotype diversification associates with gene copy number variation
Genetic models for polyploid crop adaptation provide important information relevant for future breeding prospects. A well-suited model is Brassica napus, a recent allopolyploid closely related to Arabidopsis thaliana. Flowering time is a major adaptation trait determining life cycle synchronization...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292959/ https://www.ncbi.nlm.nih.gov/pubmed/28165502 http://dx.doi.org/10.1038/srep41845 |
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author | Schiessl, Sarah Huettel, Bruno Kuehn, Diana Reinhardt, Richard Snowdon, Rod |
author_facet | Schiessl, Sarah Huettel, Bruno Kuehn, Diana Reinhardt, Richard Snowdon, Rod |
author_sort | Schiessl, Sarah |
collection | PubMed |
description | Genetic models for polyploid crop adaptation provide important information relevant for future breeding prospects. A well-suited model is Brassica napus, a recent allopolyploid closely related to Arabidopsis thaliana. Flowering time is a major adaptation trait determining life cycle synchronization with the environment. Here we unravel natural genetic variation in B. napus flowering time regulators and investigate associations with evolutionary diversification into different life cycle morphotypes. Deep sequencing of 35 flowering regulators was performed in 280 diverse B. napus genotypes. High sequencing depth enabled high-quality calling of single-nucleotide polymorphisms (SNPs), insertion-deletions (InDels) and copy number variants (CNVs). By combining these data with genotyping data from the Brassica 60 K Illumina® Infinium SNP array, we performed a genome-wide marker distribution analysis across the 4 ecogeographical morphotypes. Twelve haplotypes, including Bna.FLC.A10, Bna.VIN3.A02 and the Bna.FT promoter on C02_random, were diagnostic for the diversification of winter and spring types. The subspecies split between oilseed/kale (B. napus ssp. napus) and swedes/rutabagas (B. napus ssp. napobrassica) was defined by 13 haplotypes, including genomic rearrangements encompassing copies of Bna.FLC, Bna.PHYA and Bna.GA3ox1. De novo variation in copies of important flowering-time genes in B. napus arose during allopolyploidisation, enabling sub-functionalisation that allowed different morphotypes to appropriately fine-tune their lifecycle. |
format | Online Article Text |
id | pubmed-5292959 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-52929592017-02-10 Post-polyploidisation morphotype diversification associates with gene copy number variation Schiessl, Sarah Huettel, Bruno Kuehn, Diana Reinhardt, Richard Snowdon, Rod Sci Rep Article Genetic models for polyploid crop adaptation provide important information relevant for future breeding prospects. A well-suited model is Brassica napus, a recent allopolyploid closely related to Arabidopsis thaliana. Flowering time is a major adaptation trait determining life cycle synchronization with the environment. Here we unravel natural genetic variation in B. napus flowering time regulators and investigate associations with evolutionary diversification into different life cycle morphotypes. Deep sequencing of 35 flowering regulators was performed in 280 diverse B. napus genotypes. High sequencing depth enabled high-quality calling of single-nucleotide polymorphisms (SNPs), insertion-deletions (InDels) and copy number variants (CNVs). By combining these data with genotyping data from the Brassica 60 K Illumina® Infinium SNP array, we performed a genome-wide marker distribution analysis across the 4 ecogeographical morphotypes. Twelve haplotypes, including Bna.FLC.A10, Bna.VIN3.A02 and the Bna.FT promoter on C02_random, were diagnostic for the diversification of winter and spring types. The subspecies split between oilseed/kale (B. napus ssp. napus) and swedes/rutabagas (B. napus ssp. napobrassica) was defined by 13 haplotypes, including genomic rearrangements encompassing copies of Bna.FLC, Bna.PHYA and Bna.GA3ox1. De novo variation in copies of important flowering-time genes in B. napus arose during allopolyploidisation, enabling sub-functionalisation that allowed different morphotypes to appropriately fine-tune their lifecycle. Nature Publishing Group 2017-02-06 /pmc/articles/PMC5292959/ /pubmed/28165502 http://dx.doi.org/10.1038/srep41845 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Schiessl, Sarah Huettel, Bruno Kuehn, Diana Reinhardt, Richard Snowdon, Rod Post-polyploidisation morphotype diversification associates with gene copy number variation |
title | Post-polyploidisation morphotype diversification associates with gene copy number variation |
title_full | Post-polyploidisation morphotype diversification associates with gene copy number variation |
title_fullStr | Post-polyploidisation morphotype diversification associates with gene copy number variation |
title_full_unstemmed | Post-polyploidisation morphotype diversification associates with gene copy number variation |
title_short | Post-polyploidisation morphotype diversification associates with gene copy number variation |
title_sort | post-polyploidisation morphotype diversification associates with gene copy number variation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292959/ https://www.ncbi.nlm.nih.gov/pubmed/28165502 http://dx.doi.org/10.1038/srep41845 |
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