A high-density SNP genotyping array for Brassica napus and its ancestral diploid species based on optimised selection of single-locus markers in the allotetraploid genome

Wayne E. Clarke(Agriculture and Agri-Food Canada), Erin E. Higgins(Agriculture and Agri-Food Canada), Joerg Plieske, Ralf Wieseke, Christine Sidebottom(National Research Council Canada), Yogendra Khedikar(Agriculture and Agri-Food Canada), Jacqueline Batley(The University of Western Australia), David Edwards(The University of Western Australia), Jinling Meng(Huazhong Agricultural University), Ruiyuan Li(Huazhong Agricultural University), Cindy Lawley(Illumina (United States)), Jérôme Pauquet(Syngenta (Switzerland)), Benjamin Laga(Bayer (Belgium)), Wing‐Yee Cheung, Federico Iñiguez-Luy(Agriaquaculture Nutritional Genomic Center), Emmanuelle Dyrszka, Stephen Rae(Bayer (Belgium)), Benjamin Stich(Max Planck Institute for Plant Breeding Research), Rod J. Snowdon(Justus-Liebig-Universität Gießen), Andrew Sharpe(National Research Council Canada), Martin W. Ganal, Isobel A. P. Parkin(Agriculture and Agri-Food Canada)
Theoretical and Applied Genetics
June 30, 2016
Cited by 249Open Access
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Abstract

KEY MESSAGE: The Brassica napus Illumina array provides genome-wide markers linked to the available genome sequence, a significant tool for genetic analyses of the allotetraploid B. napus and its progenitor diploid genomes. A high-density single nucleotide polymorphism (SNP) Illumina Infinium array, containing 52,157 markers, was developed for the allotetraploid Brassica napus. A stringent selection process employing the short probe sequence for each SNP assay was used to limit the majority of the selected markers to those represented a minimum number of times across the highly replicated genome. As a result approximately 60 % of the SNP assays display genome-specificity, resolving as three clearly separated clusters (AA, AB, and BB) when tested with a diverse range of B. napus material. This genome specificity was supported by the analysis of the diploid ancestors of B. napus, whereby 26,504 and 29,720 markers were scorable in B. oleracea and B. rapa, respectively. Forty-four percent of the assayed loci on the array were genetically mapped in a single doubled-haploid B. napus population allowing alignment of their physical and genetic coordinates. Although strong conservation of the two positions was shown, at least 3 % of the loci were genetically mapped to a homoeologous position compared to their presumed physical position in the respective genome, underlying the importance of genetic corroboration of locus identity. In addition, the alignments identified multiple rearrangements between the diploid and tetraploid Brassica genomes. Although mostly attributed to genome assembly errors, some are likely evidence of rearrangements that occurred since the hybridisation of the progenitor genomes in the B. napus nucleus. Based on estimates for linkage disequilibrium decay, the array is a valuable tool for genetic fine mapping and genome-wide association studies in B. napus and its progenitor genomes.


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