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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.

Identifieur interne : 002429 ( PubMed/Checkpoint ); précédent : 002428; suivant : 002430

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.

Auteurs : Wayne E. Clarke [Canada] ; Erin E. Higgins [Canada] ; Joerg Plieske [Allemagne] ; Ralf Wieseke [Allemagne] ; Christine Sidebottom [Canada] ; Yogendra Khedikar [Canada] ; Jacqueline Batley [Australie] ; Dave Edwards [Australie] ; Jinling Meng [République populaire de Chine] ; Ruiyuan Li [République populaire de Chine] ; Cynthia Taylor Lawley [États-Unis] ; Jérôme Pauquet [France] ; Benjamin Laga [Belgique] ; Wing Cheung [Canada] ; Federico Iniguez-Luy [Chili] ; Emmanuelle Dyrszka [France] ; Stephen Rae [Belgique] ; Benjamin Stich [Allemagne] ; Rod J. Snowdon [Allemagne] ; Andrew G. Sharpe [Canada] ; Martin W. Ganal [Allemagne] ; Isobel A P. Parkin [Canada]

Source :

RBID : pubmed:27364915

Descripteurs français

English descriptors

Abstract

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.

DOI: 10.1007/s00122-016-2746-7
PubMed: 27364915


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<name sortKey="Cheung, Wing" sort="Cheung, Wing" uniqKey="Cheung W" first="Wing" last="Cheung">Wing Cheung</name>
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<name sortKey="Iniguez Luy, Federico" sort="Iniguez Luy, Federico" uniqKey="Iniguez Luy F" first="Federico" last="Iniguez-Luy">Federico Iniguez-Luy</name>
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<name sortKey="Snowdon, Rod J" sort="Snowdon, Rod J" uniqKey="Snowdon R" first="Rod J" last="Snowdon">Rod J. Snowdon</name>
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<name sortKey="Ganal, Martin W" sort="Ganal, Martin W" uniqKey="Ganal M" first="Martin W" last="Ganal">Martin W. Ganal</name>
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<name sortKey="Parkin, Isobel A P" sort="Parkin, Isobel A P" uniqKey="Parkin I" first="Isobel A P" last="Parkin">Isobel A P. Parkin</name>
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<name sortKey="Sidebottom, Christine" sort="Sidebottom, Christine" uniqKey="Sidebottom C" first="Christine" last="Sidebottom">Christine Sidebottom</name>
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<name sortKey="Khedikar, Yogendra" sort="Khedikar, Yogendra" uniqKey="Khedikar Y" first="Yogendra" last="Khedikar">Yogendra Khedikar</name>
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<name sortKey="Batley, Jacqueline" sort="Batley, Jacqueline" uniqKey="Batley J" first="Jacqueline" last="Batley">Jacqueline Batley</name>
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<nlm:affiliation>School of Plant Biology and The UWA Institute of Agriculture, The University of Western Australia, 35 Stirling Highway, Crawley, Perth, 6009, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
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<name sortKey="Edwards, Dave" sort="Edwards, Dave" uniqKey="Edwards D" first="Dave" last="Edwards">Dave Edwards</name>
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<nlm:affiliation>School of Plant Biology and The UWA Institute of Agriculture, The University of Western Australia, 35 Stirling Highway, Crawley, Perth, 6009, Australia.</nlm:affiliation>
<country xml:lang="fr">Australie</country>
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<name sortKey="Meng, Jinling" sort="Meng, Jinling" uniqKey="Meng J" first="Jinling" last="Meng">Jinling Meng</name>
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<nlm:affiliation>National Key Laboratory of Crop Genetic Improvement, Key Laboratory of Rapeseed Genetic Improvement, Ministry of Agriculture P. R. China, Huazhong Agricultural University, Wuhan, 430070, China.</nlm:affiliation>
<country xml:lang="fr">République populaire de Chine</country>
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<name sortKey="Li, Ruiyuan" sort="Li, Ruiyuan" uniqKey="Li R" first="Ruiyuan" last="Li">Ruiyuan Li</name>
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<name sortKey="Parkin, Isobel A P" sort="Parkin, Isobel A P" uniqKey="Parkin I" first="Isobel A P" last="Parkin">Isobel A P. Parkin</name>
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<title level="j">TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik</title>
<idno type="eISSN">1432-2242</idno>
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<term>Brassica napus (genetics)</term>
<term>Chromosome Mapping</term>
<term>DNA, Plant (genetics)</term>
<term>Diploidy</term>
<term>Genetic Markers</term>
<term>Genome, Plant</term>
<term>Genotyping Techniques</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Sequence Analysis, DNA</term>
<term>Tetraploidy</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>ADN des plantes (génétique)</term>
<term>Analyse de séquence d'ADN</term>
<term>Brassica napus (génétique)</term>
<term>Cartographie chromosomique</term>
<term>Diploïdie</term>
<term>Génome végétal</term>
<term>Marqueurs génétiques</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Techniques de génotypage</term>
<term>Tétraploïdie</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>DNA, Plant</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>Brassica napus</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>ADN des plantes</term>
<term>Brassica napus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Chromosome Mapping</term>
<term>Diploidy</term>
<term>Genetic Markers</term>
<term>Genome, Plant</term>
<term>Genotyping Techniques</term>
<term>Polymorphism, Single Nucleotide</term>
<term>Sequence Analysis, DNA</term>
<term>Tetraploidy</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse de séquence d'ADN</term>
<term>Cartographie chromosomique</term>
<term>Diploïdie</term>
<term>Génome végétal</term>
<term>Marqueurs génétiques</term>
<term>Polymorphisme de nucléotide simple</term>
<term>Techniques de génotypage</term>
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<div type="abstract" xml:lang="en">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.</div>
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<Year>2016</Year>
<Month>09</Month>
<Day>17</Day>
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<DateCompleted>
<Year>2017</Year>
<Month>01</Month>
<Day>05</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>02</Month>
<Day>24</Day>
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<ISSN IssnType="Electronic">1432-2242</ISSN>
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<Volume>129</Volume>
<Issue>10</Issue>
<PubDate>
<Year>2016</Year>
<Month>Oct</Month>
</PubDate>
</JournalIssue>
<Title>TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik</Title>
<ISOAbbreviation>Theor. Appl. Genet.</ISOAbbreviation>
</Journal>
<ArticleTitle>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.</ArticleTitle>
<Pagination>
<MedlinePgn>1887-99</MedlinePgn>
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<ELocationID EIdType="doi" ValidYN="Y">10.1007/s00122-016-2746-7</ELocationID>
<Abstract>
<AbstractText Label="KEY MESSAGE" NlmCategory="CONCLUSIONS">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.</AbstractText>
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<ForeName>Jinling</ForeName>
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<AffiliationInfo>
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<MeshHeadingList>
<MeshHeading>
<DescriptorName UI="D029688" MajorTopicYN="N">Brassica napus</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="Y">genetics</QualifierName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D002874" MajorTopicYN="Y">Chromosome Mapping</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D018744" MajorTopicYN="N">DNA, Plant</DescriptorName>
<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
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<MeshHeading>
<DescriptorName UI="D004171" MajorTopicYN="N">Diploidy</DescriptorName>
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<MeshHeading>
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<MeshHeading>
<DescriptorName UI="D060005" MajorTopicYN="Y">Genotyping Techniques</DescriptorName>
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<MeshHeading>
<DescriptorName UI="D020641" MajorTopicYN="Y">Polymorphism, Single Nucleotide</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D017422" MajorTopicYN="N">Sequence Analysis, DNA</DescriptorName>
</MeshHeading>
<MeshHeading>
<DescriptorName UI="D057891" MajorTopicYN="N">Tetraploidy</DescriptorName>
</MeshHeading>
</MeshHeadingList>
<CoiStatement>The authors MWG, RW, and JP have competing commercial interests as members of TraitGenetics GmbH which is a company that offers marker development and analysis (including this array) for commercial purposes. This does not alter the authors’ adherence to sharing data.</CoiStatement>
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<Year>2016</Year>
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<ArticleId IdType="doi">10.1007/s00122-016-2746-7</ArticleId>
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