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Co-linearity and divergence of the A subgenome of Brassica juncea compared with other Brassica species carrying different A subgenomes.

Identifieur interne : 002339 ( PubMed/Curation ); précédent : 002338; suivant : 002340

Co-linearity and divergence of the A subgenome of Brassica juncea compared with other Brassica species carrying different A subgenomes.

Auteurs : Jun Zou [République populaire de Chine] ; Dandan Hu [République populaire de Chine] ; Peifa Liu [République populaire de Chine] ; Harsh Raman [Australie] ; Zhongsong Liu [République populaire de Chine] ; Xianjun Liu [République populaire de Chine] ; Isobel A P. Parkin [Canada] ; Boulos Chalhoub [France] ; Jinling Meng [République populaire de Chine]

Source :

RBID : pubmed:26728943

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English descriptors

Abstract

There are three basic Brassica genomes (A, B, and C) and three parallel sets of subgenomes distinguished in the diploid Brassica (i.e.: B. rapa, A(r)A(r); B. nigra, B(ni)B(ni); B. oleracea, C(o)C(o)) and the derived allotetraploid species (i.e.: B. juncea, A(j)A(j)B(j)B(j); B. napus, A(n)A(n)C(n)C(n); B. carinata, B(c)B(c)C(c)C(c)). To understand subgenome differentiation in B. juncea in comparison to other A genome-carrying Brassica species (B. rapa and B. napus), we constructed a dense genetic linkage map of B. juncea, and conducted population genetic analysis on diverse lines of the three A-genome carrying Brassica species using a genotyping-by-sequencing approach (DArT-seq).

DOI: 10.1186/s12864-015-2343-1
PubMed: 26728943

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pubmed:26728943

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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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<term>Arabidopsis (genetics)</term>
<term>Brassica napus (genetics)</term>
<term>Chromosome Mapping</term>
<term>Diploidy</term>
<term>Genetic Linkage</term>
<term>Genome, Plant (genetics)</term>
<term>Genotype</term>
<term>Microsatellite Repeats (genetics)</term>
<term>Mustard Plant (genetics)</term>
<term>Quantitative Trait Loci (genetics)</term>
<term>Sequence Analysis, DNA</term>
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<term>Analyse de séquence d'ADN</term>
<term>Arabidopsis (génétique)</term>
<term>Brassica napus (génétique)</term>
<term>Cartographie chromosomique</term>
<term>Diploïdie</term>
<term>Génome végétal (génétique)</term>
<term>Génotype</term>
<term>Liaison génétique</term>
<term>Locus de caractère quantitatif (génétique)</term>
<term>Moutarde (plante) (génétique)</term>
<term>Répétitions microsatellites (génétique)</term>
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<term>Arabidopsis</term>
<term>Brassica napus</term>
<term>Genome, Plant</term>
<term>Microsatellite Repeats</term>
<term>Mustard Plant</term>
<term>Quantitative Trait Loci</term>
</keywords>
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<term>Arabidopsis</term>
<term>Brassica napus</term>
<term>Génome végétal</term>
<term>Locus de caractère quantitatif</term>
<term>Moutarde (plante)</term>
<term>Répétitions microsatellites</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Chromosome Mapping</term>
<term>Diploidy</term>
<term>Genetic Linkage</term>
<term>Genotype</term>
<term>Sequence Analysis, DNA</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse de séquence d'ADN</term>
<term>Cartographie chromosomique</term>
<term>Diploïdie</term>
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<div type="abstract" xml:lang="en">There are three basic Brassica genomes (A, B, and C) and three parallel sets of subgenomes distinguished in the diploid Brassica (i.e.: B. rapa, A(r)A(r); B. nigra, B(ni)B(ni); B. oleracea, C(o)C(o)) and the derived allotetraploid species (i.e.: B. juncea, A(j)A(j)B(j)B(j); B. napus, A(n)A(n)C(n)C(n); B. carinata, B(c)B(c)C(c)C(c)). To understand subgenome differentiation in B. juncea in comparison to other A genome-carrying Brassica species (B. rapa and B. napus), we constructed a dense genetic linkage map of B. juncea, and conducted population genetic analysis on diverse lines of the three A-genome carrying Brassica species using a genotyping-by-sequencing approach (DArT-seq).</div>
</front>
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<DateCreated>
<Year>2016</Year>
<Month>01</Month>
<Day>05</Day>
</DateCreated>
<DateCompleted>
<Year>2016</Year>
<Month>09</Month>
<Day>28</Day>
</DateCompleted>
<DateRevised>
<Year>2017</Year>
<Month>02</Month>
<Day>20</Day>
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<ISSN IssnType="Electronic">1471-2164</ISSN>
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<Volume>17</Volume>
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<Year>2016</Year>
<Month>Jan</Month>
<Day>05</Day>
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<Title>BMC genomics</Title>
<ISOAbbreviation>BMC Genomics</ISOAbbreviation>
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<ArticleTitle>Co-linearity and divergence of the A subgenome of Brassica juncea compared with other Brassica species carrying different A subgenomes.</ArticleTitle>
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<Abstract>
<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">There are three basic Brassica genomes (A, B, and C) and three parallel sets of subgenomes distinguished in the diploid Brassica (i.e.: B. rapa, A(r)A(r); B. nigra, B(ni)B(ni); B. oleracea, C(o)C(o)) and the derived allotetraploid species (i.e.: B. juncea, A(j)A(j)B(j)B(j); B. napus, A(n)A(n)C(n)C(n); B. carinata, B(c)B(c)C(c)C(c)). To understand subgenome differentiation in B. juncea in comparison to other A genome-carrying Brassica species (B. rapa and B. napus), we constructed a dense genetic linkage map of B. juncea, and conducted population genetic analysis on diverse lines of the three A-genome carrying Brassica species using a genotyping-by-sequencing approach (DArT-seq).</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">A dense genetic linkage map of B. juncea was constructed using an F2 population derived from Sichuan Yellow/Purple Mustard. The map included 3329 DArT-seq markers on 18 linkage groups and covered 1579 cM with an average density of two markers per cM. Based on this map and the alignment of the marker sequences with the physical genome of Arabidopsis thaliana, we observed strong co-linearity of the ancestral blocks among the different A subgenomes but also considerable block variation. Comparative analyses at the level of genome sequences of B. rapa and B. napus, and marker sequence anchored on the genetic map of B. juncea, revealed a total of 30 potential inversion events across large segments and 20 potential translocation events among the three A subgenomes. Population genetic analysis on 26 accessions of the three A genome-carrying Brassica species showed that the highest genetic distance were estimated when comparing A(j)-A(n) than between A(n)-A(r) and A(j)-A(r) subgenome pairs.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">The development of the dense genetic linkage map of B. juncea with informative DArT-seq marker sequences and availability of the reference sequences of the A(r), and A(n)C(n) genomes allowed us to compare the A subgenome structure of B. juncea (A(j)) . Our results suggest that strong co-linearity exists among the three A Brassica genomes (A(r), A(n) and A(j)) but with apparent subgenomic variation. Population genetic analysis on three A-genome carrying Brassica species support the idea that B. juncea has distinct genomic diversity, and/or evolved from a different A genome progenitor of B. napus.</AbstractText>
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<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. daist82@163.com.</Affiliation>
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<Affiliation>Graham Centre for Agricultural Innovation (an alliance between the Charles Sturt University and NSW Department of Primary Industries), Wagga Wagga Agricultural Institute, Wagga Wagga, NSW, 2650, Australia. harsh.raman@dpi.nsw.gov.au.</Affiliation>
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<Affiliation>Oilseed Crops Institute, Hunan Agricultural University, Changsha, 410128, China. zsliu48@sohu.com.</Affiliation>
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<LastName>Liu</LastName>
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<Affiliation>Oilseed Crops Institute, Hunan Agricultural University, Changsha, 410128, China. lxxjjz@sina.com.</Affiliation>
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<LastName>Meng</LastName>
<ForeName>Jinling</ForeName>
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