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Construction of a reference genetic linkage map for carnation (Dianthus caryophyllus L.)

BACKGROUND: Genetic linkage maps are important tools for many genetic applications including mapping of quantitative trait loci (QTLs), identifying DNA markers for fingerprinting, and map-based gene cloning. Carnation (Dianthus caryophyllus L.) is an important ornamental flower worldwide. We previou...

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Autores principales: Yagi, Masafumi, Yamamoto, Toshiya, Isobe, Sachiko, Hirakawa, Hideki, Tabata, Satoshi, Tanase, Koji, Yamaguchi, Hiroyasu, Onozaki, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870981/
https://www.ncbi.nlm.nih.gov/pubmed/24160306
http://dx.doi.org/10.1186/1471-2164-14-734
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author Yagi, Masafumi
Yamamoto, Toshiya
Isobe, Sachiko
Hirakawa, Hideki
Tabata, Satoshi
Tanase, Koji
Yamaguchi, Hiroyasu
Onozaki, Takashi
author_facet Yagi, Masafumi
Yamamoto, Toshiya
Isobe, Sachiko
Hirakawa, Hideki
Tabata, Satoshi
Tanase, Koji
Yamaguchi, Hiroyasu
Onozaki, Takashi
author_sort Yagi, Masafumi
collection PubMed
description BACKGROUND: Genetic linkage maps are important tools for many genetic applications including mapping of quantitative trait loci (QTLs), identifying DNA markers for fingerprinting, and map-based gene cloning. Carnation (Dianthus caryophyllus L.) is an important ornamental flower worldwide. We previously reported a random amplified polymorphic DNA (RAPD)-based genetic linkage map derived from Dianthus capitatus ssp. andrezejowskianus and a simple sequence repeat (SSR)-based genetic linkage map constructed using data from intraspecific F(2) populations; however, the number of markers was insufficient, and so the number of linkage groups (LGs) did not coincide with the number of chromosomes (x = 15). Therefore, we aimed to produce a high-density genetic map to improve its usefulness for breeding purposes and genetic research. RESULTS: We improved the SSR-based genetic linkage map using SSR markers derived from a genomic library, expression sequence tags, and RNA-seq data. Linkage analysis revealed that 412 SSR loci (including 234 newly developed SSR loci) could be mapped to 17 linkage groups (LGs) covering 969.6 cM. Comparison of five minor LGs covering less than 50 cM with LGs in our previous RAPD-based genetic map suggested that four LGs could be integrated into two LGs by anchoring common SSR loci. Consequently, the number of LGs corresponded to the number of chromosomes (x = 15). We added 192 new SSRs, eight RAPD, and two sequence-tagged site loci to refine the RAPD-based genetic linkage map, which comprised 15 LGs consisting of 348 loci covering 978.3 cM. The two maps had 125 SSR loci in common, and most of the positions of markers were conserved between them. We identified 635 loci in carnation using the two linkage maps. We also mapped QTLs for two traits (bacterial wilt resistance and anthocyanin pigmentation in the flower) and a phenotypic locus for flower-type by analyzing previously reported genotype and phenotype data. CONCLUSIONS: The improved genetic linkage maps and SSR markers developed in this study will serve as reference genetic linkage maps for members of the genus Dianthus, including carnation, and will be useful for mapping QTLs associated with various traits, and for improving carnation breeding programs.
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spelling pubmed-38709812013-12-25 Construction of a reference genetic linkage map for carnation (Dianthus caryophyllus L.) Yagi, Masafumi Yamamoto, Toshiya Isobe, Sachiko Hirakawa, Hideki Tabata, Satoshi Tanase, Koji Yamaguchi, Hiroyasu Onozaki, Takashi BMC Genomics Research Article BACKGROUND: Genetic linkage maps are important tools for many genetic applications including mapping of quantitative trait loci (QTLs), identifying DNA markers for fingerprinting, and map-based gene cloning. Carnation (Dianthus caryophyllus L.) is an important ornamental flower worldwide. We previously reported a random amplified polymorphic DNA (RAPD)-based genetic linkage map derived from Dianthus capitatus ssp. andrezejowskianus and a simple sequence repeat (SSR)-based genetic linkage map constructed using data from intraspecific F(2) populations; however, the number of markers was insufficient, and so the number of linkage groups (LGs) did not coincide with the number of chromosomes (x = 15). Therefore, we aimed to produce a high-density genetic map to improve its usefulness for breeding purposes and genetic research. RESULTS: We improved the SSR-based genetic linkage map using SSR markers derived from a genomic library, expression sequence tags, and RNA-seq data. Linkage analysis revealed that 412 SSR loci (including 234 newly developed SSR loci) could be mapped to 17 linkage groups (LGs) covering 969.6 cM. Comparison of five minor LGs covering less than 50 cM with LGs in our previous RAPD-based genetic map suggested that four LGs could be integrated into two LGs by anchoring common SSR loci. Consequently, the number of LGs corresponded to the number of chromosomes (x = 15). We added 192 new SSRs, eight RAPD, and two sequence-tagged site loci to refine the RAPD-based genetic linkage map, which comprised 15 LGs consisting of 348 loci covering 978.3 cM. The two maps had 125 SSR loci in common, and most of the positions of markers were conserved between them. We identified 635 loci in carnation using the two linkage maps. We also mapped QTLs for two traits (bacterial wilt resistance and anthocyanin pigmentation in the flower) and a phenotypic locus for flower-type by analyzing previously reported genotype and phenotype data. CONCLUSIONS: The improved genetic linkage maps and SSR markers developed in this study will serve as reference genetic linkage maps for members of the genus Dianthus, including carnation, and will be useful for mapping QTLs associated with various traits, and for improving carnation breeding programs. BioMed Central 2013-10-26 /pmc/articles/PMC3870981/ /pubmed/24160306 http://dx.doi.org/10.1186/1471-2164-14-734 Text en Copyright © 2013 Yagi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yagi, Masafumi
Yamamoto, Toshiya
Isobe, Sachiko
Hirakawa, Hideki
Tabata, Satoshi
Tanase, Koji
Yamaguchi, Hiroyasu
Onozaki, Takashi
Construction of a reference genetic linkage map for carnation (Dianthus caryophyllus L.)
title Construction of a reference genetic linkage map for carnation (Dianthus caryophyllus L.)
title_full Construction of a reference genetic linkage map for carnation (Dianthus caryophyllus L.)
title_fullStr Construction of a reference genetic linkage map for carnation (Dianthus caryophyllus L.)
title_full_unstemmed Construction of a reference genetic linkage map for carnation (Dianthus caryophyllus L.)
title_short Construction of a reference genetic linkage map for carnation (Dianthus caryophyllus L.)
title_sort construction of a reference genetic linkage map for carnation (dianthus caryophyllus l.)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3870981/
https://www.ncbi.nlm.nih.gov/pubmed/24160306
http://dx.doi.org/10.1186/1471-2164-14-734
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