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A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication

BACKGROUND: Recent advancements in next-generation sequencing technology have enabled cost-effective sequencing of whole or partial genomes, permitting the discovery and characterization of molecular polymorphisms. Double-digest restriction-site associated DNA sequencing (ddRAD-seq) is a powerful an...

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Autores principales: Kai, Wataru, Nomura, Kazuharu, Fujiwara, Atushi, Nakamura, Yoji, Yasuike, Motoshige, Ojima, Nobuhiko, Masaoka, Tetsuji, Ozaki, Akiyuki, Kazeto, Yukinori, Gen, Koichiro, Nagao, Jiro, Tanaka, Hideki, Kobayashi, Takanori, Ototake, Mitsuru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986909/
https://www.ncbi.nlm.nih.gov/pubmed/24669946
http://dx.doi.org/10.1186/1471-2164-15-233
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author Kai, Wataru
Nomura, Kazuharu
Fujiwara, Atushi
Nakamura, Yoji
Yasuike, Motoshige
Ojima, Nobuhiko
Masaoka, Tetsuji
Ozaki, Akiyuki
Kazeto, Yukinori
Gen, Koichiro
Nagao, Jiro
Tanaka, Hideki
Kobayashi, Takanori
Ototake, Mitsuru
author_facet Kai, Wataru
Nomura, Kazuharu
Fujiwara, Atushi
Nakamura, Yoji
Yasuike, Motoshige
Ojima, Nobuhiko
Masaoka, Tetsuji
Ozaki, Akiyuki
Kazeto, Yukinori
Gen, Koichiro
Nagao, Jiro
Tanaka, Hideki
Kobayashi, Takanori
Ototake, Mitsuru
author_sort Kai, Wataru
collection PubMed
description BACKGROUND: Recent advancements in next-generation sequencing technology have enabled cost-effective sequencing of whole or partial genomes, permitting the discovery and characterization of molecular polymorphisms. Double-digest restriction-site associated DNA sequencing (ddRAD-seq) is a powerful and inexpensive approach to developing numerous single nucleotide polymorphism (SNP) markers and constructing a high-density genetic map. To enrich genomic resources for Japanese eel (Anguilla japonica), we constructed a ddRAD-based genetic map using an Ion Torrent Personal Genome Machine and anchored scaffolds of the current genome assembly to 19 linkage groups of the Japanese eel. Furthermore, we compared the Japanese eel genome with genomes of model fishes to infer the history of genome evolution after the teleost-specific genome duplication. RESULTS: We generated the ddRAD-based linkage map of the Japanese eel, where the maps for female and male spanned 1748.8 cM and 1294.5 cM, respectively, and were arranged into 19 linkage groups. A total of 2,672 SNP markers and 115 Simple Sequence Repeat markers provide anchor points to 1,252 scaffolds covering 151 Mb (13%) of the current genome assembly of the Japanese eel. Comparisons among the Japanese eel, medaka, zebrafish and spotted gar genomes showed highly conserved synteny among teleosts and revealed part of the eight major chromosomal rearrangement events that occurred soon after the teleost-specific genome duplication. CONCLUSIONS: The ddRAD-seq approach combined with the Ion Torrent Personal Genome Machine sequencing allowed us to conduct efficient and flexible SNP genotyping. The integration of the genetic map and the assembled sequence provides a valuable resource for fine mapping and positional cloning of quantitative trait loci associated with economically important traits and for investigating comparative genomics of the Japanese eel.
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spelling pubmed-39869092014-04-16 A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication Kai, Wataru Nomura, Kazuharu Fujiwara, Atushi Nakamura, Yoji Yasuike, Motoshige Ojima, Nobuhiko Masaoka, Tetsuji Ozaki, Akiyuki Kazeto, Yukinori Gen, Koichiro Nagao, Jiro Tanaka, Hideki Kobayashi, Takanori Ototake, Mitsuru BMC Genomics Research Article BACKGROUND: Recent advancements in next-generation sequencing technology have enabled cost-effective sequencing of whole or partial genomes, permitting the discovery and characterization of molecular polymorphisms. Double-digest restriction-site associated DNA sequencing (ddRAD-seq) is a powerful and inexpensive approach to developing numerous single nucleotide polymorphism (SNP) markers and constructing a high-density genetic map. To enrich genomic resources for Japanese eel (Anguilla japonica), we constructed a ddRAD-based genetic map using an Ion Torrent Personal Genome Machine and anchored scaffolds of the current genome assembly to 19 linkage groups of the Japanese eel. Furthermore, we compared the Japanese eel genome with genomes of model fishes to infer the history of genome evolution after the teleost-specific genome duplication. RESULTS: We generated the ddRAD-based linkage map of the Japanese eel, where the maps for female and male spanned 1748.8 cM and 1294.5 cM, respectively, and were arranged into 19 linkage groups. A total of 2,672 SNP markers and 115 Simple Sequence Repeat markers provide anchor points to 1,252 scaffolds covering 151 Mb (13%) of the current genome assembly of the Japanese eel. Comparisons among the Japanese eel, medaka, zebrafish and spotted gar genomes showed highly conserved synteny among teleosts and revealed part of the eight major chromosomal rearrangement events that occurred soon after the teleost-specific genome duplication. CONCLUSIONS: The ddRAD-seq approach combined with the Ion Torrent Personal Genome Machine sequencing allowed us to conduct efficient and flexible SNP genotyping. The integration of the genetic map and the assembled sequence provides a valuable resource for fine mapping and positional cloning of quantitative trait loci associated with economically important traits and for investigating comparative genomics of the Japanese eel. BioMed Central 2014-03-26 /pmc/articles/PMC3986909/ /pubmed/24669946 http://dx.doi.org/10.1186/1471-2164-15-233 Text en Copyright © 2014 Kai 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 credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Kai, Wataru
Nomura, Kazuharu
Fujiwara, Atushi
Nakamura, Yoji
Yasuike, Motoshige
Ojima, Nobuhiko
Masaoka, Tetsuji
Ozaki, Akiyuki
Kazeto, Yukinori
Gen, Koichiro
Nagao, Jiro
Tanaka, Hideki
Kobayashi, Takanori
Ototake, Mitsuru
A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication
title A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication
title_full A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication
title_fullStr A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication
title_full_unstemmed A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication
title_short A ddRAD-based genetic map and its integration with the genome assembly of Japanese eel (Anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication
title_sort ddrad-based genetic map and its integration with the genome assembly of japanese eel (anguilla japonica) provides insights into genome evolution after the teleost-specific genome duplication
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986909/
https://www.ncbi.nlm.nih.gov/pubmed/24669946
http://dx.doi.org/10.1186/1471-2164-15-233
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