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Improvement of the Pacific bluefin tuna (Thunnus orientalis) reference genome and development of male-specific DNA markers
by
Suzuki, Nobuaki
, Matsuura, Aiko
, Nishiki, Issei
, Akita, Tetsuya
, Fujiwara, Atushi
, Suda, Ayako
, Iwasaki, Yuki
in
45/43
/ 631/208/205/2138
/ 631/208/721
/ Animals
/ Deoxyribonucleic acid
/ DNA
/ Farms
/ Female
/ Genetic Markers
/ Genome
/ Genomes
/ Gonads
/ Growth rate
/ Humanities and Social Sciences
/ Linkage disequilibrium
/ Male
/ Males
/ Migratory species
/ multidisciplinary
/ Natural populations
/ Nucleotide sequence
/ Pacific Ocean
/ Polymerase chain reaction
/ Polymerase Chain Reaction - veterinary
/ Primers
/ Science
/ Science (multidisciplinary)
/ Sex determination
/ Sex Determination Analysis - methods
/ Sex Determination Analysis - veterinary
/ Sex Determination Processes
/ Sex ratio
/ Sexual dimorphism
/ Single-nucleotide polymorphism
/ Thunnus orientalis
/ Tuna
/ Tuna - genetics
/ Whole Genome Sequencing - veterinary
2019
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Improvement of the Pacific bluefin tuna (Thunnus orientalis) reference genome and development of male-specific DNA markers
by
Suzuki, Nobuaki
, Matsuura, Aiko
, Nishiki, Issei
, Akita, Tetsuya
, Fujiwara, Atushi
, Suda, Ayako
, Iwasaki, Yuki
in
45/43
/ 631/208/205/2138
/ 631/208/721
/ Animals
/ Deoxyribonucleic acid
/ DNA
/ Farms
/ Female
/ Genetic Markers
/ Genome
/ Genomes
/ Gonads
/ Growth rate
/ Humanities and Social Sciences
/ Linkage disequilibrium
/ Male
/ Males
/ Migratory species
/ multidisciplinary
/ Natural populations
/ Nucleotide sequence
/ Pacific Ocean
/ Polymerase chain reaction
/ Polymerase Chain Reaction - veterinary
/ Primers
/ Science
/ Science (multidisciplinary)
/ Sex determination
/ Sex Determination Analysis - methods
/ Sex Determination Analysis - veterinary
/ Sex Determination Processes
/ Sex ratio
/ Sexual dimorphism
/ Single-nucleotide polymorphism
/ Thunnus orientalis
/ Tuna
/ Tuna - genetics
/ Whole Genome Sequencing - veterinary
2019
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Improvement of the Pacific bluefin tuna (Thunnus orientalis) reference genome and development of male-specific DNA markers
by
Suzuki, Nobuaki
, Matsuura, Aiko
, Nishiki, Issei
, Akita, Tetsuya
, Fujiwara, Atushi
, Suda, Ayako
, Iwasaki, Yuki
in
45/43
/ 631/208/205/2138
/ 631/208/721
/ Animals
/ Deoxyribonucleic acid
/ DNA
/ Farms
/ Female
/ Genetic Markers
/ Genome
/ Genomes
/ Gonads
/ Growth rate
/ Humanities and Social Sciences
/ Linkage disequilibrium
/ Male
/ Males
/ Migratory species
/ multidisciplinary
/ Natural populations
/ Nucleotide sequence
/ Pacific Ocean
/ Polymerase chain reaction
/ Polymerase Chain Reaction - veterinary
/ Primers
/ Science
/ Science (multidisciplinary)
/ Sex determination
/ Sex Determination Analysis - methods
/ Sex Determination Analysis - veterinary
/ Sex Determination Processes
/ Sex ratio
/ Sexual dimorphism
/ Single-nucleotide polymorphism
/ Thunnus orientalis
/ Tuna
/ Tuna - genetics
/ Whole Genome Sequencing - veterinary
2019
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Improvement of the Pacific bluefin tuna (Thunnus orientalis) reference genome and development of male-specific DNA markers
Journal Article
Improvement of the Pacific bluefin tuna (Thunnus orientalis) reference genome and development of male-specific DNA markers
2019
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Overview
The Pacific bluefin tuna,
Thunnus orientalis
, is a highly migratory species that is widely distributed in the North Pacific Ocean. Like other marine species,
T. orientalis
has no external sexual dimorphism; thus, identifying sex-specific variants from whole genome sequence data is a useful approach to develop an effective sex identification method. Here, we report an improved draft genome of
T. orientalis
and male-specific DNA markers. Combining PacBio long reads and Illumina short reads sufficiently improved genome assembly, with a 38-fold increase in scaffold contiguity (to 444 scaffolds) compared to the first published draft genome. Through analysing re-sequence data of 15 males and 16 females, 250 male-specific SNPs were identified from more than 30 million polymorphisms. All male-specific variants were male-heterozygous, suggesting that
T. orientalis
has a male heterogametic sex-determination system. The largest linkage disequilibrium block (3,174 bp on scaffold_064) contained 51 male-specific variants. PCR primers and a PCR-based sex identification assay were developed using these male-specific variants. The sex of 115 individuals (56 males and 59 females; sex was diagnosed by visual examination of the gonads) was identified with high accuracy using the assay. This easy, accurate, and practical technique facilitates the control of sex ratios in tuna farms. Furthermore, this method could be used to estimate the sex ratio and/or the sex-specific growth rate of natural populations.
Publisher
Nature Publishing Group UK,Nature Publishing Group
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