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Sex determination in the GIFT strain of tilapia is controlled by a locus in linkage group 23
BACKGROUND: Tilapias (Family Cichlidae) are the second most important group of aquaculture species in the world. They have been the subject of much research on sex determination due to problems caused by early maturation in culture and their complex sex-determining systems. Different sex-determining...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189693/ https://www.ncbi.nlm.nih.gov/pubmed/32349678 http://dx.doi.org/10.1186/s12863-020-00853-3 |
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author | Taslima, Khanam Wehner, Stefanie Taggart, John B. de Verdal, Hugues Benzie, John A. H. Bekaert, Michaël McAndrew, Brendan J. Penman, David J. |
author_facet | Taslima, Khanam Wehner, Stefanie Taggart, John B. de Verdal, Hugues Benzie, John A. H. Bekaert, Michaël McAndrew, Brendan J. Penman, David J. |
author_sort | Taslima, Khanam |
collection | PubMed |
description | BACKGROUND: Tilapias (Family Cichlidae) are the second most important group of aquaculture species in the world. They have been the subject of much research on sex determination due to problems caused by early maturation in culture and their complex sex-determining systems. Different sex-determining loci (linkage group 1, 20 and 23) have been detected in various tilapia stocks. The ‘genetically improved farmed tilapia’ (GIFT) stock, founded from multiple Nile tilapia (Oreochromis niloticus) populations, with some likely to have been introgressed with O. mossambicus, is a key resource for tilapia aquaculture. The sex-determining mechanism in the GIFT stock was unknown, but potentially complicated due to its multiple origins. RESULTS: A bulk segregant analysis (BSA) version of double-digest restriction-site associated DNA sequencing (BSA-ddRADseq) was developed and used to detect and position sex-linked single nucleotide polymorphism (SNP) markers in 19 families from the GIFT strain breeding nucleus and two Stirling families as controls (a single XY locus had been previously mapped to LG1 in the latter). About 1500 SNPs per family were detected across the genome. Phenotypic sex in Stirling families showed strong association with LG1, whereas only SNPs located in LG23 showed clear association with sex in the majority of the GIFT families. No other genomic regions linked to sex determination were apparent. This region was validated using a series of LG23-specific DNA markers (five SNPs with highest association to sex from this study, the LG23 sex-associated microsatellite UNH898 and ARO172, and the recently isolated amhy marker for individual fish (n = 284). CONCLUSIONS: Perhaps surprisingly given its multiple origins, sex determination in the GIFT strain breeding nucleus was associated only with a locus in LG23. BSA-ddRADseq allowed cost-effective analysis of multiple families, strengthening this conclusion. This technique has potential to be applied to other complex traits. The sex-linked SNP markers identified will be useful for potential marker-assisted selection (MAS) to control sex-ratio in GIFT tilapia to suppress unwanted reproduction during growout. |
format | Online Article Text |
id | pubmed-7189693 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-71896932020-05-04 Sex determination in the GIFT strain of tilapia is controlled by a locus in linkage group 23 Taslima, Khanam Wehner, Stefanie Taggart, John B. de Verdal, Hugues Benzie, John A. H. Bekaert, Michaël McAndrew, Brendan J. Penman, David J. BMC Genet Research Article BACKGROUND: Tilapias (Family Cichlidae) are the second most important group of aquaculture species in the world. They have been the subject of much research on sex determination due to problems caused by early maturation in culture and their complex sex-determining systems. Different sex-determining loci (linkage group 1, 20 and 23) have been detected in various tilapia stocks. The ‘genetically improved farmed tilapia’ (GIFT) stock, founded from multiple Nile tilapia (Oreochromis niloticus) populations, with some likely to have been introgressed with O. mossambicus, is a key resource for tilapia aquaculture. The sex-determining mechanism in the GIFT stock was unknown, but potentially complicated due to its multiple origins. RESULTS: A bulk segregant analysis (BSA) version of double-digest restriction-site associated DNA sequencing (BSA-ddRADseq) was developed and used to detect and position sex-linked single nucleotide polymorphism (SNP) markers in 19 families from the GIFT strain breeding nucleus and two Stirling families as controls (a single XY locus had been previously mapped to LG1 in the latter). About 1500 SNPs per family were detected across the genome. Phenotypic sex in Stirling families showed strong association with LG1, whereas only SNPs located in LG23 showed clear association with sex in the majority of the GIFT families. No other genomic regions linked to sex determination were apparent. This region was validated using a series of LG23-specific DNA markers (five SNPs with highest association to sex from this study, the LG23 sex-associated microsatellite UNH898 and ARO172, and the recently isolated amhy marker for individual fish (n = 284). CONCLUSIONS: Perhaps surprisingly given its multiple origins, sex determination in the GIFT strain breeding nucleus was associated only with a locus in LG23. BSA-ddRADseq allowed cost-effective analysis of multiple families, strengthening this conclusion. This technique has potential to be applied to other complex traits. The sex-linked SNP markers identified will be useful for potential marker-assisted selection (MAS) to control sex-ratio in GIFT tilapia to suppress unwanted reproduction during growout. BioMed Central 2020-04-29 /pmc/articles/PMC7189693/ /pubmed/32349678 http://dx.doi.org/10.1186/s12863-020-00853-3 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data. |
spellingShingle | Research Article Taslima, Khanam Wehner, Stefanie Taggart, John B. de Verdal, Hugues Benzie, John A. H. Bekaert, Michaël McAndrew, Brendan J. Penman, David J. Sex determination in the GIFT strain of tilapia is controlled by a locus in linkage group 23 |
title | Sex determination in the GIFT strain of tilapia is controlled by a locus in linkage group 23 |
title_full | Sex determination in the GIFT strain of tilapia is controlled by a locus in linkage group 23 |
title_fullStr | Sex determination in the GIFT strain of tilapia is controlled by a locus in linkage group 23 |
title_full_unstemmed | Sex determination in the GIFT strain of tilapia is controlled by a locus in linkage group 23 |
title_short | Sex determination in the GIFT strain of tilapia is controlled by a locus in linkage group 23 |
title_sort | sex determination in the gift strain of tilapia is controlled by a locus in linkage group 23 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7189693/ https://www.ncbi.nlm.nih.gov/pubmed/32349678 http://dx.doi.org/10.1186/s12863-020-00853-3 |
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