Identification of the major sex-determining region of turbot (Scophthalmus maximus)

17 p., 3 tables, 4 figures and bibliography Sex determination in fish is a labile character in evolutionary terms. The sex-determining (SD) master gene can differ even between closely related fish species. This group is an interesting model for studying the evolution of the SD region and the gonadal...

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Published in:Genetics
Main Authors: Felip, Alicia, Piferrer, Francesc
Format: Article in Journal/Newspaper
Language:English
Published: Genetics Society of America 2009
Subjects:
Online Access:http://hdl.handle.net/10261/47391
https://doi.org/10.1534/genetics.109.107979
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spelling ftcsic:oai:digital.csic.es:10261/47391 2024-02-11T10:08:26+01:00 Identification of the major sex-determining region of turbot (Scophthalmus maximus) Felip, Alicia Piferrer, Francesc 2009-12 http://hdl.handle.net/10261/47391 https://doi.org/10.1534/genetics.109.107979 en eng Genetics Society of America http://dx.doi.org/10.1534/genetics.109.107979 Genetics 183(4): 1443-1452 (2009) 0016-6731 http://hdl.handle.net/10261/47391 doi:10.1534/genetics.109.107979 1943-2631 19786621 none artículo http://purl.org/coar/resource_type/c_6501 2009 ftcsic https://doi.org/10.1534/genetics.109.107979 2024-01-16T09:36:49Z 17 p., 3 tables, 4 figures and bibliography Sex determination in fish is a labile character in evolutionary terms. The sex-determining (SD) master gene can differ even between closely related fish species. This group is an interesting model for studying the evolution of the SD region and the gonadal differentiation pathway. The turbot (Scophthalmus maximus) is a flatfish of great commercial value, where a strong sexual dimorphism exists for growth rate. Following a QTL and marker association approach in five families and a natural population, we identified the main SD region of turbot at the proximal end of linkage group (LG) 5, close to the SmaUSC-E30 marker. The refined map of this region suggested that this marker would be 2.6 cM and 1.4 Mb from the putative SD gene. This region appeared mostly undifferentiated between males and females, and no relevant recombination frequency differences were detected between sexes. Comparative genomics of LG5 marker sequences against five model species showed no similarity of this chromosome to the sex chromosomes of medaka, stickleback, and fugu, but suggested a similarity to a sex-associated QTL from Oreochromis spp. The segregation analysis of the closest markers to the SD region demonstrated a ZW/ZZ model of sex determination in turbot. A small proportion of families did not fit perfectly with this model, which suggests that other minor genetic and/or environmental factors are involved in sex determination in this species. This study was supported by the Consellería de Pesca e Asuntos Marítimos and the Dirección Xeral de I1D-Xunta de Galicia project (2004/CP480) and by the Spanish government (Consolider Ingenio Aquagenomics: CSD200700002) project. Peer reviewed Article in Journal/Newspaper Scophthalmus maximus Turbot Digital.CSIC (Spanish National Research Council) Genetics 183 4 1443 1452
institution Open Polar
collection Digital.CSIC (Spanish National Research Council)
op_collection_id ftcsic
language English
description 17 p., 3 tables, 4 figures and bibliography Sex determination in fish is a labile character in evolutionary terms. The sex-determining (SD) master gene can differ even between closely related fish species. This group is an interesting model for studying the evolution of the SD region and the gonadal differentiation pathway. The turbot (Scophthalmus maximus) is a flatfish of great commercial value, where a strong sexual dimorphism exists for growth rate. Following a QTL and marker association approach in five families and a natural population, we identified the main SD region of turbot at the proximal end of linkage group (LG) 5, close to the SmaUSC-E30 marker. The refined map of this region suggested that this marker would be 2.6 cM and 1.4 Mb from the putative SD gene. This region appeared mostly undifferentiated between males and females, and no relevant recombination frequency differences were detected between sexes. Comparative genomics of LG5 marker sequences against five model species showed no similarity of this chromosome to the sex chromosomes of medaka, stickleback, and fugu, but suggested a similarity to a sex-associated QTL from Oreochromis spp. The segregation analysis of the closest markers to the SD region demonstrated a ZW/ZZ model of sex determination in turbot. A small proportion of families did not fit perfectly with this model, which suggests that other minor genetic and/or environmental factors are involved in sex determination in this species. This study was supported by the Consellería de Pesca e Asuntos Marítimos and the Dirección Xeral de I1D-Xunta de Galicia project (2004/CP480) and by the Spanish government (Consolider Ingenio Aquagenomics: CSD200700002) project. Peer reviewed
format Article in Journal/Newspaper
author Felip, Alicia
Piferrer, Francesc
spellingShingle Felip, Alicia
Piferrer, Francesc
Identification of the major sex-determining region of turbot (Scophthalmus maximus)
author_facet Felip, Alicia
Piferrer, Francesc
author_sort Felip, Alicia
title Identification of the major sex-determining region of turbot (Scophthalmus maximus)
title_short Identification of the major sex-determining region of turbot (Scophthalmus maximus)
title_full Identification of the major sex-determining region of turbot (Scophthalmus maximus)
title_fullStr Identification of the major sex-determining region of turbot (Scophthalmus maximus)
title_full_unstemmed Identification of the major sex-determining region of turbot (Scophthalmus maximus)
title_sort identification of the major sex-determining region of turbot (scophthalmus maximus)
publisher Genetics Society of America
publishDate 2009
url http://hdl.handle.net/10261/47391
https://doi.org/10.1534/genetics.109.107979
genre Scophthalmus maximus
Turbot
genre_facet Scophthalmus maximus
Turbot
op_relation http://dx.doi.org/10.1534/genetics.109.107979
Genetics 183(4): 1443-1452 (2009)
0016-6731
http://hdl.handle.net/10261/47391
doi:10.1534/genetics.109.107979
1943-2631
19786621
op_rights none
op_doi https://doi.org/10.1534/genetics.109.107979
container_title Genetics
container_volume 183
container_issue 4
container_start_page 1443
op_container_end_page 1452
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