Abstract

BackgroundFish species often exhibit significant sexual dimorphism for commercially important traits. Accordingly, the control of phenotypic sex, and in particular the production of monosex cultures, is of particular interest to the aquaculture industry. Sex determination in the widely farmed Nile tilapia (Oreochromis niloticus) is complex, involving genomic regions on at least three chromosomes (chromosomes 1, 3 and 23) and interacting in certain cases with elevated early rearing temperature as well. Thus, sex ratios may vary substantially from 50%.ResultsThis study focused on mapping sex-determining quantitative trait loci (QTL) in families with skewed sex ratios. These included four families that showed an excess of males (male ratio varied between 64% and 93%) when reared at standard temperature (28°C) and a fifth family in which an excess of males (96%) was observed when fry were reared at 36°C for ten days from first feeding. All the samples used in the current study were genotyped for two single-nucleotide polymorphisms (rs397507167 and rs397507165) located in the expected major sex-determining region in linkage group 1 (LG 1). The only misassigned individuals were phenotypic males with the expected female genotype, suggesting that those offspring had undergone sex-reversal with respect to the major sex-determining locus. We mapped SNPs identified from double digest Restriction-site Associated DNA (ddRAD) sequencing in these five families. Three genetic maps were constructed consisting of 641, 175 and 1,155 SNPs from the three largest families. QTL analyses provided evidence for a novel genome-wide significant QTL in LG 20. Evidence was also found for another sex-determining QTL in the fifth family, in the proximal region of LG 1.ConclusionsOverall, the results from this study suggest that these previously undetected QTLs are involved in sex determination in the Nile tilapia, causing sex reversal (masculinisation) with respect to the XX genotype at the major sex-determining locus in LG 1.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1383-x) contains supplementary material, which is available to authorized users.

Highlights

  • Fish species often exhibit significant sexual dimorphism for commercially important traits

  • Since departures from equal sex ratio are not observed in all crosses, the usage of suitable crosses is a necessary prerequisite for mapping sex-determining quantitative trait loci (QTL) other than linkage group (LG) 1 in O. niloticus, and in particular previously undetected QTL

  • All the samples used in the current study were genotyped for two Single nucleotide polymorphism (SNP) markers located in the expected major sex-determining region in linkage group 1 (LG 1) and one microsatellite (UNH995) that is

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Summary

Introduction

Fish species often exhibit significant sexual dimorphism for commercially important traits. The sex chromosomes are still in early stages of differentiation compared to mammals, and do not show distinct differences in length or gene content [1] Instances of both XX/XY male heterogametic and WZ/ZZ female heterogametic sex-determining systems can be found in fish, while the fact that spontaneous sex-reversed XX males are generally fully fertile indicates that sex-determining regions can be located on autosomes. Many species of farmed fish exhibit sexual dimorphism in a range of traits of commercial importance, Palaiokostas et al BMC Genomics (2015) 16:171 including growth rate or age at maturity, stimulating research to clarify the sex determining system of such fish with the objective of the production of mono-sex stocks for the aquaculture industry. The major sex-determining region has been previously located on linkage group (LG) 1 [8] and fine mapped in a region of approximately 1.2 Mb [9]

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