Abstract

We described a next generation sequencing (NGS)-based approach to identify sex-specific markers and subsequently determine whether a species has male or female heterogamety. To test the accuracy of this technique, we examined the snakehead (Channa argus), which is economically important freshwater fish in China. Males grow faster than females, and there is significant interest in developing methods to skew breeding towards all-males to increase biomass yields. NGS was conducted on DNAs of individual female and male, the male reads were spitted into 60 bp K-mers and aligned to the female reference genome assembled by female reads, unaligned male K-mers-60 were kept in next filter process. Meanwhile, DNA sample of 48 females was pooled and sequenced, this data was further used to filter out the previous unaligned male K-mers-60. Hence, numbers of candidate Y chromosome-specific sequences were screened out, their sex-specificity were validated in wild snakeheads through PCR amplification. Finally, three Y chromosome-specific fragments (Contig-275834, Contig-359642, and Contig-418354) were identified, and specific primers were obtained to distinguish the sex of snakehead. Additionally, a pair of primers of Contig-275834 (275834X/Y-F and 275834X/Y-R) was exploited to distinguish XX females, XY males, and YY super-males, whose amplification products of different lengths were produced for different sexes. Therefore, our work demonstrated the ability of NGS data in identification of sex-specific markers, and the pipeline adopted in our study could be applied in any species of sex differentiation. Furthermore, the sex-specific markers have tremendous potential for improving the efficiency of all-male breeding practices in snakehead.

Highlights

  • The mechanisms of sex determination in animals are remarkably diverse

  • Three Y chromosome-specific fragments (Contig-275834, Contig-359642, and Contig-418354) were identified, and specific primers were obtained to distinguish the sex of snakehead

  • A pair of primers of Contig-275834 (275834X/Y-F and 275834X/Y-R) was exploited to distinguish XX females, XY males, and YY super-males, whose amplification products of different lengths were produced for different sexes

Read more

Summary

Introduction

The mechanisms of sex determination in animals are remarkably diverse As primitive vertebrates, it commonly has sex determination systems with either XX/XY (male heterogamety), or ZZ/ZW (female heterogamety) in fish [1]. Because some fish species display different growth rates and body sizes for different sexes, so all-female or all-male population production has significant economic implications in aquaculture [2, 3, 4]. Identifying the sex chromosome www.impactjournals.com/oncotarget system is typically done using one of three techniques: cytogenetic approaches that visualize heteromorphic sex chromosomes [5]; test cross experiments involving sexreversed fish [6]; or the identification of sex-specific molecular markers [7]. Hormonal sex reversal and test crosses are laborious and time consuming, the identification of sex-specific markers holds the most promise as an approach to identify sex chromosomes

Objectives
Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call