Oncotarget

Research Papers:

An NGS-based approach for the identification of sex-specific markers in snakehead (Channa argus)

Mi Ou _, Cheng Yang, Qing Luo, Rong Huang, Ai-Di Zhang, Lan-Jie Liao, Yong-Ming Li, Li-Bo He, Zuo-Yan Zhu, Kun-Ci Chen and Ya-Ping Wang

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Oncotarget. 2017; 8:98733-98744. https://doi.org/10.18632/oncotarget.21924

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Abstract

Mi Ou1,2, Cheng Yang1,2, Qing Luo3, Rong Huang1, Ai-Di Zhang1, Lan-Jie Liao1, Yong-Ming Li1, Li-Bo He1, Zuo-Yan Zhu1, Kun-Ci Chen3 and Ya-Ping Wang1

1State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan 430072, China

2University of Chinese Academy of Sciences, Beijing 100049, China

3Pearl River Fisheries Research Institute, Chinese Academy of Fishery Sciences, Guangzhou 510380, China

Correspondence to:

Ya-Ping Wang, email: [email protected]

Kun-Ci Chen, email: [email protected]

Keywords: next generation sequencing; sex-specific molecular markers; snakehead

Received: April 19, 2017    Accepted: August 07, 2017    Published: October 19, 2017

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.


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