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

机译:基于NGS的方法来鉴定蛇头(Channa argus)中的性别特定标记

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摘要

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.
机译:我们描述了一种基于下一代测序(NGS)的方法,用于识别性别特异性标记,然后确定一个物种是否具有雄性或雌性异配子。为了测试该技术的准确性,我们检查了蛇头(Channa argus),这是中国经济上重要的淡水鱼。雄性的生长速度快于雌性,因此人们对开发将育种偏向全雄性以增加生物量产量的方法非常感兴趣。 NGS在雌性和雄性个体的DNA上进行,将雄性读段分裂为60 bp K-mers,并与由雌性读段组装的雌性参考基因组进行比对,未对齐的雄性K-mers-60保留在下一个过滤过程中。同时,收集了48位雌性的DNA样本并进行了测序,该数据进一步用于滤除先前未对齐的雄性K-mers-60。因此,筛选出候选Y染色体特异性序列的数目,通过PCR扩增在野生蛇头中验证了它们的性别特异性。最后,鉴定了三个Y染色体特异性片段(Contig-275834,Contig-359642和Contig-418354),并获得了特异性引物以区分蛇头的性别。此外,利用一对Contig-275834(275834X / Y-F和275834X / Y-R)引物来区分XX雌性,XY雄性和YY超级雄性,其不同长度的扩增产物针对不同性别而产生。因此,我们的工作证明了NGS数据在识别性别特异性标志物方面的能力,并且我们的研究中采用的方法可以应用于任何性别分化。此外,性别特异的标记物具有巨大的潜力,可以提高蛇头上所有雄性育种方法的效率。

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