Hsu Hsiang-Yi, Chuang Chia-Hsien, Lu I-Hsuan, Lin Chung-Yen, Han Yu-San
Institute of Fisheries Science, College of Life Science, National Taiwan University, 1, Sec. 4, Roosevelt Rd., Taipei 10617, Taiwan. E-mail:
Institute of Information Science, Academia Sinica, Taipei 115, Taiwan. E-mail:
Zool Stud. 2023 Mar 10;62:e2. doi: 10.6620/ZS.2023.62-02. eCollection 2023.
The Japanese eel () is an important species in East Asian aquaculture. However, the production of seedlings for this purpose still depends on natural resources, as the commercial production of glass eels is not yet possible. Confusion about the sex of silver eels is one of the factors affecting the success rate of artificial maturation. This study sought to devise a harmless method to precisely assess the sex of silver eels. Partial pectoral fins were collected from females and males and the total RNA was extracted for transcriptomic analysis to identify sexually dimorphic genes as molecular markers for sex typing. An online database was constructed to integrate the annotations of transcripts and perform comparative transcriptome analysis. This analysis identified a total of 29 candidate sexually dimorphic genes. Ten were selected for a real-time quantitative polymerase chain reaction (RT-qPCR) to validate the transcriptomic data and evaluate their feasibility as markers. The transcriptomic analysis and RT-qPCR data implicated three potential markers (, , and ) in sex typing. The expression of was higher in females than in males. In contrast, the expression of and was higher in males than in females. The ΔC values of three markers were analyzed to determine their inferred thresholds, which can be used to determine the sex of Japanese eels. The results suggested that if a silver eel had a pectoral fin with the pectoral fin having the ΔC of < 11.3, the ΔC of > 11.4, or the ΔC of > 6.5 can be assessed it could be assessed as female. Males could be assessed by the ΔC of > 11.3, the ΔC of < 11.4, or the ΔC of < 6.5 in their pectoral fins. The molecular functions of these markers and the biological significance of their differential expression require further exploration.
日本鳗鲡()是东亚水产养殖中的重要物种。然而,由于目前尚无法实现玻璃鳗的商业化生产,用于此目的的鱼苗生产仍依赖自然资源。银鳗性别鉴定的混乱是影响人工成熟成功率的因素之一。本研究旨在设计一种无害方法来精确鉴定银鳗的性别。从雌性和雄性银鳗身上采集部分胸鳍,提取总RNA进行转录组分析,以鉴定性别二态性基因作为性别分型的分子标记。构建了一个在线数据库来整合转录本注释并进行比较转录组分析。该分析共鉴定出29个候选性别二态性基因。选择其中10个进行实时定量聚合酶链反应(RT-qPCR),以验证转录组数据并评估其作为标记的可行性。转录组分析和RT-qPCR数据表明有三个潜在标记(、和)可用于性别分型。在雌性中的表达高于雄性。相反,和在雄性中的表达高于雌性。分析了这三个标记的ΔC值以确定其推断阈值,可用于确定日本鳗鲡的性别。结果表明,如果一条银鳗胸鳍的ΔC<11.3、ΔC>11.4或ΔC>6.5,则可判定为雌性。雄性银鳗胸鳍的ΔC>11.3、ΔC<11.4或ΔC<6.5时可判定为雄性。这些标记的分子功能及其差异表达的生物学意义有待进一步探索。