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Expression profiles of sex-related genes in gonads of genetic male Takifugu rubripes after 17 β-estradiol immersion

机译:17β-雌二醇浸没在遗传雄性红aki鱼性腺中性相关基因的表达谱

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摘要

Estradiol treatment during early life stages of tiger puffer Takifugu rubripes induces feminization in genetic males. However, the ovaries in genetic males may revert to testes once estradiol treatment is halted. Therefore studies should investigate molecular mechanisms underlying ovary-to-testis recovery in genetic males after treatment. In the present study, tiger puffer were exposed to 10, and 100 μg/L 17β-estradiol (E2) from 15 to 100 days post-hatching (dph), then gonad phenotypes and expression profiles of six sex-related genes (cyp19a, foxl2, dmrt1, amh, sox9a, and sox9b) were characterized after the exposure. Results showed that both 10 and 100 μg/L E2 induced ovarian development in genetic males at 100 dph. However, all ovaries induced by 10 μg/L E2 first developed into intersexual gonads and subsequently reverted to testes after the exposure. As for treatment of 100 μg/L E2, while the rest of the ovaries maintained morphological stability, percentages of intersexual gonads reached 38%-57%, and none were reverted to testes. Increased mRNA levels of cyp19a, foxl2 and sox9b and decreased mRNA levels of dmrt1, amh, and sox9a were observed during the ovarian development in genetic males. While contrary gene expression profiles were detected during ovary-to-testis transformation. The mRNA levels of all the six genes were increased during the development of intersexual gonads. These results indicated that up-regulation of dmrt1, amh and sox9a is associated with initial ovary-to-intersexual transformation, and suppression of foxl2, cyp19a and sox9b is essential for complete ovary-to-testis recovery in genetic males. This research will help to trace the molecular processes underlying gonadal transformation in teleosts.
机译:老虎河豚(Takifugu rubripes)生命早期的雌二醇治疗可诱导遗传男性中的女性化。但是,一旦停止雌二醇治疗,遗传男性的卵巢可能恢复为睾丸。因此,研究应调查治疗后遗传男性的卵巢到睾丸恢复的分子机制。在本研究中,老虎河豚在孵化后(dph)到15至100天暴露于10和100μg/ L17β-雌二醇(E2),然后暴露于六个性相关基因(cyp19a,暴露后对foxl2,dmrt1,amh,sox9a和sox9b)进行了表征。结果表明,在100 dph时,10和100μg/ L E2均可诱导遗传雄性卵巢发育。但是,由10μg/ L E2诱导的所有卵巢首先发育为两性腺,然后在暴露后恢复为睾丸。至于100μg/ L E2的治疗,其余卵巢保持形态稳定,而两性腺的性腺百分比达到38%-57%,没有一个恢复为睾丸。在男性卵巢发育过程中观察到cyp19a,foxl2和sox9b的mRNA水平升高,而dmrt1,amh和sox9a的mRNA水平降低。而相反的基因表达谱在卵巢到睾丸的转化过程中被检测到。在性交性腺的发育过程中,所有六个基因的mRNA水平均升高。这些结果表明,dmrt1,amh和sox9a的上调与最初的卵巢向双性恋转化有关,而foxl2,cyp19a和sox9b的抑制对于遗传雄性的从卵巢到睾丸的完全恢复至关重要。这项研究将有助于追踪硬骨鱼性腺转化的分子过程。

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  • 来源
    《中国海洋湖沼学报(英文版)》 |2019年第3期|1113-1124|共12页
  • 作者单位

    Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China;

    Function Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology & Function Laboratory for Marine Biology and Biotechnology, Qingdao 266000, China;

    Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China;

    Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China;

    Function Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology & Function Laboratory for Marine Biology and Biotechnology, Qingdao 266000, China;

    Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China;

    Function Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology & Function Laboratory for Marine Biology and Biotechnology, Qingdao 266000, China;

    Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China;

    Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao 266071, China;

    Function Laboratory for Marine Fisheries Science and Food Production Processes, Qingdao National Laboratory for Marine Science and Technology & Function Laboratory for Marine Biology and Biotechnology, Qingdao 266000, China;

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