Yang Yang, Liu Qinghua, Xiao Yongshuang, Xu Shihong, Wang Xueying, Yang Jingkun, Song Zongcheng, You Feng, Li Jun
CAS Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, China; University of Chinese Academy of Sciences, Beijing 100049, China; Center for Ocean Mega-Science, Chinese Academy of Sciences, 7 Nanhai Road, Qingdao 266071, China.
CAS Key Laboratory of Experimental Marine Biology, Institute of Oceanology, Chinese Academy of Sciences, Qingdao 266071, China; Laboratory for Marine Biology and Biotechnology, Qingdao National Laboratory for Marine Science and Technology, Qingdao 266071, China; Center for Ocean Mega-Science, Chinese Academy of Sciences, 7 Nanhai Road, Qingdao 266071, China.
Gen Comp Endocrinol. 2019 Apr 1;274:17-25. doi: 10.1016/j.ygcen.2018.12.012. Epub 2018 Dec 27.
In teleosts, sex is plastic and is influenced by environmental factors. Elevated temperatures have masculinizing effects on the phenotypic sex of certain sensitive species. In this study, we reared genetic XX Japanese flounder at a high temperature (27.5 ± 0.5 °C) and obtained a population of sex-reversal XX males (male ratio, 95.24%). We comparatively analyzed the dynamic characteristics of germ cells and gsdf (gonadal soma-derived factor) expression during sexual differentiation for the experimental (27.5 ± 0.5 °C) and control (18 °C ± 0.5 °C) groups. The results revealed that the germ cell proliferation inhibited and gsdf expression up-regulated in the experimental group, and the gsdf mRNA and proteins expressed in somatic cells that had direct contact with germline stem cells (with Nanos 2 protein expression) including spermatogonia and oogonia by ISH (in situ hybridization) and IHC (immunohistochemistry). In addition, we also overexpressed the gsdf in XX flounders, and the germ cell number of XX flounders bearing gsdf gene significantly decreased and sometimes disappeared completely, which was consistent with the results from high-temperature induction. Therefore, based on all the results, we speculated that the high expression of gsdf might inhibit germ cell proliferation during sex differentiation, and eventually cause sex reversal in the high-temperature induced masculinization of XX Japanese flounder.
在硬骨鱼类中,性别具有可塑性且受环境因素影响。高温对某些敏感物种的表型性别具有雄性化作用。在本研究中,我们将遗传型XX的日本牙鲆在高温(27.5±0.5°C)下饲养,获得了一群性逆转的XX雄性个体(雄性比例为95.24%)。我们对实验组(27.5±0.5°C)和对照组(18°C±0.5°C)在性别分化过程中生殖细胞的动态特征以及gsdf(性腺体细胞衍生因子)的表达进行了比较分析。结果显示,实验组中生殖细胞增殖受到抑制,gsdf表达上调,并且通过原位杂交(ISH)和免疫组织化学(IHC)发现,gsdf mRNA和蛋白在与生殖系干细胞直接接触的体细胞(具有Nanos 2蛋白表达)中表达,包括精原细胞和卵原细胞。此外,我们还在XX牙鲆中过表达了gsdf,携带gsdf基因的XX牙鲆的生殖细胞数量显著减少,有时甚至完全消失,这与高温诱导的结果一致。因此,基于所有这些结果,我们推测gsdf的高表达可能在性别分化过程中抑制生殖细胞增殖,并最终导致XX日本牙鲆在高温诱导的雄性化过程中发生性逆转。