Wu Kaiyue, Chen Qiran, Li Fang, Shen Jiadong, Sun Wei, Ge Chutian
College of Biological and Environmental Sciences, Zhejiang Wanli University, Ningbo, 315100, China.
MOE Key Laboratory of Marine Genetics and Breeding, College of Marine Life Sciences, Ocean University of China, Qingdao, 266003, China.
Cell Tissue Res. 2023 Oct;394(1):229-241. doi: 10.1007/s00441-023-03814-1. Epub 2023 Aug 1.
Meiotic entry is one of the earliest sex determination events of the germ cell in higher vertebrates. Although advances in meiosis onset have been achieved in mammals, birds and fish, how this process functions in reptiles is largely unknown. In this study, we present the molecular analysis of meiosis onset and the role of retinoic acid (RA) in this process in the red-eared slider turtle. Our results using Stra8 as a pre-meiosis indicator show that in the female embryonic gonad, meiosis commitment starts around stage 19. Additionally, signals of the meiosis marker Sycp3 could be detected at stage 19 and become highly expressed by stage 23. No expression of these genes was detected in male embryonic gonads, suggesting the entry into meiosis prophase I was restricted to female embryonic germ cells. Notably, RA activity in fetal gonads is likely to be elevated in females than that in males, as evidenced by the higher expression of RA synthase Aldh1a1 and lower expression of RA-degrading enzyme Cyp26a1 in female gonads prior to meiotic entry. In addition, exogenous RA treatment induced the expression of Stra8 and Sycp3 in both sexes, whether in vivo or in vitro. Together, these results indicate that high levels of RA in the embryonic female gonads can lead to the initiation of meiosis in the turtle.
减数分裂起始是高等脊椎动物生殖细胞中最早的性别决定事件之一。尽管在哺乳动物、鸟类和鱼类的减数分裂起始研究方面已取得进展,但该过程在爬行动物中如何发挥作用仍 largely 未知。在本研究中,我们展示了红耳龟减数分裂起始的分子分析以及视黄酸(RA)在此过程中的作用。我们使用 Stra8 作为减数分裂前指标的结果表明,在雌性胚胎性腺中,减数分裂承诺在第 19 阶段左右开始。此外,减数分裂标记物 Sycp3 的信号在第 19 阶段可被检测到,并在第 23 阶段高度表达。在雄性胚胎性腺中未检测到这些基因的表达,这表明进入减数分裂前期 I 仅限于雌性胚胎生殖细胞。值得注意的是,胎儿性腺中的 RA 活性在雌性中可能比在雄性中升高,这在减数分裂进入前雌性性腺中 RA 合成酶 Aldh1a1 的较高表达和 RA 降解酶 Cyp26a1 的较低表达中得到证明。此外,外源性 RA 处理在体内或体外均诱导了两性中 Stra8 和 Sycp3 的表达。总之,这些结果表明胚胎雌性性腺中高水平的 RA 可导致龟的减数分裂起始。