Institute for the Advanced Study of Human Biology (ASHBi), Kyoto University, Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Department of Anatomy and Cell Biology, Graduate School of Medicine, Kyoto University, Yoshida-Konoe-cho, Sakyo-ku, Kyoto 606-8501, Japan.
Science. 2020 Mar 6;367(6482). doi: 10.1126/science.aaw4115. Epub 2020 Feb 13.
Sex determination of germ cells is vital to creating the sexual dichotomy of germ cell development, thereby ensuring sexual reproduction. However, the underlying mechanisms remain unclear. Here, we show that ZGLP1, a conserved transcriptional regulator with GATA-like zinc fingers, determines the oogenic fate in mice. ZGLP1 acts downstream of bone morphogenetic protein, but not retinoic acid (RA), and is essential for the oogenic program and meiotic entry. ZGLP1 overexpression induces differentiation of in vitro primordial germ cell-like cells (PGCLCs) into fetal oocytes by activating the oogenic programs repressed by Polycomb activities, whereas RA signaling contributes to oogenic program maturation and PGC program repression. Our findings elucidate the mechanism for mammalian oogenic fate determination, providing a foundation for promoting in vitro gametogenesis and reproductive medicine.
生殖细胞的性别决定对于形成生殖细胞发育的两性分化至关重要,从而确保有性繁殖。然而,其潜在机制尚不清楚。在这里,我们表明,具有 GATA 样锌指的保守转录调节剂 ZGLP1 决定了小鼠的卵母细胞命运。ZGLP1 作用于骨形态发生蛋白下游,但不是视黄酸(RA)下游,对于卵母细胞发生程序和减数分裂进入是必需的。ZGLP1 过表达通过激活由多梳抑制活性抑制的卵母细胞发生程序,诱导体外原始生殖细胞样细胞(PGCLCs)分化为胎儿卵母细胞,而 RA 信号转导有助于卵母细胞发生程序成熟和 PGC 程序抑制。我们的研究结果阐明了哺乳动物卵母细胞命运决定的机制,为促进体外配子发生和生殖医学提供了基础。