| Literature DB >> 32054698 |
So I Nagaoka1,2, Fumio Nakaki2, Hidetaka Miyauchi2, Yoshiaki Nosaka1,2, Hiroshi Ohta1,2, Yukihiro Yabuta1,2, Kazuki Kurimoto2, Katsuhiko Hayashi2, Tomonori Nakamura1,2, Takuya Yamamoto1,3,4,5, Mitinori Saitou6,2,3.
Abstract
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.Entities:
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Year: 2020 PMID: 32054698 DOI: 10.1126/science.aaw4115
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728