ZGLP1 is a determinant for the oogenic fate in mice (ChIP-seq)

Mammalian sexual reproduction relies on the dichotomy of male and female germ cell development. 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 (BMP), 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 the 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. Overall design: 8 V5-ChIP-seq samples in 2 cell types with 2 treatments: c7 PGCLCs (Dox Only)_ChIP, c8 PGCLCs (Dox Only)_ChIP, c8 PGCLCs (Dox Only)_Input, c7 PGCLCs (Dox and RA), c8 PGCLCs (Dox and RA), c8 PGCLCs (Dox and RA)_Input, ESCs (Dox and RA)_ChIP, ESCs (Dox and RA)_Input