IGF2BP1 restricts the induction of human primordial germ cell fate in an m6A-dependent manner
- PMID: 40436019
- DOI: 10.1016/j.stem.2025.05.001
IGF2BP1 restricts the induction of human primordial germ cell fate in an m6A-dependent manner
Abstract
Primordial germ cells (PGCs) are specified early during embryogenesis and establish the germ cell lineage for transmitting genetic and epigenetic information from parents to offspring. However, whether N6-methyladenosine (m6A)-mediated epigenetic regulation is involved in the specification of PGCs remains elusive. In this study, we report that a knockout of m6A writers or overexpression of m6A erasers leads to an increased percentage of human PGC-like cells (hPGCLCs) induced from embryonic stem cells using a 3D aggregate system. We identify the m6A reader IGF2BP1 as the key factor for restricting hPGCLC fate induction by stabilizing OTX2 mRNAs in an m6A-dependent manner. In turn, OTX2 protein suppresses the function of TFAP2C via histone variant MacroH2A.1 during germ cell lineage specification. We also observe a similar role of Igf2bp1 in zebrafish in the induction of PGC fate. In summary, we identify an m6A-IGF2BP1-OTX2-MacroH2A.1-TFAP2C signaling axis that restricts the specification of human germ cell fate.
Keywords: IGF2BP1; MacroH2A.1; OTX2; PGC restrictors; TFAP2C; m(6)A modification; primordial germ cells.
Copyright © 2025 The Authors. Published by Elsevier Inc. All rights reserved.
Conflict of interest statement
Declaration of interests The authors declare no competing interests.