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. 2025 Jul 3;32(7):1122-1138.e13.
doi: 10.1016/j.stem.2025.05.001. Epub 2025 May 27.

IGF2BP1 restricts the induction of human primordial germ cell fate in an m6A-dependent manner

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IGF2BP1 restricts the induction of human primordial germ cell fate in an m6A-dependent manner

Jin Zhang et al. Cell Stem Cell. .

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.

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Conflict of interest statement

Declaration of interests The authors declare no competing interests.