PRDM14 extinction enables the initiation of trophoblast stem cell formation

Cell Mol Life Sci. 2024 May 6;81(1):208. doi: 10.1007/s00018-024-05237-9.

Abstract

Trophoblast stem cells (TSCs) can be chemically converted from embryonic stem cells (ESCs) in vitro. Although several transcription factors (TFs) have been recognized as essential for TSC formation, it remains unclear how differentiation cues link elimination of stemness with the establishment of TSC identity. Here, we show that PRDM14, a critical pluripotent circuitry component, is reduced during the formation of TSCs. The reduction is further shown to be due to the activation of Wnt/β-catenin signaling. The extinction of PRDM14 results in the erasure of H3K27me3 marks and chromatin opening in the gene loci of TSC TFs, including GATA3 and TFAP2C, which enables their expression and thus the initiation of the TSC formation process. Accordingly, PRDM14 reduction is proposed here as a critical event that couples elimination of stemness with the initiation of TSC formation. The present study provides novel insights into how induction signals initiate TSC formation.

Keywords: H3K27me3; Human trophoblast stem cells; PRDM14; Wnt.

MeSH terms

  • Animals
  • Cell Differentiation* / genetics
  • DNA-Binding Proteins* / genetics
  • DNA-Binding Proteins* / metabolism
  • GATA3 Transcription Factor / genetics
  • GATA3 Transcription Factor / metabolism
  • Histones / genetics
  • Histones / metabolism
  • Mice
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism
  • Stem Cells / cytology
  • Stem Cells / metabolism
  • Transcription Factor AP-2 / genetics
  • Transcription Factor AP-2 / metabolism
  • Transcription Factors* / genetics
  • Transcription Factors* / metabolism
  • Trophoblasts* / cytology
  • Trophoblasts* / metabolism
  • Wnt Signaling Pathway*

Substances

  • Transcription Factors
  • DNA-Binding Proteins
  • Prdm14 protein, mouse
  • GATA3 Transcription Factor
  • Transcription Factor AP-2
  • Tfap2c protein, mouse
  • RNA-Binding Proteins
  • Histones