GADD45 promotes locus-specific DNA demethylation and 2C cycling in embryonic stem cells

Genes Dev. 2019 Jul 1;33(13-14):782-798. doi: 10.1101/gad.325696.119. Epub 2019 Jun 6.

Abstract

Mouse embryonic stem cell (ESC) cultures contain a rare cell population of "2C-like" cells resembling two-cell embryos, the key stage of zygotic genome activation (ZGA). Little is known about positive regulators of the 2C-like state and two-cell stage embryos. Here we show that GADD45 (growth arrest and DNA damage 45) proteins, regulators of TET (TET methylcytosine dioxygenase)-mediated DNA demethylation, promote both states. Methylome analysis of Gadd45a,b,g triple-knockout (TKO) ESCs reveal locus-specific DNA hypermethylation of ∼7000 sites, which are enriched for enhancers and loci undergoing TET-TDG (thymine DNA glycosylase)-mediated demethylation. Gene expression is misregulated in TKOs, notably upon differentiation, and displays signatures of DNMT (DNA methyltransferase) and TET targets. TKOs manifest impaired transition into the 2C-like state and exhibit DNA hypermethylation and down-regulation of 2C-like state-specific genes. Gadd45a,b double-mutant mouse embryos display embryonic sublethality, deregulated ZGA gene expression, and developmental arrest. Our study reveals an unexpected role of GADD45 proteins in embryonic two-cell stage regulation.

Keywords: 5-hydroxymethylcytosine; GADD45; TET; ZGA; ZSCAN4; demethylation; two-cell embryo.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antigens, Differentiation / genetics*
  • Antigens, Differentiation / metabolism*
  • Cell Cycle Proteins / genetics*
  • Cell Cycle Proteins / metabolism*
  • Cells, Cultured
  • DNA Demethylation*
  • Embryonic Stem Cells / cytology*
  • Gene Expression Regulation, Developmental*
  • Gene Knockout Techniques
  • Mice
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism*

Substances

  • Antigens, Differentiation
  • Cell Cycle Proteins
  • Gadd45a protein, mouse
  • Gadd45b protein, mouse
  • Nuclear Proteins