Active DNA demethylation is required for complete imprint erasure in primordial germ cells

Sci Rep. 2014 Jan 13:4:3658. doi: 10.1038/srep03658.

Abstract

In mammalian primordial germ cells (PGCs), DNA demethylation is indispensible for parental imprint erasure, which is a reprogramming process essential for normal developmental potential. Thus, it is important to elucidate how DNA demethylation occurs in each imprinted region in PGCs and to determine which DNA demethylation pathway, passive or active, essentially contributes to the erasure of the imprint. Here, we report that active DNA demethylation via a putative Poly(ADP-ribose) polymerase (PARP) pathway is involved in H19-DMR imprint erasure in PGCs, as shown by an in vivo small molecule inhibitor assay. To the best of our knowledge, this is the first direct demonstration of a DNA replication-independent active DNA demethylation pathway in the erasure process of genomic imprinting in PGCs in vivo. The data also suggest that active DNA demethylation plays a significant role in the complete erasure of paternal imprinting in the female germ line.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • DNA Methylation* / drug effects
  • Embryo, Mammalian
  • Female
  • Gene Expression Regulation, Developmental
  • Genomic Imprinting*
  • Germ Cells / drug effects
  • Germ Cells / metabolism*
  • Male
  • Mice
  • Poly(ADP-ribose) Polymerase Inhibitors
  • Poly(ADP-ribose) Polymerases / metabolism
  • RNA, Long Noncoding / genetics

Substances

  • H19 long non-coding RNA
  • Poly(ADP-ribose) Polymerase Inhibitors
  • RNA, Long Noncoding
  • Poly(ADP-ribose) Polymerases