Two waves of de novo methylation during mouse germ cell development. Academic Article uri icon

Overview

MeSH

  • Animals
  • Cellular Reprogramming
  • Epigenesis, Genetic
  • Male
  • Mice
  • RNA, Small Interfering
  • Transcription, Genetic

MeSH Major

  • DNA Methylation
  • Retroelements
  • Spermatocytes
  • Spermatogenesis

abstract

  • During development, mammalian germ cells reprogram their epigenomes via a genome-wide erasure and de novo rewriting of DNA methylation marks. We know little of how methylation patterns are specifically determined. The piRNA pathway is thought to target the bulk of retrotransposon methylation. Here we show that most retrotransposon sequences are modified by default de novo methylation. However, potentially active retrotransposon copies evade this initial wave, likely mimicking features of protein-coding genes. These elements remain transcriptionally active and become targets of piRNA-mediated methylation. Thus, we posit that these two waves play essential roles in resetting germ cell epigenomes at each generation. © 2014 Molaro et al.; Published by Cold Spring Harbor Laboratory Press.

publication date

  • July 15, 2014

has subject area

  • Animals
  • Cellular Reprogramming
  • DNA Methylation
  • Epigenesis, Genetic
  • Male
  • Mice
  • RNA, Small Interfering
  • Retroelements
  • Spermatocytes
  • Spermatogenesis
  • Transcription, Genetic

Research

keywords

  • Journal Article

Identity

Language

  • eng

PubMed Central ID

  • PMC4102761

Digital Object Identifier (DOI)

  • 10.1101/gad.244350.114

PubMed ID

  • 25030694

Additional Document Info

start page

  • 1544

end page

  • 1549

volume

  • 28

number

  • 14