PGC7, H3K9me2 and Tet3: regulators of DNA methylation in zygotes

Cell Res. 2013 Jan;23(1):6-9. doi: 10.1038/cr.2012.117. Epub 2012 Aug 7.

Abstract

In zygotes, a global loss of DNA methylation occurs selectively in the paternal pronucleus before the first cell division, concomitantly with the appearance of modified forms of 5-methylcytosine. The adjacent maternal pronucleus and certain paternally-imprinted loci are protected from this process. Nakamura et al. recently clarified the molecular mechanism involved: PGC7/Stella/Dppa3 binds to dimethylated histone 3 lysine 9 (H3K9me2), thereby blocking the activity of the Tet3 methylcytosine oxidase in the maternal genome as well as at certain imprinted loci in the paternal genome.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromosomal Proteins, Non-Histone
  • DNA Methylation*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Dioxygenases
  • Embryo, Mammalian / embryology
  • Embryo, Mammalian / metabolism
  • Embryonic Development
  • Female
  • Histones / genetics
  • Histones / metabolism*
  • Male
  • Mice
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism*
  • Zygote / cytology
  • Zygote / metabolism*

Substances

  • Chromosomal Proteins, Non-Histone
  • DNA-Binding Proteins
  • Dppa3 protein, mouse
  • Histones
  • Proto-Oncogene Proteins
  • Repressor Proteins
  • Dioxygenases
  • Tet3 protein, mouse