Methylation dynamics of IG-DMR and Gtl2-DMR during murine embryonic and placental development

Genomics. 2011 Aug;98(2):120-7. doi: 10.1016/j.ygeno.2011.05.003. Epub 2011 May 18.

Abstract

The Dlk1-Dio3 imprinted domain on mouse chromosome 12 contains IG-DMR and Gtl2-DMR, whose methylation patterns are established in the germline and after fertilization, respectively. In this study, we determine that acquisition of DNA methylation at the paternal allele of the Gtl2-DMR is initiated after the blastocyst stage and completed by embryonic day 6.5, and that Gtl2 (approved symbol: Meg3) is monoallelically expressed from the maternal allele as early as the blastocyst. Therefore, DNA methylation at the Gtl2-DMR is not a prerequisite for the imprinted expression of Gtl2, which may be involved in the control of proliferation and differentiation of cells during early gestation. We also reveal that a subregion of the IG-DMR exhibits tissue-specific differences in allelic methylation patterns. These results add to the growing body of knowledge elucidating the mechanism whereby parent-of-origin-dependent DNA methylation at the IG-DMR leads to the imprinted expression of the Dlk1-Dio3 cluster.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Animals
  • Calcium-Binding Proteins
  • Cell Differentiation / genetics
  • Cell Proliferation
  • DNA Methylation*
  • Epigenesis, Genetic
  • Female
  • Fetal Development / genetics*
  • Gene Expression Regulation, Developmental
  • Genomic Imprinting*
  • Germ Cells / metabolism
  • Intercellular Signaling Peptides and Proteins / genetics*
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Organ Specificity / genetics
  • Placentation / genetics*
  • Pregnancy
  • Proteins / genetics*
  • RNA, Long Noncoding
  • RNA, Untranslated / genetics

Substances

  • Calcium-Binding Proteins
  • Dlk1 protein, mouse
  • Intercellular Signaling Peptides and Proteins
  • MEG3 non-coding RNA, mouse
  • Proteins
  • RNA, Long Noncoding
  • RNA, Untranslated