Methylation changes in the apolipoprotein AI gene during embryonic development of the mouse

Proc Natl Acad Sci U S A. 1991 Dec 15;88(24):11300-4. doi: 10.1073/pnas.88.24.11300.

Abstract

We report here a detailed study of developmental changes in the methylation status of specific sites in a single-copy tissue-specific gene, from the germ cell through the early embryo to adult tissues. Two sites at the 5' end of the mouse apolipoprotein AI gene were unmethylated in the ovulated unfertilized oocytes and methylated in the sperm. In contrast, a third site, located upstream of the gene, was methylated and a CpG island within the gene was unmethylated in both oocyte and sperm. The methylated sites, regardless of maternal or paternal origin, underwent demethylation in the early embryo (8-16 cells) and stayed unmethylated through the late blastocyst stage. During gastrulation, non-CpG island sites underwent methylation, followed by gradual demethylation at specific sites in tissues parallel to expression of the gene (liver and intestine). The formation of the mature tissue-specific methylation pattern of the apolipoprotein AI gene, therefore, involves the following three major events: (i) erasure of the germ-cell methylation pattern (at the 8- to 16-cell stage), (ii) formation of a new methylation pattern by de novo methylation of non-CpG island sites (during gastrulation), and (iii) tissue-specific demethylation associated with the onset of expression of the gene.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Aging
  • Animals
  • Apolipoprotein A-I / genetics*
  • Base Sequence
  • Crosses, Genetic
  • DNA / genetics*
  • Embryonic and Fetal Development*
  • Female
  • Humans
  • Male
  • Methylation
  • Mice
  • Mice, Inbred Strains
  • Mice, Transgenic
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides
  • Organ Specificity
  • Ovum / physiology
  • Polymerase Chain Reaction / methods
  • Restriction Mapping
  • Spermatozoa / physiology

Substances

  • Apolipoprotein A-I
  • Oligodeoxyribonucleotides
  • DNA