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.
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
Chemicals
Apolipoprotein A-I
Oligodeoxyribonucleotides
DNA
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Shemer R
Department of Cellular Biochemistry, Hebrew University Medical School, Jerusalem, Israel.
Kafri T
O'Connell A
Eisenberg S
Breslow J L
Razin A
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