Non-CpG methylation is prevalent in embryonic stem cells and may be mediated by DNA methyltransferase 3a

BH Ramsahoye, D Biniszkiewicz… - Proceedings of the …, 2000 - National Acad Sciences
BH Ramsahoye, D Biniszkiewicz, F Lyko, V Clark, AP Bird, R Jaenisch
Proceedings of the National Academy of Sciences, 2000National Acad Sciences
Current evidence indicates that methylation of cytosine in mammalian DNA is restricted to
both strands of the symmetrical sequence CpG, although there have been sporadic reports
that sequences other than CpG may also be methylated. We have used a dual-labeling
nearest neighbor technique and bisulphite genomic sequencing methods to investigate the
nearest neighbors of 5-methylcytosine residues in mammalian DNA. We find that embryonic
stem cells, but not somatic tissues, have significant cytosine-5 methylation at CpA and, to a …
Current evidence indicates that methylation of cytosine in mammalian DNA is restricted to both strands of the symmetrical sequence CpG, although there have been sporadic reports that sequences other than CpG may also be methylated. We have used a dual-labeling nearest neighbor technique and bisulphite genomic sequencing methods to investigate the nearest neighbors of 5-methylcytosine residues in mammalian DNA. We find that embryonic stem cells, but not somatic tissues, have significant cytosine-5 methylation at CpA and, to a lesser extent, at CpT. As the expression of the de novo methyltransferase Dnmt3a correlates well with the presence of non-CpG methylation, we asked whether Dnmt3a might be responsible for this modification. Analysis of genomic methylation in transgenic Drosophila expressing Dnmt3a reveals that Dnmt3a is predominantly a CpG methylase but also is able to induce methylation at CpA and at CpT.
National Acad Sciences