DNA Methyltransferase Is Actively Retained in the Cytoplasm during Early Development
Open Access
- 4 October 1999
- journal article
- Published by Rockefeller University Press in The Journal of cell biology
- Vol. 147 (1) , 25-32
- https://doi.org/10.1083/jcb.147.1.25
Abstract
The overall DNA methylation level sharply decreases from the zygote to the blastocyst stage despite the presence of high levels of DNA methyltransferase (Dnmt1). Surprisingly, the enzyme is localized in the cytoplasm of early embryos despite the presence of several functional nuclear localization signals. We mapped a region in the NH2-terminal, regulatory domain of Dnmt1 that is necessary and sufficient for cytoplasmic retention during early development. Altogether, our results suggest that Dnmt1 is actively retained in the cytoplasm, which prevents binding to its DNA substrate in the nucleus and thereby contributes to the erasure of gamete-specific epigenetic information during early mammalian development.Keywords
This publication has 44 references indexed in Scilit:
- New 5′ Regions of the Murine and Human Genes for DNA (Cytosine-5)-methyltransferaseJournal of Biological Chemistry, 1996
- DNA hypomethylation can activate Xist expression and silence X-linked genes.Genes & Development, 1996
- Role for DNA methylation in genomic imprintingNature, 1993
- Reversal of terminal differentiation and control of DNA replication: Cyclin A and cdk2 specifically localize at subnuclear sites of DNA replicationCell, 1993
- Targeted mutation of the DNA methyltransferase gene results in embryonic lethalityPublished by Elsevier ,1992
- Expression in mammalian cells of a cloned gene encoding murine DNA methyltransferaseGene, 1991
- Cloning and sequencing of a cDNA encoding DNA methyltransferase of mouse cellsJournal of Molecular Biology, 1988
- Karyophobic proteinsExperimental Cell Research, 1984
- Diffusive and nondiffusive proteins in vivo.The Journal of cell biology, 1984
- A reevaluation of the structure of purified tubulin in solution: evidence for the prevalence of oligomers over dimers at room temperature.The Journal of cell biology, 1984