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Valproate induces replication-independent active DNA demethylation.

Author	Nancy Detich, Veronica Bovenzi, Moshe Szyf
Citation Information	The Journal of biological chemistry, 278:27586-92 (2003)
Keywords	Blotting, Southern, Blotting, Western, Cell Line, CpG Islands, DNA, DNA Methylation, DNA Replication, Dose-Response Relationship, Drug, Enzyme Inhibitors, Green Fluorescent Proteins, Histones, Humans, Luminescent Proteins, Physical Chromosome Mapping, Plasmids, Precipitin Tests, Protein Binding, Sulfites, Transfection, Valproic Acid
Applications	Chromatin Immunoprecipitation
Related Products	17-295
Pub Med ID	12748177

In this report, we demonstrate that valproic acid (VPA), a drug that has been used for decades in the treatment of epilepsy and as a mood stabilizer, triggers replication-independent active demethylation of DNA. Thus, this drug can potentially reverse DNA methylation patterns and erase stable methylation imprints on DNA in non-dividing cells. Recent discoveries support a role for VPA in the regulation of methylated genes; however, the mechanism has been unclear because it is difficult to dissociate active demethylation from the absence of DNA methylation during DNA synthesis. We therefore took advantage of an assay that measures active DNA demethylation independently from other DNA methylation and DNA replication activities in human embryonal kidney 293 cells. We show that VPA induces histone acetylation, DNA demethylation, and expression of an ectopically methylated CMV-GFP plasmid in a dose-dependent manner. In contrast, valpromide, an analogue of VPA that does not induce histone acetylation, does not induce demethylation or expression of CMV-GFP. Furthermore, we illustrate that methylated DNA-binding protein 2/DNA demethylase (MBD2/dMTase) participates in this reaction since antisense knockdown of MBD2/dMTase attenuates VPA-induced demethylation. Taken together, our data support a new mechanism of action for VPA as enhancing intracellular demethylase activity through its effects on histone acetylation and raises the possibility that DNA methylation is reversible independent of DNA replication by commonly prescribed drugs.