Host: The Japanese Society of Toxicology
Epigenetic toxicity is thought to be caused by the disruption of epigenetic regulation due to chemical exposure. We constructed a novel in vitro system for detection of alterations in DNA methylation status by chemicals. In Neuro-2a, we introduced a reporter system by selecting Agouti-IAP and Daz1 as promoters. Using 5azaC, we found an increase in luciferase activity, suggesting a decrease in methylation. Pyrosequencing confirmed the decrease in DNA methylation. Thus, we could develop a convenient cellular system for detection of modifying effect of chemicals on DNA methylation status.