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Publication Detail

Title: 5-azacytidine induces transgene silencing by DNA methylation in Chinese hamster cells.

Authors: Broday, L; Lee, Y W; Costa, M

Published In Mol Cell Biol, (1999 Apr)

Abstract: The cytosine analog 5-azacytidine (5-AzaC) is a demethylating agent that is also known to induce mutagenesis in mammalian cells. In this study, the mutagenic potential of this drug was tested in the G10 and G12 transgenic Chinese hamster cell lines, which have a single bacterial gpt gene integrated into the genome at different sites, with its expression driven by a simian virus 40 (SV40) promoter. We show that the mutation frequencies following a 48-h exposure to different concentrations of 5-AzaC were 10 to 20 times higher than those of any of the other numerous mutagens that have been tested in the G10-G12 system. Moreover, the mutation frequencies were much higher in the G10 cell line than in the G12 cells. Detailed molecular analysis of the 6-thioguanine (6-TG)-resistant variants demonstrated that transgene silencing by de novo DNA methylation and increased chromatin condensation in the SV40 promoter was the major factor responsible for this high level of 6-TG resistance. As would be expected, exposure to 5-AzaC lowered the overall genomic DNA methylation levels, but it unexpectedly caused hypermethylation and increased chromatin condensation of the transgene in both the G10 and G12 cell lines. These results provide the first evidence that 5-AzaC may also induce transgene-specific DNA methylation, a phenomenon that can further be used for the elucidation of the mechanism that controls silencing of foreign DNA.

PubMed ID: 10082586 Exiting the NIEHS site

MeSH Terms: Animals; Azacitidine/pharmacology*; Base Sequence; CHO Cells; Chromatin/ultrastructure; CpG Islands/genetics; Cricetinae; DNA Methylation*; Drug Resistance/genetics; Gene Expression Regulation; Hypoxanthine Phosphoribosyltransferase/genetics*; Molecular Sequence Data; Mutagenesis; Mutagens/pharmacology*; Thioguanine/pharmacology; Transgenes/drug effects*

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