Background. Hepatitis B virus (HBV)DNAhas been shown to containCpGislands that are methylated in human tissue, which suggests a role for methylation in regulating viral protein production. However, data are lacking about whether methylation regulates viral gene expression. Methods. To investigate the hypothesis that methylation of viral DNA regulates viral gene expression, unmethylated, partially methylated, and fully methylated viralDNAwas transfected into HepG2 cells. In addition, a new assay was designed that specifically identifies methylated covalently closed circular DNA (cccDNA) in human liver tissue. Results. Transfection of methylated HBV DNA led to reduced HBV mRNA levels in HepG2 cells, decreased surface and core protein expression in these cells, and decreased secretion of HBV viral proteins into the cell supernatant. These data provide direct evidence that CpG islands regulate gene transcription of HBV. Furthermore, methylated cccDNA was found in tumor and nonneoplastic human liver tissues. Finally, an in vitro equivalent of cccDNA showed decreased viral protein production in HepG2 cells after DNA methylation. Conclusion. Taken together, these data demonstrate that methylation of viral CpG islands can regulate viral protein production. © 2009 by the Infectious Diseases Society of America.
CITATION STYLE
Vivekanandan, P., Thomas, D., & Torbenson, M. (2009). Methylation regulates hepatitis b viral protein expression. Journal of Infectious Diseases, 199(9), 1286–1291. https://doi.org/10.1086/597614
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