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Targeted methylation of CMV and E1A viral promoters

  • Chia Chen Hsu
  • , Hsin Pai Li
  • , Yu Hung Hung
  • , Yu Wei Leu
  • , Wu Hsiung Wu
  • , Feng Sheng Wang
  • , Kuan Der Lee
  • , Pey Jium Chang
  • , Chi Sheng Wu
  • , Yen Jung Lu
  • , Tim H.M. Huang
  • , Yu Sun Chang*
  • , Shu Huei Hsiao
  • *Corresponding author for this work
  • National Chung Cheng University
  • Chang Gung University
  • Ohio State University

Research output: Contribution to journal › Journal Article › peer-review

73 Scopus citations

Abstract

DNA methylation is a gene-silencing and host defense system that can down-regulate viral gene expression in mammalian cells. An established targeted DNA methylation method was used to demonstrate that genome-integrated CMV and adenovirus type 5 E1A promoters were hypermethylated after MCF7 and HEK293 cells were transfected with in vitro methylated viral promoter fragments. In both cases, the targeted methylation-induced gene silencing could be reversed by addition of 5-aza-2'-deoxycytidine, confirming that the CMV and E1A promoters are regulated by DNA methylation. The kinetics of the targeted DNA methylation was determined using a reporter system in live cells. In conclusion, targeted DNA methylation is able to efficiently silence susceptible viral promoters and provides an alternative strategy to study the impact of loci-specific DNA methylation in viral gene expression.

Original languageEnglish
Pages (from-to)228-234
Number of pages7
JournalBiochemical and Biophysical Research Communications
Volume402
Issue number2
DOIs
StatePublished - 12 11 2010

Keywords

  • DNA methylation
  • Epigenetics
  • Targeted DNA methylation
  • Two-component EGFP reporter system
  • Viral promoter

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