摘要
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.
| 原文 | 英語 |
|---|---|
| 頁(從 - 到) | 228-234 |
| 頁數 | 7 |
| 期刊 | Biochemical and Biophysical Research Communications |
| 卷 | 402 |
| 發行號 | 2 |
| DOIs | |
| 出版狀態 | 已出版 - 12 11 2010 |
指紋
深入研究「Targeted methylation of CMV and E1A viral promoters」主題。共同形成了獨特的指紋。引用此
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver