Regulation of expression of the Epstein-Barr virus BamHI-A rightward transcripts

被引:58
作者
Chen, HL
Huang, I
Wu, FY
Liao, GLL
Hutt-Fletcher, L
Hayward, SD
机构
[1] Johns Hopkins Univ, Sch Med, Sidney Kimmel Canc Ctr, Viral Oncol Program, Baltimore, MD 21231 USA
[2] Johns Hopkins Univ, Sch Med, Dept Pharmacol & Mol Sci, Baltimore, MD 21231 USA
[3] Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
[4] Louisiana State Univ, Hlth Sci Ctr, Dept Microbiol & Immunol, Shreveport, LA 71105 USA
关键词
D O I
10.1128/JVI.79.3.1724-1733.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The Epstein-Barr virus (EBV) BamHI-A rightward transcripts, or BARTs, are a family of mRNAs expressed in all EBV latency programs, including EBV-infected B cells in healthy carriers. Despite their ubiquitous expression, the regulation and biological function of BARTs are still unclear. In this study, the BART 5' termini were characterized by using a procedure that selects capped, full-length mRNAs. Two TATA-less promoter regions, designated P1 and P2, were mapped. PI had relatively high basal activity in both epithelial and B cells, whereas P2 exhibited higher activity in epithelial cells. Upon EBV infection of B cells, transcription from PI was detected soon after infection, while expression from P2 was delayed. Promoter-reporter assays in transiently transfected cells revealed that P1 and P2 were differentially regulated. Interferon regulatory factor 7 (IRF7) and IRF5 negatively regulated P1 activity. c-Myc and C/EBP family members positively regulated P2. Regulation of P2 by C/EBPs was characterized by electrophoretic mobility shift assay, chromatin immunoprecipitation, and reporter assays. More-abundant BART expression in epithelial cells correlated with the relative expression of positive and negative regulators in these cells.
引用
收藏
页码:1724 / 1733
页数:10
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