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Anatomy of the Varicella‐Zoster Virus Open‐Reading Frame 4 Promoter
Author(s) -
Eric J. Michael,
Karen M. Kuck,
Paul R. Kinchington
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/514273
Subject(s) - transactivation , open reading frame , biology , varicella zoster virus , transcription (linguistics) , transcriptional regulation , gene , promoter , transcription factor , genetics , regulation of gene expression , virus , virology , gene expression , microbiology and biotechnology , peptide sequence , linguistics , philosophy
The regulation of varicella-zoster virus (VZV) gene expression is largely controlled at the transcriptional level by a few key viral proteins cooperating with one another and with cellular transcription factors. However, the mechanisms involved are largely unclear. To identify the sequences important for the transcriptional regulation of open-reading frame (ORF) 4, itself encoding a transcriptional regulator, a mutation analysis of the promoter was done. These studies identified an element between -69 and -59 (relative to the transcriptional start site), which was critical to the activity of the promoter upon stimulation by the VZV transactivator IE62 and by VZV infection. DNA-protein interaction studies revealed that VZV induced the binding of a specific protein complex to this element, which contained the ubiquitous transcription factor USF. ORF 4 is the second VZV gene (in addition to VZV ORF 29) in which USF binding plays a critical role in gene expression.

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