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Journal of Virology, November 2000, p. 9845-9857, Vol. 74, No. 21
Department of Microbiology, College of
Medicine, University of Iowa, Iowa City, Iowa 52242
Received 17 April 2000/Accepted 28 July 2000
The human cytomegalovirus (HCMV) early UL4 promoter has served as a
useful model for studying the activation of early viral gene
expression. Previous transient-transfection experiments detected cis-acting elements (the NF-Y site and site 2) upstream of
the transcriptional start site (L. Huang and M. F. Stinski,
J. Virol. 69:7612-7621, 1995). The roles of two of these sites,
the NF-Y site and site 2, in the context of the viral genome were
investigated further by comparing mRNA levels from the early UL4
promoter in human foreskin fibroblasts infected by recombinant
viruses with either wild-type or mutant cis-acting
elements. Steady-state mRNA levels from the UL4 promoter with a
mutation in the NF-Y site were comparable to that of wild type. A
mutation in an Elk-1 site plus putative IE86 protein binding sites
decreased the steady-state mRNA levels compared to the wild type at
early times after infection. Electrophoretic mobility shift assays and
antibody supershifts detected the binding of cellular transcription
factor Elk-1 to site 2 DNA with infected nuclear extracts but not with
mock-infected nuclear extracts. The role of cellular transcription
factors activated by the mitogen activated protein kinase/extracellular
signal-regulated kinase pathway in activating transcription from early
viral promoters is discussed.
0022-538X/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Activation of Transcription of the Human Cytomegalovirus Early
UL4 Promoter by the Ets Transcription Factor Binding
Element
*
Corresponding author. Mailing address: Department of
Microbiology, College of Medicine, University of Iowa, Iowa City, Iowa 52242. Phone: (319) 335-7792. Fax: (319) 335-9006. E-mail:
mark-stinski{at}uiowa.edu.
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