Previous Article | Next Article ![]()
J. Virol., Nov 1997, 8726-8734, Vol 71, No. 11
TR Serio, JL Kolman and G Miller
Late gene expression follows and is dependent upon lytic replication of the
viral genome. Although experimental evidence is lacking, lytic viral DNA
replication is believed to remove modifications or binding factors from the
genome which serve to repress late gene expression during latency or the
early lytic cycle. We have developed a reporter assay to begin
characterizing the mechanisms that regulate late gene expression in
Epstein-Barr virus (EBV). In this model system, the activities of late
promoter-reporter fusions are measured following transient transfection
into tissue culture cells expressing EBV during different stages of the
lytic cycle. This system faithfully recapitulates late expression patterns
from the endogenous virus, implicating specific cis-active sequences in the
control of late gene expression. In addition, these promoters respond only
indirectly to the viral immediate-early transactivator, ZEBRA. This
indirect response is mediated by other viral or virally induced activities
downstream of ZEBRA in the lytic cascade. In this system, late gene
expression is sensitive to inhibitors of the viral DNA polymerase such as
phosphonoacetic acid, although the reporters lack a eukaryotic origin of
replication and are not replicated under the assay conditions. Thus,
replication of the transcriptional template is not a prerequisite for
expression with late kinetics, a finding inconsistent with the current
models which posit a cis-active relationship between lytic EBV DNA
replication and late gene expression. Rather, analysis of this system has
revealed a trans relationship between late gene expression and viral DNA
replication and highlights the indirect and complex link between these two
events.
Copyright © 1997, American Society for Microbiology
Late gene expression from the Epstein-Barr virus BcLF1 and BFRF3 promoters does not require DNA replication in cis
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, Connecticut 06520, USA.
This article has been cited by other articles:
Copyright © 2009 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»