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J. Virol., 06 1996, 3902-3908, Vol 70, No. 6
F He, WS Blair, J Fukushima and BR Cullen
The Bel-1 transcriptional transactivator encoded by human foamy virus (HFV)
can efficiently activate gene expression directed by both the HFV long
terminal repeat (LTR) and internal (Int) promoter elements. By DNA
footprinting and gel retardation analysis, we demonstrate that Bel-1 can
specifically bind to discrete sites in both the LTR and Int promoter
elements in vitro. However, transactivation of the HFV LTR by Bel-1 was
observed to require not only the promoter-proximal Bel-1 binding site
identified in vitro but also additional promoter-distal sequences. These
data suggest that Bel-1 binding is necessary but not sufficient for
efficient transactivation of Bel-1-responsive promoters in mammalian cells
and therefore raise the possibility that Bel-1 function may require the
action of a cellular DNA binding protein(s). Importantly, these data
demonstrate that Bel-1 is unique among retroviral regulatory proteins in
being a sequence-specific DNA binding protein.
Copyright © 1996, American Society for Microbiology
The human foamy virus Bel-1 transcription factor is a sequence-specific DNA binding protein
Department of Microbiology, Duke Medical Center, Durham North Carolina 27710, USA.
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