All transcripts of the human parvovirus B19 identified so far are regulated
by a single promoter at map unit 6 of the viral genome, the so-called p6 p
romoter. This promoter is active in a wide variety of different cells. In o
rder to identify cellular transcription factors involved in regulating prom
oter activity, we performed gel-retardation and supershift assays using the
parts of the p6 promoter sequence shown previously to be protected in foot
print experiments. Thereby, binding was demonstrated of the Oct-1 protein t
o an octamer motif within the p6 promoter and of the transcription factor S
p1 to three GC boxes. A specific preferential interaction of the factor Sp3
with one of these boxes was observed, indicating that the ratio Sp1:Sp3 ma
y be involved in the regulation of promoter activity, Consensus sites for t
he regulatory protein YY1 are located close to the GC boxes and the octamer
motif, to which this factor binds efficiently.