Hamster flank organs are useful for studying androgen-dependent growth
of hair follicles and sebaceous glands. A cDNA clone (FAR-17a) was is
olated from the hamster flank organ, whose expression was highly sensi
tive to androgen. The mRNA level of this gene was reduced after castra
tion but reappeared after testosterone treatment. To elucidate the mec
hanism of expression of this gene regulated by androgen we isolated a
genomic clone, from a hamster genomic library, that includes the promo
ter and upsteam region. The promoter region was used to drive a lucife
rase reporter gene in Cos 7 cells. This construct was activated five t
o six times higher over a control plasmid lacking the promoter region.
We tested the effects of testosterone by transfection of the reporter
plasmid into androgen dependent SC-3 cells. The results showed up to
fivefold stimulation after the addition of androgen. The sequence of t
his promoter region was analyzed and the transcription factor binding
sites were predicted. Since no obvious androgen responsive elements we
re included in the promoter region, we suggest that the stimulation of
the reporter construct has to be mediated indirectly by androgen-depe
ndent transcription factor(s). (C) 1997 Elsevier Science Ireland Ltd.