The adrenocorticotropin receptor or ACTH-R which is the type 2 among the me
lanocortin receptor family is almost exclusively expressed in the adrenal c
ortex, reflecting a high degree of tissue specificity. In human cultured ad
renocortical cells, we have previously reported that ACTH in contrast to mo
st of the peptide hormones, is able to up-regulate the number of its own re
ceptors through an increase of the transcriptional activity of the encoding
gene. Three putative SF-1 binding sites are present in the sequence of the
human ACTH-R gene promoter at -35 (SF-35), -98 (SF-98) and -209 (SF-209).
By EMSA studies, we demonstrated that these sites effectively bind SF-1 pro
tein. After transient transfection of H295R cells using a construct contain
ing the first 263 bp upstream of the transcriptional start site, in front o
f the luciferase gene in the pGL3 vector, we demonstrated the involvement o
f all three SF-1 sites to confer maximal constitutive activity to a proxima
l region of the hACTH-R gene promoter. Only SF-35 and SF-98 play a role in
cAMP-induced regulation of this gene.