Structure of the human 5-HT 7 receptor gene and characterization of its promoter region

Abstract

The molecular mechanism regulating serotonin 5-HT 7 receptor expression is still unclear. In this study we provide evidence that transcription of the 5-HT 7 gene is at least partly regulated by Sp1 and Sp3. We isolated and sequenced > 3000 bp of the upstream sequences and identified by RACE a number of transcriptional initiation sites over a region of 300 bp upstream of the coding region. This region has a high GC content, but contains no obvious TATA or a CAAT box. Besides a Sp1/Sp3 consensus motif, regulatory elements for AP2, Egr-1 and MAZ are also present. Transient transfection assays using deletion variants indicated that the GC-rich region is essential for full promoter activity. The role of Sp1 in this was confirmed by transient overexpression of both wild type Sp1 or dominant-negative forms. By gel shift and supershift analyses, targeting the Sp1 consensus sequence and the GC-rich region just upstream of the transcription initiation sites, binding of Sp1 and Sp3 was demonstrated. Both in vitro as well as in vivo experiments, using a cell line which endogenously expresses the 5-HT 7 receptor, indicated that mithramycin A, an inhibitor of Sp1/3 transcription factor binding, was able to inhibit 5-HT 7 promoter activity. Taken together these results support the essential role of Sp factors in regulating 5-HT 7 promoter activity.