Thyroid hormones regulate rat thyrotropinβ gene promoter activity expressed in GH3 cells

Abstract

Thyroid hormones suppress the synthesis of TSH in part by decreasing the rate of α and TSHβ gene transcription. Cis-acting DNA sequences present in the rat TSHβ subunit gene that are induced in transcriptional regulation by thyroid hormone have been identified by deletion-mutation and transient expression studies. Plasmid expression vectors were constructed including 2900, 900, 204, 77, 17 base pairs (bp) of 5´-flanking sequence and exon (5´-untrans-lated sequence, transcriptional start sites) fused to the coding region of the bacterial chloramphenicol acetyltransferase (CAT) gene. The transfected chi-maeric plasmids demonstrated expression (with TSHβ DNA sequences in the 5´- to -3´-but not 3´- to -5´-orientation) in both a clonal pituitary cell line, GH3, and primary pituitary cell cultures, both of which are responsive to thyroid hormones. T3 (10-11 m to 10-7 m) treatment of transfected cells produced a dose-dependent decrease in CAT expression with a maximal 70% decrease at 10-8 m. While a decrease in the basal level of expression was noted with progressive removal of both 5´-flanking and intronic sequences adjacent to exon 1, the fold-decrease in response to T3 was equivalent even in the 57 bp construct. In contrast, T3 had no effect on CAT expression directed by the promoter of the herpes simplex virus thymidine kinase gene. Thus, the rat TSHβ gene 5´-flanking region can direct heterologous gene expression in GH3 cells and contains sequences which have properties of a putative cis-active T3 responsive regulatory element(s). The cis-element(s) resides within a 57 bp DNA fragment which includes 17 bases of 5´-flanking sequence, exon 1, and 13 bases of the first intron. © 1989 by The Endocrine Society.