Homeodomain transcription factor Hesx1/Rpx occupies Prop-1 activation sites in porcine follicle stimulating hormone (FSH) β subunit promoter
Homeodomain repressor factor Hesx1/Rpx plays a crucial role in the formation of Rathke’s pouch at the start of pituitary organogenesis and represses the Prop-1-dependent expression of Pit-1 gene, which promotes the differentiation of Pit-1-dependent hormone producing cells. Recently, we discovered a...
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Veröffentlicht in: | Biochemical and biophysical research communications 2007-06, Vol.357 (3), p.712-717 |
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Sprache: | eng |
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Zusammenfassung: | Homeodomain repressor factor Hesx1/Rpx plays a crucial role in the formation of Rathke’s pouch at the start of pituitary organogenesis and represses the Prop-1-dependent expression of Pit-1 gene, which promotes the differentiation of Pit-1-dependent hormone producing cells. Recently, we discovered a novel function of Prop-1 by which it activates the porcine follicle stimulating hormone β subunit (FSHβ) gene through Fd2 region (−852/−746). The present study aimed to determine whether Hesx1 exerts its role in the Prop-1-dependent activation of FSHβ gene.
Transient transfection assay for the porcine FSHβ promoter −985/+10, electrophoretic mobility shift assay (EMSA) and DNase I footprinting analysis for Fd2 region were carried out. Transfection assay in GH3 cells demonstrated that expression of Hesx1 alone does not change the promoter activity but the coexpression with Prop-1 represses the Prop-1-dependent activation of FSHβ promoter. Similar results were obtained for the mutant reporter vector deleting the region −745/−104 indicating that Fd2 region is a target site of Hesx1 as well as Prop-1. EMSA and DNase I footprinting analysis using recombinant Hesx1 and Prop-1 protein demonstrated that Hesx1 and Prop-1 certainly bind to the AT-rich regions in a different manner. These results suggest that Hesx1 blocks the advanced expression of FSHβ gene in the early stage of pituitary development, and Prop-1 thereafter appears and activates this gene. |
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ISSN: | 0006-291X 1090-2104 |
DOI: | 10.1016/j.bbrc.2007.03.197 |