Orphan Receptor Chicken Ovalbumin Upstream Promoter Transcription Factors Inhibit Steroid Factor-1, Upstream Stimulatory Factor, and Activator Protein-1 Activation of Ovine Follicle-Stimulating Hormone Receptor Expression via Composite cis-Elements
The FSH receptor (FSHR) is selectively expressed in the granulosa and Sertoli cells in a development-dependent manner. Little is known regarding how the regulatory factors balance expression of this gene in ovarian cycles or spermatogenic stages. We have used the ovine FSHR promoter as a model syste...
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Veröffentlicht in: | Biology of reproduction 2002-06, Vol.66 (6), p.1656-1666 |
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Sprache: | eng |
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Zusammenfassung: | The FSH receptor (FSHR) is selectively expressed in the granulosa and Sertoli cells in a development-dependent manner. Little
is known regarding how the regulatory factors balance expression of this gene in ovarian cycles or spermatogenic stages. We
have used the ovine FSHR promoter as a model system and identified a third regulatory element (RE-3) located at â197 to â171
of the strongest promoter. Gel mobility shift and antibody supershift assays demonstrated that nuclear factors c-Fos/c-Jun,
steroidogenic factor-1 (SF-1), upstream stimulatory factor-1/2 (USF-1/2), and chicken ovalbumin upstream promoter transcription
factor-1/2 (COUP-TFI/II) potentially bound to RE-3. We have also extended our previous observations by showing that a sequence
containing an E-box was not only bound by USF proteins but also recognized by COUP-TF orphan receptors. Functional studies
demonstrated that USF-1/2, c-Fos/c-Jun, and SF-1 were activators, whereas COUP-TFs were repressors. Our studies indicated
that RE-3 mediated SF-1 activation as well as phorbol 12-myristate 13-acetate stimulation, whereas COUP-TFs inhibited AP-1,
USFs, and SF-1 activation. We also demonstrated that both COUP-TF-binding sites in the core promoter were required for the
bipartite elements to oppose their competitor binding. These data suggest a mechanism by which positive and negative regulators
compete for the common regulatory elements, providing antagonistic pathways that might govern the expression of FSHR in gonadal
cells. |
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ISSN: | 0006-3363 1529-7268 |
DOI: | 10.1095/biolreprod66.6.1656 |