Department of Reproductive Medicine and the Center for Reproductive Science and Medicine, University of California San Diego, La Jolla, California 92093, USA.
Endocrinology. 2012 Apr;153(4):2023-33. doi: 10.1210/en.2011-1763. Epub 2012 Jan 31.
Differential regulation of gonadotropin hormone production in the pituitary is critical for fertility. Activin and progesterone signaling in gonadotrope cells is important for Fshb gene expression. Previously, we reported that synergy between activin and progestins required the binding of SMAD proteins and the progesterone receptor (PR) to the murine Fshb promoter. In this study, we demonstrate that the FOXL2 transcription factor is also necessary for the full synergistic response between activin and progestins. We show that this synergy occurs in a species-specific manner and that multiple elements in the Fshb promoter that bind forkhead box L2 (FOXL2), SMA/mothers against decapentaplegic homologs (SMAD), and PR are required. Furthermore, we demonstrate that FOXL2 can physically interact with PR and SMAD3. Thus, it is likely that protein-protein interactions among FOXL2, SMAD, and PR recruited to the Fshb promoter play a key role in facilitating Fshb transcription before the secondary FSH surge in rodents.
垂体中促性腺激素分泌的差异调节对于生育能力至关重要。激活素和孕激素在促性腺激素细胞中的信号传导对于 Fshb 基因的表达很重要。先前,我们报道了激活素和孕激素之间的协同作用需要 SMAD 蛋白和孕激素受体 (PR) 与小鼠 Fshb 启动子结合。在这项研究中,我们证明了 FOXL2 转录因子对于激活素和孕激素之间的完全协同反应也是必需的。我们表明,这种协同作用以种属特异性的方式发生,并且 Fshb 启动子中结合叉头框 L2 (FOXL2)、 SMA/抗 decapentaplegic 同源物 (SMAD) 和 PR 的多个元件是必需的。此外,我们证明 FOXL2 可以与 PR 和 SMAD3 进行物理相互作用。因此,FOXL2、SMAD 和 PR 招募到 Fshb 启动子上的蛋白-蛋白相互作用可能在啮齿动物中第二次 FSH 激增之前促进 Fshb 转录中起关键作用。