Neuroscience Section, Papé Family Pediatric Research Institute, Department of Pediatrics.
Mol Cell Biol. 2013 Jul;33(14):2650-8. doi: 10.1128/MCB.00094-13. Epub 2013 May 13.
The molecular basis underlying the physiologically well-defined orexigenic function of glucocorticoid (Gc) is unclear. Brain-specific homeobox factor (Bsx) is a positive regulator of the orexigenic neuropeptide, agouti-related peptide (AgRP), in AgRP neurons of the hypothalamic arcuate nucleus. Here, we show that in response to fasting-elevated Gc levels, Gc receptor (GR) and Bsx synergize to direct activation of AgRP transcription. This synergy is dictated by unique sequence features in a novel Gc response element in AgRP (AgRP-GRE). In contrast to AgRP-GRE, Bsx suppresses transactivation directed by many conventional GREs, functioning as a gene context-dependent modulator of GR actions or a target selector for GR. Consistent with this finding, AgRP-GRE drives fasting-dependent activation of a target gene specifically in GR(+) Bsx(+) AgRP neurons. These results define AgRP as a common orexigenic target gene of GR and Bsx and provide an opportunity to identify their additional common targets, facilitating our understanding of the molecular basis underlying the orexigenic activity of Gc and Bsx.
糖皮质激素(Gc)具有明确的生理食欲刺激功能,但其潜在的分子基础仍不清楚。脑特异性同源盒因子(Bsx)是下丘脑弓状核中食欲肽 AgRP 神经元中食欲肽 AgRP 的正调控因子。在这里,我们发现,在饥饿引起的 Gc 水平升高的情况下,Gc 受体(GR)和 Bsx 协同作用,直接激活 AgRP 的转录。这种协同作用是由 AgRP 中新型 Gc 反应元件(AgRP-GRE)中的独特序列特征决定的。与 AgRP-GRE 不同的是,Bsx 抑制了许多常规 GRE 指导的转录激活,作为 GR 作用的基因上下文依赖性调节剂或 GR 的靶标选择器。与这一发现一致的是,AgRP-GRE 驱动靶基因在 GR(+)Bsx(+)AgRP 神经元中的饥饿依赖性激活。这些结果将 AgRP 定义为 GR 和 Bsx 的共同食欲刺激靶基因,并为鉴定它们的其他共同靶基因提供了机会,有助于我们理解 Gc 和 Bsx 的食欲刺激活性的分子基础。