Novaira H J, Sonko M L, Radovick S
Department of Pediatrics, Division of Endocrinology, Johns Hopkins University School of Medicine, 600 North Wolfe St, Baltimore, MD, 21287, USA.
Mol Neurobiol. 2016 Jul;53(5):3315-3325. doi: 10.1007/s12035-015-9269-0. Epub 2015 Jun 17.
In vitro studies have demonstrated an increase in GnRH gene expression associated with an elevated secretory response to kisspeptin administration, suggesting that kisspeptin mediates GnRH expression at both the secretory and pretranslational levels. However, the kisspeptin-mediated intracellular mechanisms associated with the dynamic chromatin modifications modulating GnRH gene expression are unclear. The studies in this manuscript describe specific histone modifications on the enhancer and promoter of the mouse GnRH (mGnRH) gene induced by kisspeptin in GnRH neuronal cell lines (GT1-7 cells). ChIP assays followed by quantitative real-time PCR (qPCR) demonstrate that 15 and 45 min of 10(-9) M kisspeptin significantly increased histone 3 acetylation (H3Ac) at the kisspeptin response element (KsRE) contained between -3446 and -2806 bp of the mGnRH enhancer (GnRHen) in GT1-7 cells, while no changes were observed in the downstream neuron-specific element (NSE). Moreover, kisspeptin specifically induced acetylation of H3AcK14 and K27 and trimethylation of H3 lysine 4 at the KsRE (markers of active chromatin) and no changes in dimethylation of H3K9 (a marker associated with gene repression). Occupancy of RNA Pol II (RNAPII) and a differential carboxyl-terminal domain (CTD) phosphorylation pattern was observed. An interaction between the NSE and the KsRE via a chromatin loop in the mGnRH gene by kisspeptin was detected by the chromosome conformation capture assay (3C). In conclusion, these results demonstrate that kisspeptin induces histone acetylation/methylation and consequently enhances the formation of a chromatin loop in the mGnRH gene which results in known increase in kisspeptin-dependent mGnRH expression.
体外研究表明,给予 kisspeptin 后促性腺激素释放激素(GnRH)基因表达增加,且分泌反应增强,这表明 kisspeptin 在分泌水平和翻译前水平介导 GnRH 表达。然而,与调节 GnRH 基因表达的动态染色质修饰相关的 kisspeptin 介导的细胞内机制尚不清楚。本手稿中的研究描述了 kisspeptin 在 GnRH 神经元细胞系(GT1-7 细胞)中诱导的小鼠 GnRH(mGnRH)基因增强子和启动子上的特定组蛋白修饰。染色质免疫沉淀(ChIP)分析结合定量实时 PCR(qPCR)表明,10⁻⁹ M kisspeptin 作用 15 分钟和 45 分钟后,GT1-7 细胞中 mGnRH 增强子(GnRHen)-3446 至-2806 bp 之间的 kisspeptin 反应元件(KsRE)处的组蛋白 3 乙酰化(H3Ac)显著增加,而下游神经元特异性元件(NSE)未观察到变化。此外,kisspeptin 特异性诱导 KsRE 处 H3AcK14 和 K27 的乙酰化以及 H3 赖氨酸 4 的三甲基化(活性染色质标记),而 H3K9 的二甲基化(与基因抑制相关的标记)无变化。观察到 RNA 聚合酶 II(RNAPII)的占据情况和不同的羧基末端结构域(CTD)磷酸化模式。通过染色体构象捕获分析(3C)检测到 kisspeptin 通过 mGnRH 基因中的染色质环使 NSE 和 KsRE 之间发生相互作用。总之,这些结果表明 kisspeptin 诱导组蛋白乙酰化/甲基化,从而增强 mGnRH 基因中染色质环的形成,导致已知的 kisspeptin 依赖性 mGnRH 表达增加。