Wang Chiung-Min, Wang Raymond X, Liu Runhua, Yang Wei-Hsiung
Department of Biomedical Sciences, Mercer University School of Medicine, Savannah, GA 31404, USA.
Department of Genetics and Comprehensive Cancer Center, University of Alabama at Birmingham, Birmingham, AL 35294, USA.
Int J Mol Sci. 2017 Jan 31;18(2):304. doi: 10.3390/ijms18020304.
Jun dimerization protein 2 (JDP2), a basic leucine zipper transcription factor, is involved in numerous biological and cellular processes such as cancer development and regulation, cell-cycle regulation, skeletal muscle and osteoclast differentiation, progesterone receptor signaling, and antibacterial immunity. Though JDP2 is widely expressed in mammalian tissues, its function in gonads and adrenals (such as regulation of steroidogenesis and adrenal development) is largely unknown. Herein, we find that JDP2 mRNA and proteins are expressed in mouse adrenal gland tissues. Moreover, overexpression of JDP2 in Y1 mouse adrenocortical cancer cells increases the level of melanocortin 2 receptor (MC2R) protein. Notably, Mc2r promoter activity is activated by JDP2 in a dose-dependent manner. Next, by mapping the Mc2r promoter, we show that cAMP response elements (between -1320 and -720-bp) are mainly required for Mc2r activation by JDP2 and demonstrate that -830-bp is the major JDP2 binding site by real-time chromatin immunoprecipitation (ChIP) analysis. Mutations of cAMP response elements on Mc2r promoter disrupts JDP2 effect. Furthermore, we demonstrate that removal of phosphorylation of JDP2 results in attenuated transcriptional activity of Mc2r. Finally, we show that JDP2 is a candidate for SUMOylation and SUMOylation affects JDP2-mediated Mc2r transcriptional activity. Taken together, JDP2 acts as a novel transcriptional activator of the mouse Mc2r gene, suggesting that JDP2 may have physiological functions as a novel player in MC2R-mediated steroidogenesis as well as cell signaling in adrenal glands.
Jun二聚化蛋白2(JDP2)是一种碱性亮氨酸拉链转录因子,参与多种生物学和细胞过程,如癌症发展与调控、细胞周期调控、骨骼肌和破骨细胞分化、孕激素受体信号传导以及抗菌免疫。尽管JDP2在哺乳动物组织中广泛表达,但其在性腺和肾上腺中的功能(如类固醇生成和肾上腺发育的调控)在很大程度上尚不清楚。在此,我们发现JDP2 mRNA和蛋白在小鼠肾上腺组织中表达。此外,在Y1小鼠肾上腺皮质癌细胞中过表达JDP2可增加促黑素细胞激素2受体(MC2R)蛋白的水平。值得注意的是,JDP2以剂量依赖的方式激活Mc2r启动子活性。接下来,通过绘制Mc2r启动子图谱,我们表明环磷酸腺苷反应元件(-1320至-720碱基对之间)是JDP2激活Mc2r所必需的主要元件,并通过实时染色质免疫沉淀(ChIP)分析证明-830碱基对是主要的JDP2结合位点。Mc2r启动子上的环磷酸腺苷反应元件突变会破坏JDP2的作用。此外,我们证明去除JDP2的磷酸化会导致Mc2r转录活性减弱。最后,我们表明JDP2是SUMO化的候选对象,SUMO化会影响JDP2介导的Mc2r转录活性。综上所述,JDP2作为小鼠Mc2r基因的新型转录激活因子发挥作用,表明JDP2可能作为MC2R介导的类固醇生成以及肾上腺细胞信号传导中的新参与者具有生理功能。