González-Duarte Ramiro José, Cázares-Ordoñez Verna, Díaz Lorenza, Ortíz Víctor, Larrea Fernando, Avila Euclides
Department of Reproductive Biology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Vasco de Quiroga # 15, Col. Sección XVI, 14080, Mexico, D.F., Mexico.
School of Medicine, Universidad Nacional Autónoma de México, Circuito Interior, Ciudad Universitaria, Av. Universidad # 3000, 04510, Mexico, D.F., Mexico.
Mol Cell Biochem. 2015 Dec;410(1-2):65-73. doi: 10.1007/s11010-015-2538-4. Epub 2015 Aug 28.
The DEAD box RNA helicase DDX5 is a multifunctional protein involved in the regulatory events of gene expression. Herein, we presented evidence indicating that DDX5 is transcriptionally upregulated by calcitriol, the hormonal form of vitamin D3. In silico analysis revealed the presence of two putative vitamin D response elements (VDREs) in the DDX5 promoter region. Using luciferase reporter assays, we demonstrated that the DDX5 promoter containing these putative VDREs significantly increased the luciferase activity in vitamin D receptor (VDR)-positive SiHa cells upon calcitriol treatment. Electrophoretic mobility shift assays showed the ability of VDR and retinoid X receptor to interact only with the most proximal VDRE, while chromatin immunoprecipitation analysis confirmed the occupancy of this VDRE by the VDR. Finally, we demonstrated that calcitriol significantly increased both DDX5 mRNA and protein in SiHa cells. In summary, this study shows that DDX5 gene is transcriptionally upregulated by calcitriol through a VDRE located in its proximal promoter. Given the importance of DDX5 as a master regulator of differentiation programs, our study suggests that the pro-differentiating properties of calcitriol may be related with the induction of DDX5.
DEAD盒RNA解旋酶DDX5是一种多功能蛋白,参与基因表达的调控过程。在此,我们提供证据表明,DDX5在转录水平上被维生素D3的激素形式骨化三醇上调。计算机分析显示,DDX5启动子区域存在两个假定的维生素D反应元件(VDRE)。利用荧光素酶报告基因检测,我们证明含有这些假定VDRE的DDX5启动子在骨化三醇处理后,能显著增加维生素D受体(VDR)阳性的SiHa细胞中的荧光素酶活性。电泳迁移率变动分析表明,VDR和视黄酸X受体仅能与最靠近近端的VDRE相互作用,而染色质免疫沉淀分析证实VDR占据了该VDRE。最后,我们证明骨化三醇能显著增加SiHa细胞中DDX5的mRNA和蛋白水平。总之,本研究表明,骨化三醇通过位于其近端启动子的VDRE在转录水平上上调DDX5基因。鉴于DDX5作为分化程序的主要调节因子的重要性,我们的研究表明骨化三醇的促分化特性可能与DDX5的诱导有关。