Gu Ruoyi, Xu Jun, Lin Yixiang, Zhang Jing, Wang Huijun, Sheng Wei, Ma Duan, Ma Xiaojing, Huang Guoying
Children's Hospital of Fudan University, Shanghai, China.
Present address: Department of Pediatrics, Chengdu Women and Children's Medical Center, Sichuan, China.
Pediatr Res. 2016 Jul;80(1):159-68. doi: 10.1038/pr.2016.47. Epub 2016 Mar 18.
Retinoic acid X receptor alpha (RXRα) and Connexin 43 (Cx43) both play a crucial role in cardiogenesis. However, little is known about the interplay mechanism between the RXRα and Cx43.
The activations of retinoic acid response element (RARE) in Cx43 were measured by luciferase transfection assay. Electrophoretic mobility shift assay (EMSA) and chromatin immunoprecipitation (ChIP) was performed to prove that RXRα can directly bind to the RARE sequence. Quantitative real-time polymerase chain reaction (qRT-PCR) and western blotting were used to analyze the RXRα and Cx43 mRNA level and protein level in cells.
In this study, we confirmed the negative association of the gene expression between the RXRα and Cx43 in the cell level. Interestingly, a functional RARE was detected in the region from -1,426 to -314 base pairs upstream from the transcriptional start site of Cx43. Moreover, we also prove that RXRα can directly bind to this RARE sequence in vitro and in vivo.
RXRα negatively regulates the transcription and expression by directly binding to the RARE in the promoter of Cx43. The RARE-like sequence harbored in the Cx43 promoter region may serve as a functional RARE in the retinoic acid (RA) signaling pathway.
维甲酸X受体α(RXRα)和连接蛋白43(Cx43)在心脏发生过程中均发挥关键作用。然而,关于RXRα与Cx43之间的相互作用机制却知之甚少。
通过荧光素酶转染实验检测Cx43中维甲酸反应元件(RARE)的激活情况。进行电泳迁移率变动分析(EMSA)和染色质免疫沉淀(ChIP)以证明RXRα可直接结合至RARE序列。采用定量实时聚合酶链反应(qRT-PCR)和蛋白质免疫印迹法分析细胞中RXRα和Cx43的mRNA水平及蛋白质水平。
在本研究中,我们在细胞水平证实了RXRα与Cx43基因表达之间呈负相关。有趣的是,在Cx43转录起始位点上游-1,426至-314碱基对区域检测到一个功能性RARE。此外,我们还证明RXRα在体外和体内均可直接结合至该RARE序列。
RXRα通过直接结合至Cx43启动子中的RARE来负向调节转录和表达。Cx43启动子区域中存在的类RARE序列可能作为维甲酸(RA)信号通路中的功能性RARE。