Bose Sudeep, Ganguly Surajit, Kumar Sachin, Boockfor Fredric R
Amity Institute of Biotechnology, Amity University, Gautam Buddha Nagar, Sector-125, Noida, UP, 201313, India.
Laboratory of Molecular Dynamics, Department of Regenerative Medicine and Cell Biology, Medical University of South Carolina, Charleston, SC, 29425, USA.
Neurochem Res. 2016 Jun;41(6):1390-400. doi: 10.1007/s11064-016-1843-y. Epub 2016 Feb 15.
Recent evidence reveals that prolactin gene expression (PRL-GE) in mammotropes occurs in pulses, but the molecular process(es) underlying this phenomenon remains unclear. Earlier, we have identified an E-box (E-box133) in the rat PRL promoter that binds several circadian elements and is critical for this dynamic process. Preliminary analysis revealed a Pit-1 binding site (P2) located immediately adjacent to this E-box133 raising the possibility that some type of functional relationship may exist between these two promoter regions. In this study, using serum shocked GH3 cell culture system to synchronize PRL-GE activity, we determined that Pit-1 gene expression occurred in pulses with time phases similar to that for PRL. Interestingly, EMSA analysis not only confirmed Pit-1 binding to the P2 site, but also revealed an interaction with factor(s) binding to the adjacent E-box133 promoter element. Additionally, down-regulation of Pit-1 by siRNA reduced PRL levels during pulse periods. Thus, using multiple evidences, our results demonstrate clearly that the Pit-1 P2 site is necessary for PRL-GE elaboration. Furthermore, the proximity of this critical Pit-1 binding site (P2) and the E-box133 element coupled with the evidences of a site-to-site protein interactions suggest that the process of PRL-GE pulse activity might involve more dynamic and intricate cross-talks between promoter elements that may span some, or all, of the proximal region of the PRL promoter in driving its pulsatile expression.
最近的证据表明,促乳素基因表达(PRL-GE)在促乳腺细胞中呈脉冲式发生,但这一现象背后的分子过程仍不清楚。早些时候,我们在大鼠PRL启动子中鉴定出一个E盒(E-box133),它与几个昼夜节律元件结合,对这一动态过程至关重要。初步分析显示,一个Pit-1结合位点(P2)紧邻这个E-box133,这增加了这两个启动子区域之间可能存在某种功能关系的可能性。在本研究中,我们使用血清休克GH3细胞培养系统来同步PRL-GE活性,确定Pit-1基因表达呈脉冲式发生,其时间相位与PRL相似。有趣的是,电泳迁移率变动分析(EMSA)不仅证实了Pit-1与P2位点的结合,还揭示了它与结合在相邻E-box133启动子元件上的因子之间的相互作用。此外,通过小干扰RNA(siRNA)下调Pit-1可降低脉冲期的PRL水平。因此,我们的结果通过多项证据清楚地表明,Pit-1的P2位点对于PRL-GE的形成是必需的。此外,这个关键的Pit-1结合位点(P2)与E-box133元件的接近,以及位点间蛋白质相互作用的证据表明,PRL-GE脉冲活性过程可能涉及启动子元件之间更动态和复杂的相互作用,这些相互作用可能跨越PRL启动子近端区域的一部分或全部,以驱动其脉冲式表达。