Emmerling Verena Vanessa, Fischer Simon, Kleemann Michael, Handrick René, Kochanek Stefan, Otte Kerstin
Department of Gene Therapy, Ulm University, Helmholtz Strasse 8/1, 89081 Ulm, Germany.
Institute of Applied Biotechnology, Biberach University of Applied Sciences, Hubertus-Liebrecht-Strasse 35, 88400 Biberach, Germany.
Int J Biochem Cell Biol. 2016 Nov;80:81-86. doi: 10.1016/j.biocel.2016.09.022. Epub 2016 Sep 28.
MicroRNAs (miRNAs) are small non-coding RNAs that constitute a fundamental part of post-transcriptional gene regulation in mammalian cells. We have recently identified the intronic miR-483, which functions as an important regulator of protein synthesis during mild hypothermia in human and rodent cells. Since only very little is known about transcriptional regulation of intronic miRNAs and their host genes, we thoroughly investigated the regulation of miR-483 expression and its host gene IGF2 in HeLa cells. We demonstrate that miR-483 is regulated and expressed independently of its host gene IGF2 during mild hypothermia. Strikingly, we also discovered that miR-483 enhances its own transcription by up-regulation of the transcription factor USF1, which activates a promoter element upstream of the MIR483 gene. However, since the USF1 mRNA lacks binding sites for miR-483-5p and -3p, USF1 expression is likely enhanced in an indirect manner. Our results suggest that miR-483 may self-regulate its own expression independently of its host gene IGF2 in human HeLa cells. This points towards a novel feed-forward mechanism, in which selected intronic miRNAs may activate their own expression by transcriptional activation of upstream regulators.
微小RNA(miRNA)是小型非编码RNA,构成哺乳动物细胞转录后基因调控的基本组成部分。我们最近鉴定出内含子miR-483,其在人和啮齿动物细胞轻度低温期间作为蛋白质合成的重要调节因子发挥作用。由于对内含子miRNA及其宿主基因的转录调控知之甚少,我们深入研究了HeLa细胞中miR-483表达及其宿主基因IGF2的调控。我们证明,在轻度低温期间,miR-483的调控和表达独立于其宿主基因IGF2。引人注目的是,我们还发现miR-483通过上调转录因子USF1来增强自身转录,USF1激活MIR483基因上游的启动子元件。然而,由于USF1 mRNA缺乏miR-483-5p和-3p的结合位点,USF1的表达可能以间接方式增强。我们的结果表明,miR-483可能在人HeLa细胞中独立于其宿主基因IGF2自我调节自身表达。这指向一种新的前馈机制,其中选定的内含子miRNA可能通过上游调节因子的转录激活来激活自身表达。