Cleynen Isabelle, Brants Jan R, Peeters Kristel, Deckers Rob, Debiec-Rychter Maria, Sciot Raf, Van de Ven Wim J M, Petit Marleen M R
Department of Human Genetics, Flanders Interuniversity Institute for Biotechnology, University of Leuven, Herestraat 49, Box 602, B-3000 Leuven, Belgium.
Mol Cancer Res. 2007 Apr;5(4):363-72. doi: 10.1158/1541-7786.MCR-06-0331.
IMP2 (insulin-like growth factor-II mRNA binding protein 2) is an oncofetal protein that is aberrantly expressed in several types of cancer. We recently identified the Imp2 gene as a target gene of the architectural transcription factor HMGA2 (high mobility group A2) and its tumor-specific truncated form HMGA2Tr. In this study, we investigated the mechanism via which HMGA2 regulates Imp2 gene expression. We show that HMGA2 and HMGA2Tr directly regulate transcription of the Imp2 gene by binding to an AT-rich regulatory region located in the first intron. In reporter experiments, we show that this AT-rich regulatory region mimics the response of the endogenous Imp2 gene to HMGA2 and HMGA2Tr. Furthermore, we show that a consensus nuclear factor-kappaB (NF-kappaB) binding site located immediately adjacent to the AT-rich regulatory region binds NF-kappaB and that NF-kappaB and HMGA2 cooperate to regulate Imp2 gene expression. Finally, we provide evidence that there is a strong and statistically significant correlation between HMGA2 and IMP2 gene expression in human liposarcomas.
IMP2(胰岛素样生长因子-II mRNA结合蛋白2)是一种癌胚蛋白,在多种癌症中异常表达。我们最近将Imp2基因鉴定为结构转录因子HMGA2(高迁移率族蛋白A2)及其肿瘤特异性截短形式HMGA2Tr的靶基因。在本研究中,我们研究了HMGA2调节Imp2基因表达的机制。我们发现HMGA2和HMGA2Tr通过与位于第一个内含子中的富含AT的调控区域结合,直接调节Imp2基因的转录。在报告基因实验中,我们发现这个富含AT的调控区域模拟了内源性Imp2基因对HMGA2和HMGA2Tr的反应。此外,我们发现紧邻富含AT的调控区域的一个共有核因子-κB(NF-κB)结合位点可结合NF-κB,并且NF-κB与HMGA2协同调节Imp2基因表达。最后,我们提供证据表明,在人脂肪肉瘤中,HMGA2和IMP2基因表达之间存在强烈且具有统计学意义的相关性。