Ayoubi T A, Jansen E, Meulemans S M, Van de Ven W J
Laboratory for Molecular Oncology, Center for Human Genetics, University of Leuven, Flanders Interuniversity Institute for Biotechnology, Herestraat 49, B-3000 Leuven, Belgium.
Oncogene. 1999 Sep 9;18(36):5076-87. doi: 10.1038/sj.onc.1202881.
The HMGIC gene has been implicated in the control of cell proliferation and development. We show here that HMGIC has multiple mRNA isoforms that arise by transcription initiation from alternative tandem promoters. These transcripts are not only differentially expressed between cell lines, but they can also differ within an individual cell line, in response to particular stimuli. Whereas quiescent 3T3-L1 preadipocytes express low levels of HMGIC mRNA, stimulation by serum results in a dramatic upregulation with the characteristics of a delayed-early response gene. Characterization of involved signal transduction pathways showed that both FGF-1 and PDGF-BB are strong inducers of HMGIC expression mediated via both the PI-3 kinase and MAP kinase pathways. In order to characterize the regulatory elements, sequences upstream of the translation initiation site of HMGIC were assayed for promoter activity. The HMGIC 5' flanking sequences had constitutive promoter activity in all cell lines tested, suggesting that HMGIC is regulated by negative regulatory elements that were not present in the 5'-flanking regions analysed here.
HMGIC基因与细胞增殖和发育的调控有关。我们在此表明,HMGIC有多种mRNA异构体,它们通过从交替串联启动子起始转录而产生。这些转录本不仅在细胞系之间差异表达,而且在单个细胞系内,响应特定刺激时也会有所不同。静止的3T3-L1前脂肪细胞表达低水平的HMGIC mRNA,血清刺激导致其显著上调,具有延迟早期反应基因的特征。对相关信号转导途径的表征表明,FGF-1和PDGF-BB都是通过PI-3激酶和MAP激酶途径介导的HMGIC表达的强诱导剂。为了表征调控元件,对HMGIC翻译起始位点上游的序列进行了启动子活性检测。HMGIC 5'侧翼序列在所有测试的细胞系中都具有组成型启动子活性,这表明HMGIC受此处分析的5'侧翼区域中不存在的负调控元件的调节。