Read M L, Clark A R, Docherty K
Department of Medicine, University of Birmingham, Queen Elizabeth Hospital, U.K.
Biochem J. 1993 Oct 1;295 ( Pt 1)(Pt 1):233-7. doi: 10.1042/bj2950233.
Two important sequence elements, designated insulin enhancer binding site 1 (IEB1) or NIR and IEB2 or FAR, are involved in regulating expression of the rat insulin I gene. These elements bind a helix-loop-helix transcription factor, insulin enhancer factor 1 (IEF1). The IEB1 site is highly conserved among insulin genes but the IEB2 site is not conserved. To investigate the factors binding at the equivalent IEB1 and IEB2 sites in the human insulin gene enhancer, electrophoretic mobility shift assays were performed using a variety of cell extracts and probes specific for the homologous IEB1 and IEB2 sites. The results indicate that a factor with similar tissue distribution and binding characteristics to those of IEF1 binds to the IEB1 site in the human insulin gene, but that a separate factor, identified as the adenovirus major late transcription factor [MLTF, or upstream stimulating factor (USF)] binds to the IEB2 site.
两个重要的序列元件,即胰岛素增强子结合位点1(IEB1)或NIR以及IEB2或FAR,参与调控大鼠胰岛素I基因的表达。这些元件结合一种螺旋-环-螺旋转录因子,即胰岛素增强子因子1(IEF1)。IEB1位点在胰岛素基因中高度保守,但IEB2位点并不保守。为了研究在人胰岛素基因增强子中与等效的IEB1和IEB2位点结合的因子,使用多种细胞提取物和针对同源IEB1和IEB2位点的探针进行了电泳迁移率变动分析。结果表明,一种组织分布和结合特性与IEF1相似的因子与人胰岛素基因中的IEB1位点结合,但一种被鉴定为腺病毒主要晚期转录因子[MLTF,或上游刺激因子(USF)]的单独因子与IEB2位点结合。