Paulweber B, Sandhofer F, Levy-Wilson B
First Department of Internal Medicine, Landeskrankenanstalten Salzburg, Austria.
Mol Cell Biol. 1993 Mar;13(3):1534-46. doi: 10.1128/mcb.13.3.1534-1546.1993.
Previously, we showed that when a DNA fragment extending from -3067 to -2734 of the human apolipoprotein B (apo-B) gene is inserted immediately upstream of an apo-B promoter segment (-139 to +121), transcription from this promoter is reduced by about 10-fold in cultured colon carcinoma cells (CaCo-2) but not in cultured hepatoma cells (HepG2). We postulated that this reducer operates by a mechanism involving active repression of a transcriptional activator that binds to the segment from -111 to -88 of the apo-B promoter (B. Paulweber and B. Levy-Wilson, J. Biol. Chem. 266:24161-24168 1991). In the current study, the reducer element has been localized to a 24-bp sequence from -2801 to -2778 of the apo-B gene that contains a binding site for the negative regulatory protein ARP-1. Furthermore, we have demonstrated that the transcription factor hepatocyte nuclear factor 3 alpha (HNF-3 alpha) binds to the sequence 5'-TGTTTGCTTTTC-3' from -95 to -106 of the apo-B promoter, to stimulate transcription. Transcriptional activation by HNF-3 is repressed when the reducer sequence is inserted immediately upstream of the HNF-3 binding site, suggesting a mechanism by which the reducer-bound protein blocks the activation promoted by HNF-3. Data from cotransfection experiments in which ARP-1 is overexpressed in the absence of its binding site suggest that ARP-1 interacts either directly or via a mediator protein with proteins recognizing the HNF-3 site and that this interaction is sufficient to repress transcriptional activation by HNF-3. Because transcriptional activation by Sp1 is not affected by the reducer, it is unlikely that the reducer interacts directly with basic components of the transcriptional machinery.
此前,我们发现,当将一段从人载脂蛋白B(apo-B)基因的-3067延伸至-2734的DNA片段插入apo-B启动子片段(-139至+121)的紧上游时,该启动子的转录在培养的结肠癌细胞(CaCo-2)中降低了约10倍,但在培养的肝癌细胞(HepG2)中却没有。我们推测,这种抑制因子通过一种机制发挥作用,该机制涉及对与apo-B启动子的-111至-88片段结合的转录激活因子的活性抑制(B. Paulweber和B. Levy-Wilson,《生物化学杂志》266:24161 - 24168,1991)。在当前研究中,抑制因子元件已定位到apo-B基因从-2801至-2778的一段24碱基对序列,该序列包含负调节蛋白ARP-1的一个结合位点。此外,我们已经证明,转录因子肝细胞核因子3α(HNF-3α)与apo-B启动子从-95至-106的5'-TGTTTGCTTTTC-3'序列结合,以刺激转录。当抑制因子序列插入HNF-3结合位点的紧上游时,HNF-3的转录激活受到抑制,这表明抑制因子结合蛋白阻断HNF-3促进的激活的一种机制。在不存在其结合位点的情况下过表达ARP-1的共转染实验数据表明,ARP-1直接或通过一种介导蛋白与识别HNF-3位点的蛋白相互作用,并且这种相互作用足以抑制HNF-3的转录激活。因为Sp1的转录激活不受抑制因子的影响,所以抑制因子不太可能直接与转录机制的基本成分相互作用。