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甲胎蛋白近端增强子:定位、细胞特异性及地塞米松的调节作用

The alpha-foetoprotein proximal enhancer: localization, cell specificity and modulation by dexamethasone.

作者信息

Houart C, Szpirer J, Szpirer C

机构信息

Département de Biologie Moléculaire, Université Libre de Bruxelles, Rhode-St-Genèse, Belgium.

出版信息

Nucleic Acids Res. 1990 Nov 11;18(21):6277-82. doi: 10.1093/nar/18.21.6277.

Abstract

The enhancer element present in the 5' proximal region flanking the mouse alpha-foetoprotein (AFP) gene, active in AFP-producing hepatoma cells and inactive in non-producing hepatoma cells, was localized between positions -203 and -79. This enhancer segment contains a sequence resembling the steroid hormone response element. We demonstrated that this sequence is dispensable for the enhancer activity but mediates dose-dependent effects of dexamethasone on the enhancer activity: dexamethasone decreases the proximal enhancer activity at low concentrations but this inhibitory effect vanishes at high concentrations. Our results indicate that several transcriptional factors, one of which is absent in AFP-non-producing hepatoma cells, control the AFP proximal enhancer activity.

摘要

小鼠甲胎蛋白(AFP)基因侧翼5'近端区域存在的增强子元件,在产生AFP的肝癌细胞中具有活性,而在不产生AFP的肝癌细胞中无活性,其定位在-203至-79位之间。该增强子片段包含一个类似于类固醇激素反应元件的序列。我们证明该序列对于增强子活性并非必需,但介导地塞米松对增强子活性的剂量依赖性效应:地塞米松在低浓度时降低近端增强子活性,但这种抑制作用在高浓度时消失。我们的结果表明,几种转录因子控制AFP近端增强子活性,其中一种在不产生AFP的肝癌细胞中不存在。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/69e9/332492/eab7ea219230/nar00205-0094-a.jpg

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