van Dijck P, Schoonjans K, Sassone-Corsi P, Auwerx J, Verhoeven G
Department of Developmental Biology, Campus Gasthuisberg, Leuven, Belgium.
Mol Cell Biochem. 1993 Aug 25;125(2):127-36. doi: 10.1007/BF00936441.
The hepatic expression of the alpha-2u-globulin gene family is controlled by a variety of hormones including steroids, growth hormone and insulin. The mechanisms by which these hormones affect alpha 2u-globulin expression are only partially understood. Recently we isolated and characterized clone RAP 01, an alpha 2u-globulin gene expressed in the liver. In preliminary experiments we noted that partial hepatectomy, a procedure which results in a sharp rise in the level of the oncoproteins c-Fos and c-Jun, also causes a transient induction of the messenger RNA corresponding to clone RAP 01. Using the DNAseI footprinting technique we were able to show that this clone contains a TPA (phorbol 12-myristate 13-acetate)-responsive element (TRE) in its first intron. This element (denoted as element X) is identical to the consensus AP-1 binding site (TGACTCAG) and is protected by rat liver nuclear extracts as well as by purified c-Jun. Gel retardation experiments show that an oligonucleotide containing the TRE consensus sequence competes for binding of liver nuclear proteins to element X and that antibodies directed against the M2 peptide of the mouse Fos protein or the PEP-2 peptide of Jun prevent the formation of specific complexes with the same element. Moreover, element X functions as a TRE in transfected BWTG3 hepatoma cells treated with TPA. Co-transfection with fos and jun expression vectors mimics the effects of TPA suggesting that AP-1 is in fact the mediator of the observed response. It is concluded that the first intron of RAP 01 contains a functional Fos-Jun element.
α-2u-球蛋白基因家族的肝脏表达受多种激素调控,包括类固醇、生长激素和胰岛素。这些激素影响α-2u-球蛋白表达的机制仅得到部分理解。最近,我们分离并鉴定了克隆RAP 01,这是一个在肝脏中表达的α-2u-球蛋白基因。在初步实验中,我们注意到部分肝切除术会导致癌蛋白c-Fos和c-Jun水平急剧上升,该手术还会引起与克隆RAP 01相对应的信使RNA的短暂诱导。使用DNA酶I足迹技术,我们能够证明该克隆在其第一个内含子中含有一个佛波酯12-肉豆蔻酸酯13-乙酸酯(TPA)反应元件(TRE)。这个元件(表示为元件X)与共有AP-1结合位点(TGACTCAG)相同,并受到大鼠肝核提取物以及纯化的c-Jun的保护。凝胶阻滞实验表明,含有TRE共有序列的寡核苷酸会竞争肝核蛋白与元件X的结合,并且针对小鼠Fos蛋白的M2肽或Jun的PEP-2肽的抗体可阻止与同一元件形成特异性复合物。此外,元件X在经TPA处理的转染BWTG3肝癌细胞中作为TRE发挥作用。与fos和jun表达载体共转染可模拟TPA的作用,这表明AP-1实际上是观察到的反应的介导者。得出的结论是,RAP 01的第一个内含子包含一个功能性的Fos-Jun元件。