Slater E P, Redeuilh G, Beato M
Institut für Molekularbiologie und Tumorforschung Philipps Universität, Marburg, Germany.
Mol Endocrinol. 1991 Mar;5(3):386-96. doi: 10.1210/mend-5-3-386.
Expression of the vitellogenin genes in avian and amphibian liver is regulated by estrogens. The DNA elements mediating estrogen induction of the various vitellogenin genes of chicken and Xenopus encompass one or more copies of a 13-mer palindromic sequence called the estrogen-responsive element (ERE). Here we show that upon incubation with the purified estrogen receptor (ER) from calf uterus the Xenopus vitellogenin A2 gene yields a DNase-I footprint over the ERE between -331 and -319. This element does not mediate the response to glucocorticoids or progestins in T47D cells. The three guanine residues in each half of the palindrome are protected against methylation by dimethylsulfate after incubation with ER, but not with glucocorticoid (GR) or progesterone (PR) receptors. In contrast, the chicken vitellogenin II gene exhibits multihormonal regulation by estrogens, progestins, and glucocorticoids in T47D and MCF7 cells. Regulation is mediated by the DNA region between -721 and -591 that contains four binding sites for hormone receptors, as demonstrated by DNase-I footprints and methylation protection experiments. The two distal and most proximal binding sites are recognized by ER, GR, and PR, whereas the central binding site is only bound by ER and GR. At suboptimal concentrations, estrogens and progestins or glucocorticoids act synergistically. In experiments using a DNA fragment containing an ERE adjacent to a glucocorticoid-responsive element/progesterone-responsive element, ER and PR bind synergistically to their corresponding sites, perhaps explaining the functional synergism of both hormones. Thus, two very different regulatory elements are used to mediate estrogen induction of related genes in chickens and amphibians.
雌激素可调控鸟类和两栖动物肝脏中卵黄蛋白原基因的表达。介导鸡和非洲爪蟾各种卵黄蛋白原基因雌激素诱导作用的DNA元件包含一个或多个被称为雌激素反应元件(ERE)的13聚体回文序列拷贝。在此我们表明,用从小牛子宫纯化的雌激素受体(ER)孵育后,非洲爪蟾卵黄蛋白原A2基因在-331至-319之间的ERE上产生一个DNA酶I足迹。该元件在T47D细胞中不介导对糖皮质激素或孕激素的反应。与ER孵育后,回文结构每一半中的三个鸟嘌呤残基可免受硫酸二甲酯甲基化作用的影响,但与糖皮质激素(GR)或孕激素(PR)受体孵育则不然。相比之下,鸡卵黄蛋白原II基因在T47D和MCF7细胞中表现出雌激素、孕激素和糖皮质激素的多激素调控。如DNA酶I足迹和甲基化保护实验所示,调控由-721至-591之间的DNA区域介导,该区域包含四个激素受体结合位点。两个远端及最近端的结合位点可被ER、GR和PR识别,而中间的结合位点仅被ER和GR结合。在次优浓度下,雌激素与孕激素或糖皮质激素协同作用。在使用含有与糖皮质激素反应元件/孕激素反应元件相邻的ERE的DNA片段进行的实验中,ER和PR协同结合至其相应位点,这或许解释了两种激素的功能协同作用。因此,鸡和两栖动物中用于介导相关基因雌激素诱导作用的是两个截然不同的调控元件。