Lyttle C R, Damian-Matsumura P, Juul H, Butt T R
Department of Obstetrics and Gynecology, University of Pennsylvania, School of Medicine 19104-6140.
J Steroid Biochem Mol Biol. 1992 Aug;42(7):677-85. doi: 10.1016/0960-0760(92)90108-u.
An expression system that utilized yeast copper metallothionein promoter and ubiquitin fusion technology to express the human estrogen receptor gene in yeast is described. We have studied the biochemical and transcriptional regulatory properties of the human estrogen receptor. The biochemical properties of the yeast expressed receptors are identical to the receptors isolated from human tissue. Estradiol mediated activation of transcription by the receptor was studied by a reporter beta-galactosidase gene where expression was under the control of estrogen response elements. Using this expression system and a hyperpermeable yeast strain we have studied the effects of various antiestrogens on the regulation of estrogen receptor function. We demonstrate that tamoxifen and ICI 164,384 are capable of binding to the receptor but neither antiestrogen was able to block the estradiol mediated increase in transcription. In fact, both antiestrogens exerted weak agonist activity in this system.
描述了一种利用酵母铜金属硫蛋白启动子和泛素融合技术在酵母中表达人雌激素受体基因的表达系统。我们已经研究了人雌激素受体的生化和转录调控特性。酵母表达的受体的生化特性与从人体组织分离的受体相同。通过报告β-半乳糖苷酶基因研究了雌二醇介导的受体转录激活,该基因的表达受雌激素反应元件的控制。利用该表达系统和一种高渗透性酵母菌株,我们研究了各种抗雌激素对雌激素受体功能调节的影响。我们证明他莫昔芬和ICI 164,384能够与受体结合,但两种抗雌激素均不能阻断雌二醇介导的转录增加。事实上,两种抗雌激素在该系统中均表现出弱激动剂活性。