GFP-reporter for a high throughput assay to monitor estrogenic compounds

被引:21
作者
Beck, V [1 ]
Pfitscher, A [1 ]
Jungbauer, A [1 ]
机构
[1] Univ Nat Resources & Appl Life Sci, Dept Biotechnol, A-1190 Vienna, Austria
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2005年 / 64卷 / 01期
关键词
17; beta-estradiol; ethinylestradiol; mestranol; green fluorescent protein (GFP); reporter gene; estrogen receptor alpha;
D O I
10.1016/j.jbbm.2005.05.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
In vitro test systems using yeast cells are a useful tool for the determination of the estrogenic activity of estrogens, phyto- and xeno-estrogens and can be used for monitoring large sample numbers in a routine analysis procedure. Our conventional transactivation assay functions with an expression plasmid expressing estrogen receptor alpha (ER alpha) under the control of a copper-inducible CUP1 promoter and a reporter plasmid expressing beta-galactosidase under the control of the vitellogenin estrogen response element (ERE). In the novel yeast screen system the lacZ gene in the reporter plasmid was substituted by a gene for green fluorescent protein (GFP). Incubation of yeast with various concentrations of estrogenically active substances led to expression of the reporter gene product GFP in a dose dependent manner. The yeast transactivation assay was further down-scaled to be performed in a microplate scale, which is an important step to facilitate handling of large sample numbers. The sensitivity and reproducibility of the novel test system could be confirmed by analysis of the potencies of various estrogenically active substances. Thus, the newly developed yeast estrogen screen using GFP as a reporter can substitute the assay that has been used for a period of several years. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:19 / 37
页数:19
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