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Updated: Aug 19, 2026

Reverse Yeast Two-hybrid System to Identify Mammalian Nuclear Receptor Residues that Interact with Ligands and/or Antagonists
Published on: November 15, 2013
The human mineralocorticoid receptor only partially differentiates between different ligands after expression in
Matthias Bureik1, Nicole Brück, Katja Hübel
1Department of Biochemistry, Saarland University, Postfach 151150. D-66041 Saarbrücken, Germany. mabu@mx.unisaarland.de
Abstract:
Cardiac failure is a major health problem with increasing incidence due to aging of the population. Studies in both experimental animals and humans have suggested that aldosterone excess may have deleterious effects on cardiac function. In order to generate a novel screening system for the identification of aldosterone antagonists, we expressed the human mineralocorticoid receptor (MR) and the human glucocorticoid receptor (GR), respectively, in the fission yeast Schizosaccharomyces pombe. Reporter plasmids containing two hormone-responsive elements upstream of a fission yeast minimal promotor and either a lacZ gene (for quantification) or a neomycin gene (for survival screening) were constructed and cotransformed into fission yeast strains with expression plasmids for MR or GR. The functionality of the reporter systems was then tested using physiological ligands of both receptors as well as known inhibitors. Transactivating activity of MR could be stimulated by aldosterone, 11-deoxycorticosterone, 11-deoxycortisol, cortisol, cortisone, and spironolactone, but not by progesterone, while GR activity was stimulated by cortisol and cortisone, but also not by progesterone. Taken together, we have succeeded in establishing fission yeast-based screening systems that allow the identification of MR- or GR-interacting compounds. Moreover, our data show that after expression in fission yeast both receptors did not differentiate between steroids with different configurations at positions 11beta, 17 and 18. This finding suggests that only recognition of C-21 substituents may be accomplished by the receptor proteins alone, while the physiologically important selectivity towards other positions of the steroid ligand depends on other factors which are not conserved from fission yeast to man.
Insights
Scientists developed a novel fission yeast screening system to identify aldosterone antagonists. This system aids in discovering new drugs for cardiac conditions linked to aldosterone excess.
Area of Science:
- Molecular Biology
- Pharmacology
- Yeast Genetics
Background:
- Cardiac failure is a growing health concern, with aldosterone excess implicated in detrimental cardiac effects.
- Existing methods for identifying aldosterone antagonists are limited, necessitating novel screening approaches.
Purpose of the Study:
- To establish a novel, high-throughput screening system in fission yeast for identifying mineralocorticoid receptor (MR) and glucocorticoid receptor (GR) antagonists.
- To investigate the ligand-binding specificity of human MR and GR expressed in fission yeast.
Main Methods:
- Human MR and GR were expressed in the fission yeast Schizosaccharomyces pombe.
- Reporter plasmids containing hormone-responsive elements linked to reporter genes (lacZ or neomycin) were constructed.
- Yeast strains were co-transformed with receptor and reporter plasmids, and functionality was tested with various steroid ligands and inhibitors.
Main Results:
- The fission yeast system successfully demonstrated transactivation activity for MR and GR in response to specific steroid ligands.
- MR activity was stimulated by aldosterone and related steroids, while GR activity was stimulated by cortisol and cortisone.
- Both receptors, when expressed in yeast, showed limited discrimination between steroids with differing configurations at positions 11beta, 17, and 18.
Conclusions:
- A functional fission yeast-based screening system for identifying MR and GR modulators has been successfully established.
- The study highlights that steroid selectivity beyond C-21 substituents may rely on factors not conserved between yeast and humans.
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