TABLE 1.
PROS AND CONS OF USING YEAST TO STUDY NUCLEAR RECEPTORS
| Yeast | Tissue Culture Cells |
|---|---|
| Ligand-dependent transactivation of nuclear receptors possible. Compounds that act as antagonists in tissue culture cells behave as partial agonists in yeast. | Cell and promoter selective agonist and antagonist function can be reconstructed. |
| Pure heterodimeric and multimeric interactions possible with nuclear receptors. | Not possible due to endogenous nuclear receptors. |
| Ligands are not metabolized. | Ligands are metabolized in mammalian cells. |
| Unique (simple) basal transcription context. | Physiological relevance of the unique context, depending upon the promoter and cell line. |
| Can produce large amounts of a receptor protein. | Incompatible with cell physiology. |
| Complementation cloning to discover novel orphans or partners (i.e., RIPs and TRIPs). | Not possible or very time consuming. |
| Stable transformants. HTS engine, parallel screens possible using robotics. | Transfection of DNA required. Data from stable cell lines may not be reliable. |