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. 2006 Jan;188(2):733–744. doi: 10.1128/JB.188.2.733-744.2006

TABLE 4.

Expression of ICE-lacZ and Fur box-lacZ reporter fusions in S. cerevisiae strains synthesizing Gal4′-′Irr or Gal4′-′Fur hybrid prey proteinsa

Yeast strain Target β-Galactosidase activity (Miller units)
Gal4′-′Irr Gal4′-′Fur
8730 ICEhmu 36.1 ± 9.7 0.0
8732 ICEhmumut 0.0 ND
8733 ICE6680 10.1 ± 1.3 0.0
8734 ICE7895 93.5 ± 8.4 0.0
8765 Fur box ND 5.3 ± 0.3
a

Cells of yeast reporter strains were transfected with prey plasmid pRJ8737 (Gal4′-′Irr) or pRJ8735 (Gal4′-′Fur). Cultures grew in synthetic dropout medium (−URA, −LEU) for 3 to 5 h until they reached mid-exponential phase (optical density at 600 nm of 0.5 to 0.8), and one-hybrid interactions were examined as β-galactosidase activity. Activity was measured from two cultures per strain, each assayed in duplicate. Control yeast strains 8730, 8733, 8734 and 8765 harboring the vector pGAD424 (encoding Gal4′ only) showed no β-galactosidase activity. Data are shown for one out of four independent experiments, all yielding similar results. ND, not done.