Table 2.
Dox, ng/ml | Response in arbitrary light units of rtTA alleles
|
|||||
---|---|---|---|---|---|---|
— | rtTA | S2 | 19/56R | M1 | M2 | |
0 | 0.67 ± 0.28 | 1.24 ± 0.41 | 0.62 ± 0.48 | 2.54 ± 2.05 | 1.02 ± 1.16 | 3.02 ± 1.26 |
5 | 0.52 ± 0.06 | 57.27 ± 6.66 | 1.26 ± 0.17 | 3.24 ± 2.72 | 1.24 ± 1.54 | 17.07 ± 5.58 |
50 | 0.64 ± 0.55 | 229.72 ± 35.34 | 26.52 ± 12.4 | 0.91 ± 0.32 | 30.94 ± 25.75 | 1,517.37 ± 169.94 |
500 | 0.94 ± 0.63 | 696.27 ± 70.3 | 1,726.75 ± 110.64 | 112.68 ± 6.98 | 2,428.19 ± 254.42 | 10,746.33 ± 1,272.97 |
Dox-dependent gene activation of various rtTAs was measured in HeLa X1/6 cells that were transiently transfected with plasmids containing the genes for the transactivators rtTA and rtTA-S2, -19/56R, -M1, and -M2, all of which were controlled by PCMV. For standardization of transfection efficiencies, each transfection mixture contained also a vector that constitutively produces β-galactosidase. Cells were grown in absence of or in presence of 5, 50, and 500 ng/ml Dox. Twenty-four hours post transfection, luciferase activity was measured from cell extracts and normalized to β-galactosidase activity. Values given are arbitrary light units.