TABLE 1.
Activation by: | Amt of dominant-negative AP-2 (μg) | Promoter activity
|
|
---|---|---|---|
−670 Bcl-2a | −134 Bcl-2b | ||
RB | 0 | 100.0 ± 0.5 | |
1 | 20.8 ± 2.8 | ||
2 | 6.4 ± 3.6 | ||
Basal level | 0 | 100.0 ± 0.5 | |
1 | 99.5 ± 0.2 | ||
2 | 89.5 ± 6.3 |
One-half microgram of −670 Bcl-2 CAT was transfected into MDCK cells either with 2.5 μg of pUC DNA or with pSV-RB expression vector, as indicated, plus increasing amounts of dominant-negative AP-2 in which the N-terminal region has been deleted. The activity of the −670 Bcl-2 CAT reporter in the presence of the control vector without the AP-2 sequence was set at 100%.
The negative control −134 Bcl-2 CAT vector, which does not contain the AP-2 binding site, was used. Its basal level was determined in a cotransfection assay with increasing amounts of dominent-negative AP-2.