Induction of MRE-β-gal reporter by arsenic. BHK3038 were
treated with metals for 5 h. Total cell lysate was measured forβ-gal
activity as described under “Experimental Procedures.”
A–C, concentration curves of β-gal induction by
As3+, Cd2+, or Zn2+, respectively.
D, BHK3038 cells were transfected with pcDNA3.1HA.his (vector
control) or pMTF11–320 (dominant negative MTF1) for 48 h and
were treated with As3+ (1, 2, 5, and 10 μm),
Cd2+ (10 μm), tBHQ (30 μm), or
Zn2+ (100 μm) for 5 h. β-gal activity was
measured.