Poly[d(G-m(5)C)] was modified by reductively activated mitomycin C, an
anti-tumour drug, under buffer conditions which are known to favour e
ither the B or the Z conformations of DNA. C.d. and P-31-n.m.r. were u
sed to characterize the poly[d(G-m(5)C)]-mitomycin cross-linked comple
xes, as well as the effects on the equilibrium between the B and Z for
ms of the polynucleotide. Mitomycin C appears to inhibit the B --> Z t
ransition, even in the presence of 3 mM MgCl2, while the Z-form of pol
y[d(G-m(5)C)] does not interact significantly with the drug under bifu
nctionally activating conditions; thus no reversion from the Z-form to
the B-form of the polynucleotide can be observed under the salt condi
tions which are required for the Z-form to exist.