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J. Biol. Chem., Vol. 259, Issue 3, 1566-1569, 02, 1984
KB Frank, JF Chiou and YC Cheng
The triphosphate of 9-(1,3-dihydroxy-2-propoxymethyl)guanine (DHPG)
competitively inhibits incorporation of dGTP into DNA catalyzed by DNA
polymerases specified by both type 1 and type 2 herpes simplex virus. K1
values were estimated to be 33 nM for type 1 and 46 nM for type 2-
specified DNA polymerase. DHPG acted as an alternate substrate to dGTP for
the virus-specified DNA polymerase. Incorporation of DHPG into DNA resulted
in the slowing down of the rate of DNA synthesis. The position of DHPG
incorporation was analyzed, and it was found to enter both internal and
terminal linkages. DNA which contained DHPG at termini was found to
competitively inhibit utilization of activated DNA as primer. DNA
polymerase alpha and DNA polymerases from several phosphonoformic
acid-resistant herpes simplex virus type 1 strains were examined for
sensitivity to 9-(1,3-dihydroxy-2-propoxymethyl)guanine triphosphate. A
lack of correlation between the in vivo sensitivities of the virus mutants
and the K1 values of the DNA polymerases was noted.
Interaction of herpes simplex virus-induced DNA polymerase with 9-(1,3- dihydroxy-2-propoxymethyl)guanine triphosphate
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