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J. Biol. Chem., Vol. 259, Issue 3, 1539-1545, 02, 1984
TA Kunkel, LA Loeb and MF Goodman
The fidelity with which wild type T4 DNA polymerase copies phi X174 amber 3
plus strand DNA at position 587 in vitro has been measured. Synthesis is
initiated by hybridizing to the template a HaeIII restriction fragment
whose 3'-OH terminus is 83 nucleotides from the amber 3 site. Based on gel
electrophoresis of product DNA molecules and genetic marker rescue data, T4
DNA polymerase copies significantly beyond the mutant site. Transfection
analysis shows that the A X T leads to G X C mutation at position 587
occurs 10- to 100-fold less frequently with T4 DNA polymerase than with E.
coli DNA polymerase I. The aberrant incorporation of cytosine opposite
adenine at position 587 by the T4 polymerase alone is occurring at a
frequency not greater than about 10(-7) which, for this particular locus,
may be similar to the fidelity exhibited by the T4 accessory proteins plus
the polymerase comprising the replication complex. A comparison of the
accuracy of mutator L56 and antimutator L141 T4 DNA polymerases relative to
wild type shows at most a 2- to 4-fold decrease and increase, respectively,
in fidelity. When compared to 10- to 1000-fold effects on mutation
frequencies that these same mutant alleles have in vivo, these results
suggest that the wide range in expression of mutator and antimutator
phenotypes in vivo may be dependent on an abnormal interaction of the
aberrant DNA polymerases with other protein components of the replication
complex.
On the fidelity of DNA replication. The accuracy of T4 DNA polymerases in copying phi X174 DNA in vitro
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