A plasmid-based lacZ gene assay for DNA polymerase fidelity

Abstract

A significantly improved DNA polymerase fidelity assay, based on a gapped plasmid containing the lacZα reporter gene in a single-stranded region, is described. Nicking at two sites flanking lacZα, and removing the excised strand by thermocycling in the presence of complementary competitor DNA, is used to generate the gap. Simple methods are presented for preparing the single-stranded competitor. The gapped plasmid can be purified, in high amounts and in a very pure state, using benzoylatednaphthoylated-DEAE-cellulose, resulting in a low background mutation frequency (~ 1x10). Two key parameters, the number of detectable sites and the expression frequency, necessary for measuring polymerase error rates have been determined. DNA polymerase fidelity is measured by gap filling, in vitro, followed by transformation into E. coli and scoring of blue/white colonies and converting the ratio to error rate. Several DNA polymerases have been used to fully validate this straightforward and highly sensitive system.

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Cite this paper

@inproceedings{Keith2017APL, title={A plasmid-based lacZ gene assay for DNA polymerase fidelity}, author={Brian J. Keith and Stanislaw K. Jozwiakowski and Bernard A. Connolly}, year={2017} }