. 2003 Nov 5;100(24):14247–14252. doi: 10.1073/pnas.2332176100

Table 1. Percentages of frameshift mutations detected in progeny of dG-, PdG, and M₁G-adducted M13MB102–1 transformed into WT or repair-deficient E. coli strains.

	dG^*	M₁G-1	M₁G-2	M₁G-3	M₁G-4	dG	PdG-1	PdG-2	PdG-3	PdG-4
LM102^†	<0.03	0.10	0.2 ± 0.2	0.4 ± 0.3	0.2 ± 0.1	<0.05	<0.03	<0.03	<0.03	0.04 ± 0.03
LM103 (uvrA^–)	0.02	0.4 ± 0.3	0.4 ± 0.1	1.0 ± 0.3	0.5 ± 0.2	<0.03	0.5 ± 0.3	0.10 ± 0.01	0.20 ± 0.06	0.30 ± 0.07

Sequence designations are as follows: 5′-GGTGTCCG₁CG₂CG₃CG₄GCATG-3′, where G_n = dG, M₁G, or PdG

^†

Results are expressed as mutation frequencies ± SD × 10² and were obtained by screening 1,000 plaques per experiment for each probe. Values are the average of three independent constructions, transformations, and hybridizations

Table 1. Percentages of frameshift mutations detected in progeny of dG-, PdG, and M1G-adducted M13MB102–1 transformed into WT or repair-deficient E. coli strains.

Table 1. Percentages of frameshift mutations detected in progeny of dG-, PdG, and M₁G-adducted M13MB102–1 transformed into WT or repair-deficient E. coli strains.