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. Author manuscript; available in PMC: 2010 Sep 1.
Published in final edited form as: Biochimie. 2009 Jun 18;91(9):1163–1172. doi: 10.1016/j.biochi.2009.06.007

Table 1.

Mutation rates in the LacZ gapped DNA forward mutation assay.

WT D402A L606M Exo−/Exo+ ratio



Number detecteda Error rateb (×10−5) Number detected Error rate (×10−5) Number detected Error rate (×10−5)
Total Plaques 43,615 18,004 12,216
Total Mutants 54 155 159
Mutant Frequency 1.2 × 10−3 8.6 × 10−3 13 × 10−3
Base Substitutions 26 ≤0.45 69 4.4 73 6.7 7.2
+1 Insertions 9 0.077 30 1.2 42 2.4 ≥9.8
−1 Deletions 13 0.11 51 2.0 45 2.6 16
Large Deletions 3 6.9 (MF)c 13 72 (MF) 7 57 (MF) 18
Other Mutationsd 2 2 1
a

The total mutants reported may be greater or less than the sum of the different types of mutations because of the infrequent failure of a sequencing reaction, or the occasional presence of more than one distinct mutation in an individual plaque. Mutations were considered to be distinct as long as they were separated from each other by 3 or more nucleotides.

b

Background mutation frequencies are 3.4 × 10−4 for base substitutions and 0.55 × 10−4 for single base insertions and deletions, corresponding to background error rated of 0.45 × 10−5 for base substitutions and 0.046 × 10−5 for single base insertions and deletions [21].

c

The number of scorable sites for large deletion errors is not defined; therefore this value is given as a mutant frequency (MF) rather than an error rate.

d

Other mutations Pol δ were: WT, 2 occurrences of TTT to CTCT at +137 to +139; D402A, deletion of TA at −34 to −33, insertion of AC at −56 to −55; L606M, deletion of AC at −56 to −55.