Table 3.
RPA/RFC/PCNA | Yeast |
Human | Mouse | |||||
---|---|---|---|---|---|---|---|---|
δexo+ |
δexo− |
η |
ηa | η | ||||
− | + | − | + | − | + | − | – | |
3′-CGATT | ||||||||
Sequencedb | 23 | 12 | 24 | 23 | 52c | 72 | 32 | 28 |
G → C | 1.4 | <0.7 | 8.5 | 4.8 | 17 | 12 | 34 | <23 |
G → T | 1.4 | 0.7 | 2.1 | 2.9 | <5.6 | 4.0 | 52 | 68 |
3′-CGoATT | ||||||||
Sequenced | 23 | 22 | 24 | 24 | 49 | 70 | 32 | 31 |
G → C | 1300 | <220 | 1000 | <160 | 41 | 76 | 300 | <20 |
G → T | 3100 | 4900 | 2900 | 3800 | 260 | 150 | 4400 | 4500 |
aAdditional experiments using a 45-mer template (see ‘Materials and Methods’ section) with slight sequence difference gave error rates of: (3′- … CGoATC …) G → C = 610 × 10−4, G → T = 4600 × 10−4; (3′- … CAGoTC …) G → C = <230 × 10−4, G → T = 4500 × 10−4; (3′- … CAGoT T …) G → C = 350 × 10−4 = 4000 × 10−4.
bDNA from dark blue plaques described in Table 2 was sequenced and error rates (×10−4) were calculated as previously described (42). Only changes at the G/8-oxoG site are given (the TAG stop codon is in italics in the left-most column). Note that G → A changes are not detectable by color screening as the amber stop codon (TAG) changes instead to an ochre stop codon (TAA) in the lacZα sequence.
cThese sequenced samples are the same as those used in a published report (50). The specific error rates shown here have not previously been reported.