Table 1. Base substitution specificity of allelic variant W438 of human Polλ during short gap filling synthesis.
Enzyme | Mispair | # mutantsc | E.R.d×10−4 |
Polλ R438 a | T • dGTP | 6 | 2.5 |
T • dCTP | 0 | ≤0.4 | |
T • dTTP | 0 | ≤0.4 | |
G • dATP | 0 | ≤0.4 | |
G • dGTP | 0 | ≤0.4 | |
A • dCTP | 31 | 13 | |
A • dGTP | 1 | 0.4 | |
A • dATP | 1 | 0.4 | |
Polλ W438 b | T • dGTP | 26 | 10 |
T • dCTP | 0 | ≤0.4 | |
T • dTTP | 0 | ≤0.4 | |
G • dATP | 9 | 3.5 | |
G • dGTP | 0 | ≤0.4 | |
A • dCTP | 57 | 22 | |
A • dGTP | 3 | 1.2 | |
A • dATP | 0 | ≤0.4 |
Mutation Frequency (Polλ R438): 9.8×10−4.
Mutation Frequency (Polλ W438): 22.05×10−4.
Total sequenced: Polλ R438->42; Polλ W438->96.
The error rates are calculated based on sequencing mutants from two different reactions with each enzyme, and using the average mutant frequency for those two experiments, i.e., 9.8×10−4 and 22.05×10−4 for Polλ R438 and Polλ W438, respectively.