Table 1.
Mutation | No. of detectable mutations | Mutation rate (×10−7)* | Percentage of total |
Base substitutions | |||
GC to AT | 139 | 1,100 | 73 |
GC to TA | 24 | 190 | 12 |
GC to CG | 1 | 8.0 | 0.5 |
AT to GC | 14 | 110 | 8 |
AT to CG | 4 | 32 | 2 |
AT to TA | 7 | 56 | 4 |
−1 frameshift | 1 | 8.0 | 0.5 |
Total | 190 | 1,500 | 100 |
The data are based on DNA sequence analysis of 189 independent CanR mutants of msh6Δ pol3-R696W strains containing pPOL3. Fourteen mutants contained two different point mutations in the CAN1 gene. For these mutants, only mutations previously reported to produce a detectable CanR phenotype are shown; the others were identified as likely hitchhiker mutations and were excluded from the mutation rate calculation. The location of mutations in the CAN1 sequence is shown in Fig. S1.
The rate for each type of mutation was calculated as follows: MRi = (Mi/MT) × MR, where Mi is the number of mutations of the particular type, MT is the total number of mutations, and MR is the rate of CanR mutation in msh6Δ pol3-R696W strains containing pPOL3 as determined by fluctuation analysis (1,500 × 10−7; Table S1).