Table S1.
Primer set | Primer sequences, forward and reverse, 5′ to 3′ | R2 | Efficiency | Slope 95% confidence interval |
Drosophila | ||||
Intact | CGACAGCATTCCTGCGTAGTAAGA | 0.995 | 106.6% | −3.34 < s < −3.01 |
ACAATGCAAATTGCCCCTTA | ||||
Depurinated | CGACAGCATTCCTGCGTAGTAAGT | 0.997 | 101.4% | −3.44 < s < −3.13 |
ACAATGCAAATTGCCCCTTA | ||||
Normalizer | CAAGGACATTGCCAGGTAGG | 0.997 | 102.7% | −3.40 < s < −3.12 |
AGCTTTTGCTGTCCCTGTGT | ||||
Howardula | ||||
Intact | TGATAGTAATCCTGCTTAGTAAGA | 0.997 | 98.0% | −3.52 < s < −3.22 |
CACCGGAGAGCAACGATATT | ||||
Depurinated | TGATAGTAATCCTGCTTAGTAAGT | 0.998 | 105.4% | −3.32 < s < −3.08 |
CACCGGAGAGCAACGATATT | ||||
Normalizer | CAAATGCCTCGTCGGATG | 0.991 | 92.1% | −3.81 < s < −3.24 |
GCCAAAGCCTCCCACTTATAC | ||||
Rabbit | ||||
Intact | GGGTTTAGACCGTCGTGAGA | 0.998 | 79.6% | −4.03 < s < −3.83 |
AGTGGAACCGCAGGTTCAGA | ||||
Depurinated | GGGTTTAGACCGTCGTGAGA | 0.997 | 78.9% | −4.13 < s < −3.80 |
TGTGGAACCGCAGGTTCAGA | ||||
Normalizer | CGTTGGATTGTTCACCCACT | 0.999 | 96.4% | −3.48 < s < −3.33 |
CATACACCAAATGTCTGAACCTG |
Efficiency and specificity were validated on standard curves of 5 × 10-fold serial dilutions of synthetic DNA (IDT gBlocks) for all primer sets, except for the primer pair for the Howardula normalizing primer set, which was tested using a dilution series of cDNA reverse-transcribed from Howardula-infected flies. Bases specific to sites of depurination are in bold, and deliberate mismatches are underlined.