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. 2012 Apr 24;29(10):2997–3004. doi: 10.1093/molbev/mss119

Table 1.

Nucleotide Changes and Frequencies in Three Adapted Codon-Modified Lines.

Line (frequencya)
Position Base Change AA Change Gene (function) S1 S2 L1
4303 A →G k 378 r 1 (RNAP) 0.115
3664 A → C n 165 t 1 0.214
9158 A → T m 1 mb 2.5 (ssDNA binding) 0.389
14204 G → A g 93 d 4.7 (DNA metabolism) 0.196
14279 T → C i 118 t 4.7 0.528
17766 T → C v 88 a 6 (exonuclease) 0.200
23129 A → G i 55 v 10A (major capsid) 0.438 0.114
23131 A → C i 55 i 10A 0.350 0.100 0.891
23425 T → C n 153 n 10A 0.188
23431 T → C n 155 n 10A 0.172
23434 A → C i 156 i 10A 0.111
A → G i 156 m 10A 0.500
24088 G → A e 375 k 10B (major capsid) 0.720
24106 G → A a 361 t 10B 0.406
26984 A → C t 715 p 12 (internal virion) 0.429
36052 A → C s 477 r 17 (tail fiber) 0.158
38307 T → C l 313 s 19 (terminase) 0.125

NOTE.—A polymorphic, silent G → A change in gene 17 (base 35772, codon 383) was observed in all lines at a frequency of ∼0.4 relative to the wild-type base. This change was even observed in the initial T710A0.1 which was recently derived from a clonal isolate. We suspect that this change is a sequencing artefact and omit it from the table and our discussion of evolution in these lines.

a

To be reported here, the frequency of a nucleotide change had to reach 0.1 and be observed in at least two reads.

b

Change to a UUG start codon.