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. 2002 Feb 26;99(6):3770–3775. doi: 10.1073/pnas.052710299

Table 1.

λ cII mutant frequencies in mammary glands and tumors

Mouse ID Age (months) Mammary glands
Mammary tumors
Total pfu × 103 Mutant plaques Mutant frequency × 10−5 Total pfu × 103 Mutant plaques Mutant frequency × 10−5
neu-1 19 381 56 14.7 280 98 35.0
neu-2 19 274 42 15.3 188 72 38.3
neu-3 20 220 60 27.3 288 123 42.7
neu-4 20 263 63 24.0
neu-5 23 272 54 19.8 285 98 34.4
neu-6 23 178 82 46.1
neu-7 17 184 25 13.6
neu-8 23 233 50 21.7 164 180 31.7
neu-9 24 223 38 17.0 192 56 29.2
neu-10 25 234 42 18.0
neu-11 25 102 21 20.7 443 64 14.4
Mean ± SEM 19.5 ± 2.1  29.8 ± 3.3 
wt-1 6.0 144 21 14.6
wt-2 4.5 523 98 18.7
wt-3 4.0 220 29 13.2
wt-4 4.0 243 26 10.7
wt-5 5.5 157 17 10.8
wt-6 4.0 148 19 12.8
wt-7 5.5 142 18 12.7
Mean ± SEM 13.4 ± 1.0 

Tissues are derived from: (neu-1 through neu-11) ErbB2/Big Blue bitransgenic mice carrying both the MMTV-c-erbB2 transgene and a second transgene consisting of multiple copies of the λ bacteriophage genome; or (wt-1 through wt-7) phenotypically wild-type Big Blue single transgenic mice crossed once to FVB/N mice. Note that although the wild-type group was substantially younger than the bitransgenic group, contralateral “normal” mammary tissues from seven tumor-bearing ErbB2/Big Blue bitransgenic mice were subjected to cII mutation analyses and their collective mutant frequency was significantly lower than the frank tumors (P < 0.05).