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. 2003 Jul;77(14):7924–7935. doi: 10.1128/JVI.77.14.7924-7935.2003

TABLE 2.

Transforming activities of JSRV and ENTV Env YXXM mutants in NIH 3T3 cells during prolonged culturea

Env protein Transformed foci per dish at week:
2 3 4 5
Jenv-FLAG 18 ± 3.6 34 ± 10 TMTC
Jenv-Y590F-FLAG 0 1.5 ± 0.7 3 ± 2.6 5 ± 3.1
Jenv-Y590D-FLAG 0 1 ± 0 1 ± 0 1.5 ± 0.6
Jenv-Y590C-FLAG 0 0 1.5 ± 0.6 2.6 ± 0.6
Jenv-M593A-FLAG 8 ± 3.6 15 ± 4.5 24 ± 2.8 TMTC
Jenv-M593T-FLAG 6 ± 1.4 10 ± 4.7 14 ± 8.5 TMTC
Jenv-M593E-FLAG 0 0 0 3 ± 1.5
FLAG-Eenv 26 ± 8.7 47 ± 17 TMTC
FLAG-Eenv-Y590F 14 ± 3.2 26 ± 2.1 TMTC
FLAG-Eenv-Y590,2,6F 2 ± 0.7 2.5 ± 0.7 6 ± 2.5 6 ± 3
10A1 Env 0 0 0 0
a

NIH 3T3 cells were transfected with 10 μg of each plasmid encoding the indicated Env proteins. The next day, cells were split 1:2 into 6-cm dishes in medium containing G418 (750 μg/ml, active concentration). After 7 to 10 days of drug selection, cells were fed with DMEM plus 5% FBS every 3 to 4 days, and transformed foci were counted at the indicated times (foci per 5 μg of DNA). Results are means ± standard deviations of two independent experiments. TMTC, too many to count.