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. 2005 Nov 14;102(47):17059–17064. doi: 10.1073/pnas.0502974102

Table 1. Experimental groups.

Group Genotype Constructs injected No. harboring tumors (tumor multiplicity)
1 Arf –/– pT/Caggs-V12Nras + pPGK-SB13 8/8 (TNTC)
2 Arf –/– pT/Caggs-V12Nras + pPGK 4/7 (0–1)
3 Arf –/– pT/Caggs-V12A38Nras + pPGK-SB13 1/7* (NA)
4 Arf –/– pT2/Caggs-Luciferase + pPGK-SB13 0/5 (NA)
5 Arf +/– pT/Caggs-V12Nras + pPGK-SB13 7/8 (2–10)
6 Arf –/– pT/Caggs-V12S35Nras + pPGK-SB13 2/3 (1)
7 Arf –/– pT/Caggs-V12G37Nras + pPGK-SB13 0/3 (NA)

Each group received a different combination of transposon and transposase and was monitored for sickness. When moribund, liver tumor burden was assessed, and approximate numbers are indicated. TNTC, too numerous to count; NA, not applicable.

*

This mouse developed a different tumor type than the others

The third mouse died during the study and was not recovered