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. 2011 Apr 15;3(4):398–422. doi: 10.3390/v3040398

Table 1.

Common insertion sites (CIS) or activated proto-oncogenes in MuLV-induced tumors1.

VIRUS DISEASE CIS or PROTO-ONCOGENE
Moloney MuLV T-lymphoma
In mice:
c-myc, pim-1, pvt-1/mis-1/mlvi-1, lck, pim-2a, n-myca, bmi-1a, frat-1a, pal-1/gfi-1a
In rats:
c-myc, pvt-1/mis-1/mlvi-1, mlvi-2, mlvi-3, mlvi-4, dsi-1, lck, tpl-1/ets-1a, tpl-2a, gfi-1/pal-1a, gfi-2/IL-9R
Myeloid leukemia c-myb, mml-1
AKR MuLV/Gross Virus; SL3-3 MuLV T-lymphoma c-myc, gin-1, n-ras
RadLV (Radiation leukemia virus) T-lymphoma c-myc, pim-1, vin-1/cyclinD2, notch1, kis-1, kis-2
Friend MuLV Erythroleukemia fli-1, fre-2
Myeloid leukemia fis-1, fim-1, evi-1/fim-3, c-fms/fim-2
Endogenous MuLV (AKXD, BXH-2 recombinant inbred mice) Myeloid leukemia evi-1/fim-3, evi-2, meis-1 and others1
B-lymphoma evi-3 and others1
Abelson MuLV (contains v-abl oncogene) B-lymphoma ahi-1, ahi-2 (M-MuLV helper inserted)
Friend SSFV (SFFV gp52c is an oncogene) Erythroleukemia Spi-1, p53b
1

Data from retroviral tagging of mice genetically predisposed to cancer (e.g., myc transgenic mice) are not included here. They can be found in the Mouse Retrovirus Tagged Cancer Gene (RTCG) database [65,66].

a

Insertions associated with tumor progression or that collaborate with other proto-oncogene activations;

b

Insertion at p53 inactivates its function;

c

gp52 oncogene is a deleted form of endogenous retroviral envelope protein.