Abstract
The genetic basis of congenital transmission of mammary tumor virus (MTV) by GR females was studied with F1 F2, and backcross populations of GR X BALB/c (C-) mice. All mice were foster-nursed by MTV-free C- mothers. The occurrence of 1 or more of the 3 kinds of mammary lesions (pregnancy-dependent tumors, pregnancy-independent tumors or hyperplastic nodules) in force-bred females within the first year was considered an indication of MTV infection. A mouse without mammary lesions was still considered MTV-infected if she transmitted MTV through her milk. One hundred percent of reciprocal F1 hybrids developed mammary tumors by 7 months, and the incidence of mammary tumors in (GR × C-) × GR backcrosses was also close to 100%. From the criteria used to determine MTV infection, 75% of the (GR × C-) × GR backcross females were MTV-infected. Although mammary lesions were detected in only 77% of the F2:[(GR × C-) × (GR × C-) populations, some lesion-free mice also transmitted MTV by milk. It was predicted that at least 90% of the F2 females were likely to be infected with MTV. The ratios of MTV-infected females in F1 F2, and backcross populations appeared compatible with the hypothesis that 2 independently segregating dominant genes in the GR mouse strain are involved in congenital transmission of its MTV, and that either one of these genes alone is adequate for MTV transmission.