Testicular teratomas can be experimentally induced in some strains of mice by grafting 12- or 13-day male genital ridges to the testes of adults. The grafts develop into testes and teratomas can be recognized histologically in them about a week after grafting. Some strains are more susceptible to experimental teratocarcinogenesis than others, and strains 129 and A/He are more susceptible than any others tested. F1 hybrids between these strains are even more susceptible than either parent strain. This suggested that strain A/He may have a gene or genes lacking in strain 129 that influence susceptibility to experimental teratocarcinogenesis. To test this hypothesis we made several recombinant inbred (RI) strains using strains 129 and A/He as progenitors. Each of the RI strains should have half of its genes derived from one progenitor and half from the other, and each RI strain should have a different combination of fixed genes. Nine strains have been inbred for more than twenty generations of brother times sister matings. Four of these new RI strains are more susceptible to experimental teratocarcinogenesis than either parent strain, three are less susceptible, and two are about the same. This indicates that some of the genes that determine susceptibility are the same in both parent strains. It also indicates that strain A/He has a gene or genes lacking in strain 129 that increases susceptibility to experimental teratocarcinogenesis. Reciprocal crosses were made between RI lines and between RI lines and the parental strains. There was no evidence for a maternal influence on the inheritance of susceptibility. Even though some RI strains are highly susceptible to experimental teratocarcinogenesis, they rarely if ever have spontaneous teratomas. A recently identified gene, named teratoma (ter), dramatically increases the incidence of teratomas in strain 129 mice. It also causes teratomas in the susceptible RI strains. (M)

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA002662-31
Application #
3163093
Study Section
(SSS)
Project Start
1976-09-01
Project End
1986-08-31
Budget Start
1985-09-01
Budget End
1986-08-31
Support Year
31
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Jackson Laboratory
Department
Type
DUNS #
042140483
City
Bar Harbor
State
ME
Country
United States
Zip Code
Walt, H; Oosterhuis, J W; Stevens, L C (1993) Experimental testicular germ cell tumorigenesis in mouse strains with and without spontaneous tumours differs from development of germ cell tumours of the adult human testis. Int J Androl 16:267-71
Taketo, M; Schroeder, A C; Mobraaten, L E et al. (1991) FVB/N: an inbred mouse strain preferable for transgenic analyses. Proc Natl Acad Sci U S A 88:2065-9
Muntener, M; Kagi, U; Stevens, L C et al. (1990) Innervation and maturation of muscular tissue in testicular teratomas in strain 129/Sv-ter mice. Virchows Arch B Cell Pathol Incl Mol Pathol 59:223-9