Abstract
Thirteen new congenic lines have been produced which have chromosome-7 segments introduced from different strains onto the C57BL/10Sn background. Sublines B10.P(61NX)C,D, and E received chromosome-7 segments from P/J, B10.CE(62NX) from CE/J, B10.SEC(64NX)A,C,E, and F from SEC/1Re, B10.SM(65NX) from SM/J, B10.WB(66NX) from WB/Re, B10.A(67NX) from A/SnGrf, B10.AKR(68NX) from AKR/SnGrf, and B10.K(69NX) from C3H.K. Isograft testing indicated that three sublines, B10.P(61NX)D, B10.CE(62NX)B, and B10.WB(66NX)B are histoisogenic, i.e., histocompatible within each line. With the exception of B10.A(67NX), B10.AK(68NX), and B10.K(69NX), which have not been isografted, the remaining sublines showed residual heterozygosity on isografting. The three histoisogenic lines have undergone F1 testing and have been found to possess theH-4 a allele and new and distinct alleles at theH-1 locus. They have been designated B10.P(61NX)-H-4a H-1 d, B10.WB(66NX)-H-4a H-1 e, and B10.CE(62NX)-H-4a H-1 f. Direct exchange of grafts has indicated the following genotypes: B10.A(67NX)-H-4a H-1 b, B10.AK(68NX)-H-4a H-1 b, and B10.K(69NX)-F-4a H-1 b. The B10.SEC(64NX) and B10.SM(65NX) sublines have not been typed completely forH-4 andH-1. F 1 testing or direct exchange of skin grafts indicated that B10.P(61NX)-H-4a H-1 d, B10.WB(66NX)-H-4a H-1 e, B10.A(67NX)-H-4a H-1 b B10.AK(68NX)-H-4a H-1 b and B10.K(69NX)-H-4a H1 b possess nonon-H-1 histocompatibility differences from the G57BL/10 background.
Similar content being viewed by others
References
Archer, J. R.: Inheritance of the macrophage alloantigenic marker (Mph-1) in inbred mice.Genet. Res. 26:213–219, 1975
Bailey, D. W.and Mobraaten, L. E.: Estimates of the number of loci contributing to the histoincompatibility between strains C57BL/6 and BALB/c.Transplantation 7:394–400, 1969
Bailey, D. W.: Histocompatibility in mice I. New Loci and Congenic Lines.Immunogenetics 2:249–256, 1975
Chapman, V. M., Nichols, E. A., and Ruddle, F. H.: Esterase-8(Es-8).Biochem. Genet. 11: 347–358, 1974
DeLorenzo, R. J. and Ruddle, F. H.: Genetic control of two electrophoretic varients of glucosephosphate isomerace in the mouse.Biochem. Genet. 3:151–162, 1969
Graff, R. J. and Snell, G. D.: Histocompatibility genes of mice VIII. The alleles of theH-1 locus.Transplantation 6:598–617, 1968
Graff, R. J. and Brown, D. H.: Estimate of H differences between and within inbred mouse strains.Immunogenetics 7:367–373, 1978
Rowe, W. P.: Genetic factors in the natural history of murine leukemia virus.Cancer Res. 33:3061–3068, 1973
Russell, E. S. and McFarland, E. C.: Genetics of mouse hemoglobins.Ann. N.Y. Acad. Sci. 241:25–38, 1914
Shows, T. B., Chapman, V. M., and Ruddle, T. H.: Mitochondrial malate dehydrogenase and malic enzyme.Biochem. Genet. 4:707–718, 1970
Snell, G. D. and Kelton, D.:H-l, a new first chromosome locus in the mouse.Proc. Am. Assoc. Cancer Res. 1:53–54, 1953
Snell, G. D. and Stevens, C. C.: Histocompatibility genes of mice III.H-1 andH-4, two histocompatibility loci in the first linkage group.Immunology 4:366–379, 1961
Snell, G. D., Dausset, J., and Nathenson, S.:Histocompatibility, pp. 401, Academic Press, New York, 1976
Stockert, E., Boyse, E. A., Sato, H., and Itakura, K.: Heredity of the GIX thymocyte antigen associated with murine leukemia virus.Proc. Natl. Acad. Sci. U.S.A. 73:2077, 1976
Van Nie, R. and Verstraeten, A. A.: Studies of genetic transmission of mammary tumor virus by C3Hf mice.Int. J. Cancer 16:922–931, 1975
Zink, G. L. and Heyner, S.: Further studies on non-H-2 alloantibodies in the mouse.Immunogenetics 6:269–276, 1978
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Graff, R.J., Brown, D.H. & Snell, G.D. Thirteen new chromosome-7 congenic lines. Immunogenetics 8, 245–256 (1979). https://doi.org/10.1007/BF01561434
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF01561434