References
Artzt, K., Shin, H.-S., and Bennett, D.: Gene mapping within the T/t-complex of the mouse. II. Anomalous position of the H-2 complex in t-haplotypes. Cell 28: 471–476, 1982.
Bullard, D.C. and Schimenti, J.C.: Molecular cloning and genetic mapping of the t complex responder candidate gene family. Genetics 124: 957–966, 1990.
Cannizzarro, L.A. and Emanuel, B.E.: An improved method for G-banding chromosomes after in situ hybridization. Cytogenet Cell Genet 38: 308–309, 1984.
Cebra-Thomas, J.A., Decker, C., Snyder, L.C., Pilder, S.H., and Silver, L.M.: Allele- and haploid-specific product generated by alternative splicing from a mouse t complex responder locus candidate. Nature 349: 239–241, 1991.
Committee for Mouse Chromosome 17 {Artzt, K., Barlow, D., Dove, W.F., Fischer-Lindahl, K., Klein, J., Lyon, M.F., and Silver, L.M.}: Maps of mouse chromosome 17: First report. Mammalian Genome 1: 5–29, 1991.
Committee for the Standardized Genetic Nomenclature for Mice.: Standard karyotype of the mouse Mus musculus. J Heredity 63: 69–72, 1972.
Dudley, K., Shanahan, F., Burtenshaw, M., Evans, E.P., Ruddy, S., and Lyon, M.F.: Isolation and characterization of a cDNA clone corresponding to the mouse t-complex gene Tcp-1x. Genet Res 57: 147–152, 1991.
Feinberg, A.P. and Vogelstein, B.: A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity. Anal Biochem 137: 266–267, 1984.
Hammer, M.F., Schimenti, J., and Silver, L.M.: Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes. Proc Natl Acad Sci USA 86: 3261–3265, 1989.
Harper, M.E., Ullrich, A., and Saunders, G.F.: Localization of the human insulin gene to the distal end of the short arm of chromosome 11. Proc Natl Acad Sci USA 78: 4458–4460, 1981.
Lader, E., Clark, B.T., Jhanwar, S.C., Chaganti, R.S.K., and Bennett, D.: Definitive chromosomal location of the H-2 complex by in situ hybridization to pachytene chromosomes. Immunogenetics 22: 49–54, 1985.
Lichter, P., Tang, C.-J., Call, K., Hermanson, G., Evans, G.A., Housman, D., and Ward, D.C.: High resolution mapping of human chromosome 11 by in situ hybridization with cosmid clones. Science 247: 64–69, 1990.
Lyon, M.F., Zenthon, J., Evans, E.P., Burtenshaw, M.D., Dudley, K., and Willson, K.R.: Location of the t complex on mouse chromosome 17 by in situ hybridization with Tcp-1. Immunogenetics 24: 125–127, 1986.
Lyon, M.F., Zenthon, J., Evans, E.P., Burtenshaw, M.D., and Willison, K.R.: Extent of the mouse t complex and its inversions shown by in situ hybridization. Immunogenetics 27: 375–382, 1988.
Mazarakis, N.D., Nelki, D., Lyon, M.F., Ruddy, S., Evans, E.P., Freemont, P., and Dudley, K.: Isolation and characterization of a testis-expressed developmentally regulated gene from the distal inversion of the mouse t-complex. Development 111: 561–571, 1991.
Rosen, L.L., Bullard, D.C., Silver, L.M., and Schimenti, J.C.: Molecular cloning of the t complex responder genetic locus. Genomics 8: 134–140, 1990.
Sarvetnick, N., Tsai, J.-Y., Fox, H., Pilder, S.H., and Silver, L.M.: A mouse chromosome 17 gene encodes a testis-specific transcript with unusual properties. Immunogenetics 30: 34–41, 1989.
Schimenti, J., Cebra-Thomas, J.A., Decker, C., Islam, S., Pilder, S.H., and Silver, L.M.: A candidate gene family for the mouse t complex responder (Tcr) locus responsible for haploid effects on sperm function. Cell 55: 71–78, 1988.
Smiley, J.R., Steege, D.A., Juricek, D.K., Summers, W.P., and Ruddle, F.H.: A herpes simplex virus 1 integration site in the mouse genome defined by somatic cell genetic analysis. Cell 15: 455–468, 1978.
Threadgill, D.W., Wilkemeyer, M., Womack, J.E., and Ledley, F.D.: Localization of the murine methylmalonyl CoA mutase (Mut) locus on chromosome 17 by in situ hybridization. Cytogenet Cell Genet 53: 112–114, 1990.
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Mancoll, R.E., Snyder, L.C. & Silver, L.M. Delineation of the t complex on mouse Chromosome 17 by in situ hybridization. Mammalian Genome 2, 201–205 (1992). https://doi.org/10.1007/BF00302878
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DOI: https://doi.org/10.1007/BF00302878