Skip to main content Accessibility help
×
Home
  • Get access
    Check if you have access via personal or institutional login
  • Cited by 7
  • Print publication year: 2012
  • Online publication date: August 2012

12 - The mouse t-haplotype:

References

Artzt, K., Shin, H. S., and Bennett, D. (1982). Gene mapping within the T/t complex of the mouse: II. Anomalous position of the H-2 complex in t haplotypes. Cell, 28, 471–6.
Bauer, H., Veron, N., Willert, J., and Herrmann, B. G. (2007). The t-complex-encoded guanine nucleotide exchange factor Fgd2 reveals that two opposing signaling pathways promote transmission ratio distortion in the mouse. Genes & Development, 21, 143–7.
Bauer, H., Willert, J. R., Koschorz, B., and Herrmann, B. G. (2005). The t complex-encoded GTPase-activating protein Tagap1 acts as a transmission ratio distorter in mice. Nature Genetics, 37, 969–73.
Bennett, D. (1975). T-locus of mouse. Cell, 6, 441–54.
Bennett, D. (1977). L. C. Dunn and his contribution to T-locus genetics. Annual Review of Genetics, 11, 1–12.
Bennett, D., Alton, A. K., and Artzt, K. (1983). Genetic analysis of transmission ratio distortion by t-haplotypes in the mouse. Genetical Research, 41, 29–45.
Chesley, P. and Dunn, L. C. (1936). The inheritance of taillessness (anury) in the house mouse. Genetics, 21, 525–36.
Ewulonu, U. K., Schimenti, K., Kuemerle, B., Magnuson, T., and Schimenti, J. (1996). Targeted mutagenesis of a candidate t complex responder gene in mouse t haplotypes does not eliminate transmission ratio distortion. Genetics, 144, 785–92.
Forejt, J. (1972). Chiasmata and crossing-over in the male mouse (Mus musculus): suppression of recombination and chiasma frequencies in the ninth linkage group. Folia Biologica, 18, 161–70.
Forejt, J., Čapková, J., and Gregorová, S. (1980). T(16: 17)43H translocation as a tool in analysis of the proximal part of chromosome 17 (including T-t gene complex) of the mouse. Genetical Research, 35, 165–77.
Fossella, J., Samant, S. A., Silver, L. M., et al. (2000). An axonemal dynein at the Hybrid Sterility 6 locus: implications for t haplotype-specific male sterility and the evolution of species barriers. Mammalian Genome, 11, 8–15.
Fox, H. S., Martin, G. R., Lyon, M. F., et al. (1985). Molecular probes define different regions of the mouse t complex. Cell, 40, 63–9.
Gummere, G. R., McCormick, P. J., and Bennett, D. (1986). The influence of genetic background and the homologous chromosome 17 on t-haplotype transmission ratio distortion in mice. Genetics, 114, 235–45.
Hammer, M. F., Schimenti, J., and Silver, L. M. (1989). Evolution of mouse chromosome 17 and the origin of inversions associated with t haplotypes. Proceedings of the National Academy of Sciences of the United States of America, 86, 3261–5.
Hammer, M. F. and SilverL. M. (1993). Phylogenetic analysis of the alpha-globin pseudogene-4 (Hba-ps4) locus in the house mouse species complex reveals a stepwise evolution of t haplotypes. Molecular Biology and Evolution, 10, 971–1001.
Hammerberg, C. (1981). The influence of TOrl upon male fertility in t-bearing mice. Genetical Research, 37, 71–7.
Hammerberg, C. (1982). The effects of the t-complex upon male reproduction are due to complex interactions between its several regions. Genetical Research, 39, 219–26.
Herrmann, B. G., Barlow, D. P., and Lehrach, H. (1987). A large inverted duplication allows homologous recombination between chromosomes heterozygous for the proximal t complex inversion. Cell, 48, 813–25.
Herrmann, B. G., Bucan, M., Mains, P. E., et al. (1986). Genetic analysis of the proximal portion of the mouse t complex: evidence for a second inversion within t haplotypes. Cell, 44, 469–76.
Herrmann, B. G., Koschorz, B., Wertz, K., et al. (1999). A protein kinase encoded by the t complex responder gene causes non-mendelian inheritance. Nature, 402, 141–6.
Herrmann, B. G., Labeit, S., Poustka, A., King, T. R., and Lehrach, H. (1990). Cloning of the T gene required in mesoderm formation in the mouse. Nature, 343, 617–22.
Katz, D. F., Erickson, R. P., and Nathanson, M. (1979). Beat frequency is bimodally distributed in spermatozoa from T/t12 mice. Journal of Experimental Zoology, 210, 529–35.
Klein, J., Sipos, P., and Figueroa, F. (1984). Polymorphism of t-complex genes in European wild mice. Genetical Research, 44, 39–46.
Korzh, V. and Grunwald, D. (2001). Nadine Dobrovolskaia-Zavadskaia and the dawn of developmental genetics. Bioessays, 23, 365–71.
Lader, E., Ha, H. S., O’Neill, M., Artzt, K., and Bennett, D. (1989) Tctex-1: a candidate gene family for a mouse T-complex sterility locus. Cell, 58, 969–79.
Lyon, M. F. (1956). Hereditary hair loss in the tufted mutant of the house mouse. Journal of Heredity, 47, 101–3.
Lyon, M. F. (1984). Transmission ratio distortion in mouse t-haplotypes is due to multiple distorter genes acting on a responder locus. Cell, 37, 621–8.
Lyon, M. F. (1986). Male sterility of the mouse t-complex is due to homozygosity of the distorter genes. Cell, 44, 357–63.
Lyon, M. F. (1992). Deletion of mouse t-complex distorter-1 produces an effect like that of the t-form of the distorter. Genetical Research, 59, 27–33.
Lyon, M. F. (2003). Transmission ratio distortion in mice. Annual Review of Genetics, 37, 393–408.
Lyon, M. F. and Mason, I. (1977). Information on the nature of t-haplotypes from the interaction of mutant haplotypes in male fertility and segregation ratio. Genetical Research, 29, 255–66.
Lyon, M. F. and Meredith, R. (1964a). Investigations of the nature of t-alleles in the mouse: I. Genetic analysis of a series of mutants derived from a lethal allele. Heredity, 19, 301–12.
Lyon, M. F. and Meredith, R. (1964b). Investigations of the nature of t-alleles in the mouse: II. Genetic analysis of an unusual mutant allele and its derivatives. Heredity, 19, 313–25.
Lyon, M. F. and Meredith, R. (1964c). Investigations of the nature of t-alleles in the mouse: III. Short tests of some further mutant alleles. Heredity, 19, 327–30.
Lyon, M. F., Schimenti, J. C., and Evans, E. P. (2000). Narrowing the critical regions for mouse t complex transmission ratio distortion factors by use of deletions. Genetics, 155, 793–801.
Morita, T., Kubota, H., Murata, K., et al. (1992). Evolution of the mouse t haplotype: recent and worldwide introgression to Mus musculus. Proceedings of the National Academy of Sciences of the United States of America, 89, 6851–5.
Olds-Clarke, P. and Johnson, L. R. (1993). t haplotypes in the mouse compromise sperm flagellar function. Developmental Biology, 155, 14–25.
Olds-Clarke, P. and Peitz, B. (1985). Fertility of sperm from t/+ mice: evidence that +-bearing sperm are dysfunctional. Genetical Research, 47, 49–52.
Planchart, A., You, Y., and Schimenti, J. C. (2000). Physical mapping of male fertility and meiotic drive quantitative trait loci in the mouse t complex using chromosome deficiencies. Genetics, 155, 803–12.
Rohme, D., Fox, H., Herrmann, B., et al. (1984). Molecular clones of the mouse t complex derived from microdissected metaphase chromosomes. Cell, 36, 783–8.
Rosen, L. L., Bullard, D. C., Silver, L. M., and Schimenti, J. C. (1990). Molecular cloning of the t complex responder genetic locus. Genomics, 8, 134–40.
Schimenti, J., Cebra-Thomas, J. A., Decker, C. L., et al. (1988). A candidate gene family for the mouse t complex responder (Tcr) locus responsible for haploid effects on sperm function. Cell, 55, 71–8.
Schimenti, J. C., Reynolds, J. L., and Planchart, A. (2005). Mutations in Serac1 or Synj2 cause proximal t haplotype-mediated male mouse sterility but not transmission ratio distortion. Proceedings of the National Academy of Sciences of the United States of America, 102, 3342–7.
Silver, L. M. (1989). Gene dosage effects on transmission ratio distortion and fertility in mice that carry t haplotypes. Genetical Research, 54, 221–5.
Silver, L. M., Hammer, M., Fox, H., et al. (1987). Molecular evidence for the rapid propagation of mouse t haplotypes from a single, recent, ancestral chromosome. Molecular Biology and Evolution, 4, 473–82.
Silver, L. M. and Olds-Clarke, P. (1984). Transmission ratio distortion of mouse t haplotypes is not a consequence of wild-type sperm degeneration. Developmental Biology, 105, 250–2.
Silver, L. M. and Remis, D. (1987). Five of the nine genetically defined regions of mouse t haplotypes are involved in transmission ratio distortion. Genetical Research, 49, 51–6.
Véron, N., Bauer, H., Weisse, A. Y., et al. (2009). Retention of gene products in syncytial spermatids promotes non-Mendelian inheritance as revealed by the t complex responder. Genes & Development, 23, 2705–10.
Willison, K. R., Dudley, K., and Potter, J. (1986). Molecular cloning and sequence analysis of a haploid expressed gene encoding t complex polypeptide 1. Cell, 44, 727–38.