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  • Print publication year: 2012
  • Online publication date: August 2012

19 - Hybrid male sterility genes in the mouse subspecific crosses

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Baudat, F., Buard, J., Grey, C., et al. (2010). PRDM9 is a major determinant of meiotic recombination hotspots in humans and mice. Science, 327, 836–40.
Bauer, H., Véron, 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.
Bayes, J. J. and Malik, H. S. (2009). Altered heterochromatin binding by a hybrid sterility protein in Drosophila sibling species. Science, 326, 1538–41.
Berg, I. L., Neumann, R., Lam, K. W., et al. (2010). PRDM9 variation strongly influences recombination hot-spot activity and meiotic instability in humans. Nature Genetics, 42, 859–63.
Bonhomme, F., Martin, S., and Thaler, L. (1978). Hybridization between Mus musculus L. and Mus spretus Lataste under laboratory conditions. Experientia, 34, 1140–1.
Boursot, P., Din, W., Anand, R., et al. (1996). Origin and radiation of the house mouse: mitochondrial DNA phylogeny. Journal of Evolutionary Biology, 9, 391–415.
Brayer, K. J. and Segal, D. J. (2008). Keep your fingers off my DNA: protein–protein interactions mediated by C2H2 zinc finger domains. Cell Biochemistry and Biophysics, 50, 111–31.
Brideau, N. J., Flores, H. A., Wang, J., et al. (2006). Two Dobzhansky–Muller genes interact to cause hybrid lethality in Drosophila. Science, 314, 1292–5.
Buard, J., Barthes, P., Grey, C., and de Massy, B. (2009). Distinct histone modifications define initiation and repair of meiotic recombination in the mouse. EMBO Journal, 28, 2616–24.
Cheung, V. G., Sherman, S. L., and Feingold, E. (2010). Genetic control of hotspots. Science, 327, 791–2.
Coop, G. and Myers, S. R. (2007). Live hot, die young: transmission distortion in recombination hotspots. PLoS Genetics, 3, e35.
Coyne, J. A. and Orr, H. A. (2004). Speciation. Sunderland, MA: Sinauer Associates.
Darwin, C. (1859). On the Origin of Species by Means of Natural Selection. London: John Murray.
Dobzhansky, T. (1951). Genetics and the Origin of Species. New York: Columbia University Press.
Elliott, R. W., Miller, D. R., Pearsall, R. S., et al. (2001). Genetic analysis of testis weight and fertility in an interspecies hybrid congenic strain for Chromosome X. Mammalian Genome, 12, 45–51.
Elliott, R. W., Poslinski, D., Tabaczynski, D., Hohman, C., and Pazik, J. (2004). Loci affecting male fertility in hybrids between Mus macedonicus and C57BL/6. Mammalian Genome, 15, 704–10.
Forejt, J. (1981). Hybrid sterility gene located in the T/t – H-2 supergene on chromosome 17. In Current Trends in Histocompatibility, ed. R. A. Reisfeld and S. Ferrone. New York: Plenum Press, pp. 103–31.
Forejt, J. (1982). X–Y involvement in male sterility caused by autosome translocations: a hypothesis. In Genetic Control of Gamete Production and Function, ed. M. Fraccaro and B. Rubin. New York: Academic Press, pp. 135–51.
Forejt, J. (1984). X-inactivation and its role in male sterility. In Chromosomes Today, ed. M. Bennett, A. Gropp, and U. Wolf. London: George Allen and Unwin, pp. 117–27.
Forejt, J. (1985). Chromosomal and genic sterility of hybrid type in mice and men. Experimental and Clinical Immunogenetics, 2, 106–19.
Forejt, J. (1996). Hybrid sterility in the mouse. Trends in Genetics, 12, 412–17.
Forejt, J., Gregorová, S., and Goetz, P. (1981). XY pair associates with the synaptonemal complex of autosomal male-sterile translocations in pachytene spermatocytes of the mouse (Mus musculus). Chromosoma, 82, 41–53.
Forejt, J. and Iványi, P. (1974). Genetic studies on male sterility of hybrids between laboratory and wild mice (Mus musculus L.). Genetical Research, 24, 189–206.
Forejt, J., Vincek, V., Klein, J., Lehrach, H., and Loudová-Micková, M. (1991). Genetic mapping of the t-complex region on mouse chromosome 17 including the Hybrid sterility-1 gene. Mammalian Genome, 1, 84–91.
Fossella, J., Samant, S., Silver, L., 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.
Geraldes, A., Basset, P., Gibson, B., et al. (2008). Inferring the history of speciation in house mice from autosomal, X-linked, Y-linked and mitochondrial genes. Molecular Ecology, 17, 5349–63.
Good, J. M., Dean, M. D., and Nachman, M. W. (2008a). A complex genetic basis to X-linked hybrid male sterility between two species of house mice. Genetics, 179, 2213–28.
Good, J. M., Giger, T., Dean, M. D., and Nachman, M. W. (2010). Widespread over-expression of the X chromosome in sterile F1 hybrid mice. PLoS Genetics, 6, e1001148.
Good, J. M., Handel, M. A., and Nachman, M. W. (2008b). Asymmetry and polymorphism of hybrid male sterility during the early stages of speciation in house mice. Evolution, 62, 50–65.
Gregorová, S., Divina, P., Storchová, R., et al. (2008). Mouse consomic strains: exploiting genetic divergence between Mus m. musculus and Mus m. domesticus subspecies. Genome Research, 18, 509–15.
Gregorová, S. and Forejt, J. (2000). PWD/Ph and PWK/Ph inbred mouse strains of Mus m. musculus subspecies: a valuable resource of phenotypic variations and genomic polymorphisms. Folia Biologica (Praha), 46, 31–41.
Gregorová, S., Mnuková-Fajdelová, M., Trachtulec, Z., et al. (1996). Sub-milliMorgan map of the proximal part of mouse Chromosome 17 including the hybrid sterility 1 gene. Mammalian Genome, 7, 107–13.
Grey, C., Baudat, F., and de Massy, B. (2009). Genome-wide control of the distribution of meiotic recombination. PLoS Biology, 7, e1000035.
Guénet, J. L. (2005). The mouse genome. Genome Research, 15, 1729–40.
Guénet, J. L, Nagamine, C., Simon-Chazottes, D., Montagutelli, X., and Bonhomme, F. (1990). Hst-3: an X-linked hybrid sterility gene. Genetical Research, 56: 163–5.
Haldane, J. (1922). Sex ratio and unisexual sterility in animal hybrids. Journal of Genetics, 12, 101–9.
Handel, M. A. and Schimenti, J. C. (2010). Genetics of mammalian meiosis: regulation, dynamics and impact on fertility. Nature Reviews Genetics, 11, 124–36.
Hayashi, K. and Matsui, Y. (2006). Meiosis-specific histone methylation is essential for meiotic progression. Tanpakushitsu Kakusan Koso, 51, 441–5.
Hayashi, K., Yoshida, K., and Matsui, Y. (2005). A histone H3 methyltransferase controls epigenetic events required for meiotic prophase. Nature, 438, 374–8.
Herrmann, B. G., Koschorz, B., Wertz, K., McLaughlin, K. J., and Kispert, A. (1999). A protein kinase encoded by the t complex responder gene causes non-Mendelian inheritance. Nature, 402, 141–6.
Hochwagen, A. and Marais, G. A. B. (2010). Meiosis: a PRDM9 guide to the hotspots of recombination. Current Biology, 20, R271–4.
Howell, G. R., Munroe, R. J., and Schimenti, J. C. (2005). Transgenic rescue of the mouse t complex haplolethal locus Thl1. Mammalian Genome, 16, 838–46.
Iványi, P., Vojtísková, M., Démant, P., and Micková, M. (1969). Genetic factors in the ninth linkage group influencing reproductive performance in male mice. Folia Biologica (Praha), 15, 401–21.
Lu, X., Shapiro, J. A., Ting, C.-T., et al. (2010). Genome-wide misexpression of X-linked versus autosomal genes associated with hybrid male sterility. Genome Research, 20, 1097–102.
Lyon, M. F. (2003). Transmission ratio distortion in mice. Annual Review of Genetics, 37, 393–408.
Macholán, M., Baird, S. J. E., Dufková, P., et al. (2011). Assessing multilocus introgression patterns: a case study on the mouse X chromosome in Central Europe. Evolution, 65, 1428–46.
Macholán, M., Munclinger, P., Šugerková. M., et al. (2007). Genetic analysis of autosomal and X-linked markers across a mouse hybrid zone. Evolution, 61, 746–71.
Maheshwari, S., Wang, J., and Barbash, D. A. (2008). Recurrent positive selection of the Drosophila hybrid incompatibility gene Hmr. Molecular Biology and Evolution, 25, 2421–30.
Masly, J. P., Jones, C. D., Noor, M. A., Locke, J., and Orr, H. A. (2006). Gene transposition as a cause of hybrid sterility in Drosophila. Science, 313, 1448–50.
Matsuda, Y., Hirobe, T., and Chapman, V. M. (1991). Genetic basis of X–Y chromosome dissociation and male sterility in interspecific hybrids. Proceedings of the National Academy of Sciences of the United States of America, 88, 4850–4.
Mihola, O., Forejt, J., and Trachtulec, Z. (2007). Conserved alternative and antisense transcripts at the programmed cell death 2 locus. BMC Genomics, 8, 20.
Mihola, O., Trachtulec, Z., Vlcek, C., Schimenti, J. C., and Forejt, J. (2009). A mouse speciation gene encodes a meiotic histone H3 methyltransferase. Science, 323, 373–5.
Muller, H. J. (1942). Isolating mechanisms, evolution, and temperature. Biological Symposia, 6, 71–125.
Myers, S., Bowden, R., Tumian, A., et al. (2010). Drive against hotspot motifs in primates implicates the PRDM9 gene in meiotic recombination. Science, 327, 876–9.
Neale, M. J. (2010). PRDM9 points the zinc finger at meiotic recombination hotspots. Genome Biology, 11, 104.
Oka, A., Aoto, T., Totsuka, Y., et al. (2007). Disruption of genetic interaction between two autosomal regions and the X chromosome causes reproductive isolation between mouse strains derived from different subspecies. Genetics, 175, 185–97.
Oka, A., Mita, A., Sakurai-Yamatani, N., et al. (2004). Hybrid breakdown caused by substitution of the X chromosome between two mouse subspecies. Genetics, 166, 913–24.
Oka, A., Mita, A., Takada, Y., Koseki, H., and Shiroishi, T. (2010). Reproductive isolation in hybrid mice due to spermatogenesis defects at three meiotic stages. Genetics, 186, 339–51.
Oliver, P. L., Goodstadt, L., Bayes, J. J., et al. (2009). Accelerated evolution of the Prdm9 speciation gene across diverse metazoan taxa. PLoS Genetics, 5, e1000753.
Paigen, K. and Petkov, P. (2010). Mammalian recombination hot spots: properties, control and evolution. Nature Reviews Genetics, 11, 221–33.
Parvanov, E. D., Ng, S. H. S., Petkov, P. M., and Paigen, K. (2009). Trans-regulation of mouse meiotic recombination hotspots by Rcr1. PLoS Biology, 7, e1000036.
Parvanov, E. D., Petkov, P. M., and Paigen, K. (2010). Prdm9 controls activation of mammalian recombination hotspots. Science, 327, 835.
Phadnis, N. and Orr, H. A. (2009). A single gene causes both male sterility and segregation distortion in Drosophila hybrids. Science, 323, 376–9.
Piálek, J., Vyskočilová, M., Bímová, B., et al. (2008). Development of unique house mouse resources suitable for evolutionary studies of speciation. Journal of Heredity, 99, 34–44.
Pilder, S. H., Hammer, M. F., and Silver, L. M. (1991). A novel mouse chromosome 17 hybrid sterility locus: implications for the origin of t haplotypes. Genetics, 129, 237–46.
Pilder, S. H., Olds-Clarke, P., Orth, J. M., Jester, W. F., and Dugan, L. (1997). Hst7: a male sterility mutation perturbing sperm motility, flagellar assembly, and mitochondrial sheath differentiation. Journal of Andrology, 18, 663–71.
Pilder, S. H., Olds-Clarke, P., Phillips, D. M., and Silver, L. M. (1993). Hybrid sterility-6: a mouse t complex locus controlling sperm flagellar assembly and movement. Developmental Biology, 159, 631–42.
Presgraves, D. C. (2010). Darwin and the origin of interspecific genetic incompatibilities. American Naturalist, 176(S1), S45–60.
Reed, L. K., LaFlamme, B. A., and Markow, T. A. (2008). Genetic architecture of hybrid male sterility in Drosophila: analysis of intraspecies variation for interspecies isolation. PLoS ONE, 3, e3076.
Reed, L. K. and Markow, T. A. (2004). Early events in speciation: polymorphism for hybrid male sterility in Drosophila. Proceedings of the National Academy of Sciences of the United States of America, 101, 9009–12.
Sandovici, I. and Sapienza, C. (2010). PRDM9 sticks its zinc fingers into recombination hotspots and between species. F1000 Biology Reports, 2, 37.
She, J. X., Bonhomme, F., Boursot, P., Thaler, L., and Catzeflis, F. (1990). Molecular phylogenies in the genus Mus: comparative analysis of electrophoretic, scnDNA hybridization, and mtDNA RFLP data. Biological Journal of the Linnean Society, 41: 83–103.
Storchová, R., Gregorová, S., Buckiová, D., et al. (2004). Genetic analysis of X-linked hybrid sterility in the house mouse. Mammalian Genome, 15, 515–24.
Teeter, K. C., Payseur, B. A., Harris, L. W., et al. (2008). Genome-wide patterns of gene flow across a house mouse hybrid zone. Genome Research, 18, 67–76.
Teeter, K. C., Thibodeau, L. M., Gompert, Z., et al. (2010). The variable genomic architecture of isolation between hybridizing species of house mice. Evolution, 64, 472–85.
Thomas, J. H., Emerson, R. O., and Shendure, J. (2009). Extraordinary molecular evolution in the PRDM9 fertility gene. PLoS ONE, 4, e8505.
Ting, C.-T., Tsaur, S.-C., Wu, M.-L., and Wu, C.-I. (1998). A rapidly evolving homeobox at the site of a hybrid sterility gene. Science, 282, 1501–4.
Trachtulec, Z., Mihola, O., Vlcek, C., et al. (2005). Positional cloning of the hybrid sterility 1 gene: fine genetic mapping and evaluation of two candidate genes. Biological Journal of the Linnean Society, 84, 637–41.
Trachtulec, Z., Mnuková-Fajdelová, M., Hamvas, R., et al. (1997). Isolation of candidate hybrid sterility 1 genes by cDNA selection in a 1.1 megabase pair region on mouse chromosome 17. Mammalian Genome, 8, 312–16.
Trachtulec, Z., Vincek, V., Hamvas, R., et al. (1994). Physical map of mouse chromosome 17 in the region relevant for positional cloning of the Hybrid sterility 1 gene. Genomics, 23, 132–7.
Trachtulec, Z., Vlcek, C., Mihola, O., et al. (2008). Fine haplotype structure of a chromosome 17 region in the laboratory and wild mouse. Genetics, 178, 1777–84.
Turelli, M. and Orr, H. A. (2000). Dominance, epistasis and the genetics of postzygotic isolation. Genetics, 154, 1663–79.
Turner, J. M. A. (2007). Meiotic sex chromosome inactivation. Development, 134, 1823–31.
Vyskočilová, M., Pražanová, G., and Piálek, J. (2009). Polymorphism in hybrid male sterility in wild-derived Mus musculus musculus strains on proximal chromosome 17. Mammalian Genome, 20, 83–91.
Vyskočilová, M., Trachtulec, Z., Forejt, J., and Piálek, J. (2005). Does geography matter in hybrid sterility in house mice?Biological Journal of the Linnean Society, 64, 663–74.