Hybrid male sterility genes in the mouse subspecific crosses

Evolution of the House Mouse

Volumn , Issue , 2012, Pages 482-503

  Forejt, Jiří ^a   Piálek, Jaroslav ^b   Trachtulec, Zdenìk ^a  

^a INSTITUTE OF MOLECULAR GENETICS   (Czech Republic)

^b INSTITUTE OF VERTEBRATE BIOLOGY   (Czech Republic)

Author keywords

[No Author keywords available]

Indexed keywords

EID: 84870659174     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1017/CBO9781139044547.021     Document Type: Chapter

References (85)

1. 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.
2. 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.
3. Bayes, J. J. and Malik, H. S. (2009). Altered heterochromatin binding by a hybrid sterility protein in Drosophilasibling species. Science,326, 1538-41.
4. 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.
5. Bonhomme, F., Martin, S., and Thaler, L. (1978). Hybridization between Mus musculusL. and Mus spretusLataste under laboratory conditions. Experientia,34,1140-1.
6. 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.
7. 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.
8. 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.
9. 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.
10. Cheung, V. G., Sherman, S. L., and Feingold, E. (2010). Genetic control of hotspots. Science, 327 791-2.
11. Coop, G. and Myers, S. R. (2007). Live hot, die young: transmission distortion in recombination hotspots. PLoS Genetics,3, e35.
12. Coyne, J. A. and Orr, H. A. (2004). Speciation. Sunderland, MA: Sinauer Associates.
13. Darwin, C. (1859). On the Origin of Species by Means of Natural Selection. London: John Murray.
14. Dobzhansky, T. (1951). Genetics and the Origin of Species. NewYork: Columbia University Press.
15. 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.
16. Elliott, R. W., Poslinski, D., Tabaczynski, D., Hohman, C., and Pazik, J. (2004). Loci affecting male fertility in hybrids between Mus macedonicusand C57BL/6. Mammalian Genome,15, 704—10.
17. Forejt, J. (1981). Hybrid sterility gene located in the T/t — H-2supergene on chromosome 17. In Current Trends in Histocompatibility, ed. R. A. Reisfeld and S. Ferrone. New York: Plenum Press, pp 103-31.
18. Forejt, J. (1982). X-Y involvement in male sterility caused by autosome translocations: a hypothesis. In Genetic Control ofGamete Production and Function, ed. M. Fraccaro and B. Rubin. NewYork: Academic Press, pp 135-51.
19. 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.
20. Forejt, J. (1985). Chromosomal and genic sterility of hybrid type in mice and men. Experimental and Clinical Immunogenetics,2, 106-19.
21. Forejt, J. (1996). Hybrid sterility in the mouse. Trends in Genetics, 12, 412-17.
22. Forejt, J., Gregorova, 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.
23. Forejt, J. and Ivanyi, P. (1974). Genetic studies on male sterility of hybrids between laboratory and wild mice (Mus musculusL.). GeneticalResearch,24, 189-206.
24. Forejt, J., Vincek, V., Klein, J., Lehrach, H., and Loudova-Mickova, M. (1991). Genetic mapping of the t-complex region on mouse chromosome 17 including the Hybrid sterility-1gene. Mammalian Genome,1, 84-91.
25. Fossella, J., Samant, S., Silver, L., et al. (2000). An axonemal dynein at the Hybrid Sterility 6 locus: implications for thaplotype-specific male sterility and the evolution of species barriers. Mammalian Genome,11, 8-15.
26. 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, I7, 5349-63.
27. 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.
28. Good, J.M., Giger, T., Dean, M.D., and Nachman, M.W. (2010). Widespread overexpression of the X chromosome in sterile F: hybrid mice. PLoS Genetics,6, e1001148.
29. 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.
30. Gregorova, S., Divina, P., Storchova, R., et al. (2008). Mouse consomic strains: exploiting genetic divergence between Mus m. musculusand Mus m. domesticussubspecies. Genome Research,18, 509-15.
31. Gregorova, S. and Forejt, J. (2000). PWD/Ph and PWK/Ph inbred mouse strains of Mus m. musculussubspecies: a valuable resource of phenotypic variations and genomic polymorphisms. Folia Biologica (Praha), 46, 31-41.
32. Gregorova, S., Mnukova-Fajdelova, 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.
33. Grey, C., Baudat, F., and de Massy, B. (2009). Genome-wide control of the distribution of meiotic recombination. PLoS Biology,7, ei000035.
34. Guenet, J. L. (2005). The mouse genome. Genome Research,15,1729—40.
35. Guenet, J. L, Nagamine, C., Simon-Chazottes, D., Montagutelli, X., and Bonhomme, F. (1990). Hst-3: an X-linked hybrid sterility gene. GeneticalResearch,56: 163—5.
36. Haldane, J. (1922). Sex ratio and unisexual sterility in animal hybrids. Journal of Genetics, 12,101—9.
37. Handel, M. A. and Schimenti, J. C. (2010). Genetics of mammalian meiosis: regulation, dynamics and impact on fertility. Nature Reviews Genetics,11, 124—36.
38. Hayashi, K. and Matsui, Y. (2006). Meiosis-specific histone methylation is essential for meiotic progression. Tanpakushitsu Kakusan Koso,51, 441—5.
39. Hayashi, K., Yoshida, K., and Matsui, Y. (2005). A histone H3 methyltransferase controls epigenetic events required for meiotic prophase. Nature,438, 374—8.
40. Herrmann, B. G., Koschorz, B., Wertz, K., McLaughlin, K.J., and Kispert, A. (1999). A protein kinase encoded by the tcomplex responder gene causes non-Mendelian inheritance. Nature,402, 141—6.
41. Hochwagen, A. and Marais, G. A. B. (2010). Meiosis: a PRDM9 guide to the hotspots of recombination. Current Biology,20, R271—4.
42. Howell, G. R., Munroe, R. J., and Schimenti, J. C. (2005). Transgenic rescue of the mouse tcomplex haplolethal locus Thli. Mammalian Genome,16, 838—46.
43. Ivanyi, P., Vojtiskova, M., Demant, P., and Mickova, M. (1969). Genetic factors in the ninth linkage group influencing reproductive performance in male mice. Folia Biologica (Praha),15, 401—21.
44. 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.
45. Lyon, M. F. (2003). Transmission ratio distortion in mice. Annual Review of Genetics,37,393—408.
46. Macholan, M., Baird, S.J. E., Dufkova, P., et al. (2011). Assessing multilocus introgression patterns: a case study on the mouse X chromosome in Central Europe. Evolution,65,1428—46.
47. Macholan, M., Munclinger, P., Sugerkova. M., et al. (2007). Genetic analysis of autosomal and X-linked markers across a mouse hybrid zone. Evolution,61, 746—71.
48. Maheshwari, S., Wang, J., and Barbash, D.A. (2008). Recurrent positive selection of the Drosophilahybrid incompatibility gene Hmr. Molecular Biology and Evolution,25, 2421—30.
49. 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.
50. Matsuda, Y., Hirobe, T., and Chapman, V. M. (1991). Genetic basis ofX—Y chromosome dissociation and male sterility in interspecific hybrids. Proceedings ofthe National Academy of Sciences of the United States of America,88, 4850—4.
51. Mihola, O., Forejt, J., and Trachtulec, Z. (2007). Conserved alternative and antisense transcripts at the programmed cell death 2 locus. BMC Genomics,8, 20.
52. 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.
53. Muller, H.J. (1942). Isolating mechanisms, evolution, and temperature. Biological Symposia, 6, 71-125.
54. Myers, S., Bowden, R., Tumian, A., et al. (2010). Drive against hotspot motifs in primates implicates the PRDM9gene in meiotic recombination. Science,327, 876-9.
55. Neale, M.J. (2010). PRDM9 points the zinc finger at meiotic recombination hotspots. Genome Biology,11, 104.
56. 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.
57. 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.
58. 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.
59. Oliver, P. L., Goodstadt, L., Bayes, J. J., et al. (2009). Accelerated evolution of the Prdmg speciation gene across diverse metazoan taxa. PLoS Genetics,5, e1000753.
60. Paigen, K. and Petkov, P. (2010). Mammalian recombination hot spots: properties, control and evolution. Nature Reviews Genetics,11, 221-33.
61. Parvanov, E. D., Ng, S. H. S., Petkov, P.M., and Paigen, K. (2009). Trans-regulation of mouse meiotic recombination hotspots by Rcri. PLoS Biology,7, ei000036.
62. Parvanov, E. D., Petkov, P. M., and Paigen, K. (2010). Prdmgcontrols activation of mammalian recombination hotspots. Science,327, 835.
63. Phadnis, N. and Orr, H. A. (2009). A single gene causes both male sterility and segregation distortion in Drosophilahybrids. Science,323, 376-9.
64. Pialek, J., Vyskocilova, M., Bimova, B., et al. (2008). Development of unique house mouse resources suitable for evolutionary studies of speciation. Journal of Heredity, 99, 34-44.
65. 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.
66. Pilder, S. H., Olds-Clarke, P., Orth, J. M., Jester, W. F., and Dugan, L. (1997). Hstj. a male sterility mutation perturbing sperm motility, flagellar assembly, and mitochondrial sheath differentiation. Journal of Andrology,18, 663-71.
67. Pilder, S. H., Olds-Clarke, P., Phillips, D. M., and Silver, L. M. (1993). Hybrid sterility-6: amouse tcomplex locus controlling sperm flagellar assembly and movement. Developmental Biology, 159, 631-42.
68. Presgraves, D. C. (2010). Darwin and the origin of interspecific genetic incompatibilities. American Naturalist, i76(Si), S45-60.
69. 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.
70. 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.
71. Sandovici, I. And Sapienza, C. (2010). PRDM9 sticks its zinc fingers into recombination hotspots and between species. F1000 Biology Reports,2, 37.
72. She, J.X., Bonhomme, F., Boursot, P., Thaler, L., and Catzeflis, F. (1990). Molecular phylogenies in the genus Mus: comparative analysis ofelectrophoretic, scnDNA hybridization, and mtDNA RFLP data. Biological Journal of the Linnean Society,41: 83-103.
73. Storchova, R., Gregorova, S., Buckiova, D., et al. (2004). Genetic analysis ofX-linked hybrid sterility in the house mouse. Mammalian Genome,15, 515-24.
74. 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.
75. 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.
76. Thomas, J. H., Emerson, R. O., and Shendure, J. (2009). Extraordinary molecular evolution in the PRDM9 fertility gene. PLoS ONE,4, e8505.
77. 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.
78. 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. BiologicalJournal ofthe Linnean Society,84, 637-41.
79. Trachtulec, Z., Mnukova-Fajdelova, 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.
80. 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.
81. Trachtulec, Z., Vlcek, C., Mihola, O., etal. (2008). Fine haplotype structure of a chromosome 17 region in the laboratory and wild mouse. Genetics,178,1777-84.
82. Turelli, M. and Orr, H. A. (2000). Dominance, epistasis and the genetics of postzygotic isolation. Genetics,154, 1663-79.
83. Turner, J.M. A. (2007). Meiotic sex chromosome inactivation. Development,134,1823-31.
84. Vyskocilova, M., Prazanova, G., and Pialek, J. (2009). Polymorphism in hybrid male sterility in wild-derived Mus musculus musculusstrains on proximal chromosome 17. Mammalian Genome,20, 83-91.
85. Vyskocilova, M., Trachtulec, Z., Forejt, J., and Pialek, J. (2005). Does geography matter in hybrid sterility in house mice? Biological Journal of the Linnean Society,64, 663-74.