Full-text resources of PSJD and other databases are now available in the new Library of Science.
Visit https://bibliotekanauki.pl

PL EN


Preferences help
enabled [disable] Abstract
Number of results

Journal

2006 | 55 | 1 | 107-116

Article title

Specjacja u myszy domowych, mus musculus - mechanizmy izolujące

Content

Title variants

EN
Speciation in the house mouse, mus musculus - mechanisms of isolation

Languages of publication

PL EN

Abstracts

EN
Speciation, the formation of species, is a central problem in evolutionary biology. The genetic basis and evolution of reproductive isolation between taxa is a key for understanding speciation. The house mouse Mus musculus is an excellent model for the study of reproductive isolation. Two subspecies, M. m. musculus and M. m. domesticus that diverged from each other approximately between 1,000,000-350,000 years ago, form a narrow hybrid zone that extends across Europe. The standard chromosome complement of this species consists of 40 acrocentric chromosomes. However, in M. m. domesticus there are many local karyotypic races that are characterised by different sets of acrocentrics and metacentrics. Accumulation of chromosomal rearrangements may lead to reproductive isolation between populations. The first theoretical model of this process was postulated by Dobzhansky (1937) and Muller (1942). They expressed the idea that speciation is a by-product of independent divergence between populations. The hybrid zone between sister mouse taxa can be used to identify genomic regions underlying reproductive isolation. Variation in the degree of gene flow across the hybrid zone is measured using molecular markers. Thus, mice offer a unique opportunity to study relationships between genotype and phenotype.

Keywords

Journal

Year

Volume

55

Issue

1

Pages

107-116

Physical description

Dates

published
2006

Contributors

  • Zakład Badania Ssaków Polskiej Akademii Nauk, Waszkiewicza 1c, 17-230 Białowieża, Polska
  • Zakład Badania Ssaków Polskiej Akademii Nauk, Waszkiewicza 1c, 17-230 Białowieża, Polska

References

  • Boursot P., Auffray J. C., Britton-Davidian J., Bonhomme F., 1993. The evolution of house mice. Ann. Rev. Ecol. Syst. 24, 119-152.
  • Božíková E., Munclinger P., Teeter K., Tucker P., Macholán M., Piálek J., 2005. Mitochondrial DNA in the hybrid zone between Mus musculus musculus and Mus musculus domesticus: a comparison of two transects. Biol. J. Linn. Soc. 84, 363-378.
  • Britton-Davidian J., Catalan J., Ramalhinho M. G.., Ganem G., Auffray J. C., Capela R., Biscoito M., Searle J. B., da Luz Mathias M., 2000. Rapid chromosomal evolution in island mice. Nature 403, 158.
  • Coyne J. A., Orr H. A., 1989. Patterns of speciation in Drosophila. Evolution 43, 362-381.
  • Coyne J. A., Orr H. A., 1997. ''Patterns of speciation in Drosophila'' revisited. Evolution 51, 295-303.
  • Coyne J. A., Orr H. A., 1998. The evolutionary genetics of speciation. Phil. Trans. R. Soc. Lond. B 353, 287-305.
  • Dietrich W. F., Miller J., Steen R., Merchant M. A., Damron-Boles D., Husain Z., Dredge R., Daly M. J., Ingalls K. A., O'Connor T. J., Evans C. A., DeAngelis M. M., Levinson D. M., Kruglyak L., Goodman N., Copeland N. G., Jenkins N. A., Hawkins T. L., Stein L., Page D. C., Lander E. S., 1996. A comprehensive genetic map of the mouse genome. Nature 380, 149-152.
  • Dobzhansky T., 1937. Genetics and the Origin of Species. Columbia University Press, New York.
  • Dod B., Jermiin L. S., Boursot P., Chapman V. H., Nielsen J. T., Bonhomme F., 1993. Counterselection on sex chromosomes in the Mus musculus European hybrid zone. J. Evol. Biol. 6, 529-546.
  • Elliott R. W., Miller D. R., Pearsall R. S., Hohman C., Zhang Y. K., Poslinski D., Tabaczynski D. A., Chapman V. M., 2001. Genetic analysis of testis weight and fertility in an interspecies hybrid congenic strain for chromosome X. Mamm. Genome 12, 45-51.
  • Forejt J., 1996. Hybrid sterility in the mouse. Trends in Genetics 12, 412-417.
  • Forejt J., Iványi P., 1975. Genetic studies on male sterility of hybrids between laboratory and wild mice (Mus musculus L.). Genet. Res. 24, 189-206.
  • Gropp A., Tettenborn U., von Lehmann E., 1969. Chromosomenuntersuchungen bei der Tabakmaus (M. poschiavinus) und bei den Hybriden mit der Laboratorumsmaus. Experientia 25, 875-876.
  • Haldane J. B. S., 1922. Sex-ratio and unisexual sterility in hybrid animals. J. Genetics 12, 101-109.
  • Hayashi T. I., Kawata M., 2002. How genes causing unfit hybrids evolve within populations: a review of models of postzygotic isolation. Popul. Ecol. 44, 157-163.
  • Howard D. J., Marshall J. L., Hampton D. D., Britch S. C., Draney M. L., Chu J., Cantrell R. G., 2002. The genetics of reproductive isolation: A retrospective and prospective look with comments on ground crickets. Am. Nat. 159 (Suppl.), S8-S21.
  • Inoue N., Ikawa M., Isotani A., Okabe M., 2005. The immunoglobulin superfamily protein Izumo is required for sperm to fuse with eggs. Nature 434, 234-238.
  • Johnson N. A., 2000. Speciation: Dobzhansky-Muller incompatibilities, dominance and gene interactions. TREE 15, 480-482.
  • Juneja R., Agulnik S. I., Silver L. M., 1998. Sequence divergence within the sperm-specific polypeptide TCTE1 is correlated with species-specific differences in sperm binding to zona-intact eggs. J. Andrology 19, 183-188.
  • Macholán M., Kryštufek B., Vohralík V., 2003. The location of the Mus musculus/M. domesticus hybrid zone in the Balkans: Clues from morphology. Acta Theriol. 48, 177-188.
  • Mallet J., 2005. Hybridization as an invasion of the genome. TREE 20, 229-237.
  • Mouse Genome Sequencing Consortium, 2002. Initial sequencing and comparative analysis of the mouse genome. Nature 420, 520-562.
  • Muller H. J., 1940. Bearing of the 'Drosophila' work on systematics. [W:] The new systematics. Huxley J. (red.). Oxford University Press, London, 185-268.
  • Muller H. J., 1942. Isolating mechanisms, evolution and temperature. Biol. Symp. 6, 71-125.
  • Musser G. G., Carleton M. D., 2005. Superfamily Muroidea. [W:] Mammal species of the world: a taxonomic and geographic reference. Wydanie 3. Wilson D. E., Reeder D. A. (red.). The Johns Hopkins University Press, Baltimore, 894-1531.
  • Nachman M. W., Searle J. B., 1995. Why is the house mouse karyotype so variable? TREE 10, 397-402.
  • Oka A, Mita A., Sakurai-Yamatani N., Yamamoto H., Takagi N., Takano-Shimizu T., Toshimori K., Moriwaki K., Shiroishi T., 2004. Hybrid breakdown caused by substitution of the X chromosome between two mouse subspecies. Genetics 166, 913-924.
  • Orth A., Belkhir K., Britton-Davidian J., Boursot P., Benazzou T., Bonhomme F., 2002. Natural hybridisation between two sympatric species of mice Mus musculus domesticus L. and Mus spretus Lataste. C. R. Biologies 325, 89-97.
  • Payseur B. A., Nachman M. W., 2005. The genomics of speciation: investigating the molecular correlates of X chromosome introgression across the hybrid zone between Mus domesticus and Mus musculus. Biol. J. Linn. Soc. 84, 523-534.
  • Payseur B. A., Krenz J. G., Nachman M. W., 2004. Differential patterns of introgression across the X chromosome in a hybrid zone between two species of house mice. Evolution 58, 2064-2078.
  • Piálek J., Hauffe H. C., Rodriguez-Clark K. M., Searle J. B., 2001. Raciation and speciation in house mice from the Alps: the role of chromosomes. Mol. Ecol. 10, 613-625.
  • Piálek J., Hauffe H. C., Searle J. B., 2005. Chromosomal variation in the house mouse. Biol. J. Linn. Soc. 84, 535-563.
  • Pilder S. H., 1997. Identification and linkage mapping of Hst7, a new M. spretus/M. m. domesticus chromosome 17 hybrid sterility locus. Mamm. Genome 8, 290-291.
  • Pletcher M. T., McClurg P., Batalov S., Su A. I., Barnes S. W., Lagler E., Korstanje R. Wang X., Nusskern D., Bogue M. A., Mural R. J., Paigen B., Wiltshire T., 2004. Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse. PLoS Biology 2, 2159-2169.
  • Presgraves D. C., 2003. A fine-scale genetic analysis of hybrid incompatibilities in Drosophila. Genetics 163, 955-972.
  • Rieseberg L.H., 2001. Chromosomal rearrangements and speciation. TREE 16, 351-358.
  • Sage R. D., Atchley W. R., Capanna E., 1993. House mice as models in systematic biology. Syst. Biol. 42, 523-561.
  • Saetre G. P., Borge T., Lindroos K., Haavie J., Sheldon B. C., Primmer C., Syvanen A. C., 2003. Sex chromosome evolution and speciation in Ficedula flycatchers. Proc. R. Soc. London B 270, 53-59.
  • Searle J. B., 1998. Speciation, Chromosomes, and Genomes. Genome Research 8, 1-3.
  • Searle J. B., Wójcik J. M., 1998. Chromosomal evolution: the case of Sorex araneus. [W:] Evolution of Shrews. Wójcik J. M., Wolsan M. (red.). Mammal Research Institute, Białowieża, 219-268.
  • She J., Bonhomme F., Boursot P., Thaler L., Catzeflis F., 1990. Molecular phylogenies in the genus Mus: Comparative analysis of electrophoretic, scnDNA hybridization, and mtDNA RFLP data. Biol. J. Linn. Soc. Lond. 41, 83-103.
  • Silver L. M., 1995. Mouse Genetics. Concepts and Applications. Oxford University Press, New York:
  • Storchová R., Gregorová S., Buckiová D., Kyselová V., Divina P., Forejt J., 2004. Genetic analysis of X-linked hybrid sterility in the house mouse. Mamm. Genome 15, 515-524.
  • Swanson W. J., Vacquier V. D., 2002. Reproductive protein evolution. Ann. Rev. Ecol. Syst. 33, 161-179.
  • Tao Y., Chen S., Hartl D. L., Laurie C. C., 2003. Genetic dissection of hybrid incompatibilities between Drosophila simulans and D. mauritiana. I. Differential accumulation of hybrid male sterility effects on the X and autosomes. Genetics 164, 1383-1397.
  • True J. R., Weir B. S., Laurie C. C., 1996. A genome-wide survey of hybrid incompatibility factors by the introgression of marked segments of Drosophila mauritiana chromosomes into Drosophila simulans. Genetics 142, 819-837.
  • Tucker P. K., Sage R. D., Warner J., Wilson A. C., Eicher E. M., 1992. Abrupt cline for sex chromosomes in a hybrid zone between two species of mice. Evolution 46, 1146-1163.
  • Turelli M., Barton N. H., Coyne J. A., 2001. Theory and speciation. TREE 16, 330-342.
  • Vyskočilová M., Trachtulec Z., Forejt J., Piálek J., 2005. Does geography matter in the hybrid sterility in house mice? Biol. J. Linn. Soc. 84, 663-674.
  • Wade C. M., Kulbokas E. J., Kirby A. W., Zody M. C., Mullikin J. C., Lander E. S., Lindblad-Toh K., Daly M. J., 2002. The mosaic structure of variation in the laboratory mouse genome. Nature 420, 574-578.
  • Wójcik A. M., 1982. Problemy systematyki myszy domowej. Przegl. Zool. 26, 459-464.
  • Wu C.-I., 2001. The genic view of the process of speciation. J. Evol. Biol. 14, 851-865.
  • Wu C.-I., Davis A. W., 1993. Evolution of postmating reproductive isolation: the composite nature of Haldane's rule and its genetic bases. Am. Nat. 142, 187-212.
  • Wu C.-I., Hollocher H., 1998. Subtle is nature. The genetics of species differentiation and speciation. [W:] Endless Forms. Species and speciation. Howard D. J., Berlocher S. H. (red.). Oxford University Press, Oxford, 339-351
  • Wu C.-I., Johnson N. A., Palopoli M. F., 1996. Haldane's rule and its legacy: why are there so many sterile males? TREE 11, 281-284.
  • Zima J., Gaichenko V. A., Macholán M., Radjabli S. I., Sablina O. V., Wójcik J. M., 1990. Are Robertsonian variations a frequent phenomenon in mouse populations in Eurasia? Biol. J. Linn. Soc. Lond. 41, 229-233.

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.bwnjournal-article-ksv55p107kz
JavaScript is turned off in your web browser. Turn it on to take full advantage of this site, then refresh the page.