Hostname: page-component-848d4c4894-x24gv Total loading time: 0 Render date: 2024-05-10T22:05:39.959Z Has data issue: false hasContentIssue false
  • English
  • Français

Y-chromosomal DNA polymorphism in mouse inbred strains

Published online by Cambridge University Press:  14 April 2009

Yutaka Nishioka
Yutaka Nishioka
Affiliation:
Department of Biology, McGill University, Montreal, Quebec, Canada H3A 1B1
Rights & Permissions [Opens in a new window]

Summary

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Mice are the most widely used experimental mammals, and many inbred strains are available. However, except for the relatively recent strains derived from known wild populations, the relationships between wild and laboratory mice are not well understood. Based on the Y-chromosomal restriction fragmentlength polymorphism, seventeen inbred strains were classified into two groups: strains with the Mus musculus musculus type Y chromosome and those with the M. m. domesticus type Y chromosome. We extended the survey to an additional twenty-two inbred strains. The M. m. musculus type Y chromosome was found in AEJ/GnLe, AAU/SsJ, BDP/J, BXSB/MpJ, DA/HuSn, HTG/GoSfSn, I/LnJ, LP/J, NZW/LacJ, RIIIS/J, SB/Le, SEA/GnJ, SF/CamEi, SK/CamEi, SM/J, WB/ReJ, WC/ReJ and YBR/Ei, while the M. m. domesticus type Y chromosome was present in BUB/BnJ, MA/MyJ, PL/J and ST/bJ.

Type
Research Article
Information
Genetics Research , Volume 50 , Issue 1 , August 1987 , pp. 69 - 72
Copyright
Copyright © Cambridge University Press 1987

References

Bishop, C. E., Boursot, P., Baron, B., Bonhomme, F. & Hatat, D. (1985). Most classical Mus musculus domesticus laboratory mouse strains carry a Mus musculus musculus Y chromosome. Nature 315, 70–72.CrossRefGoogle ScholarPubMed
Denhardt, D. T. (1966). A membrane-filter technique for the detection of complementary DNA. Biochemical and Biophysical Research Communications 23, 641–646.CrossRefGoogle ScholarPubMed
Ferris, S. D., Sage, R. D., Prager, E. M., Ritte, U. & Wilson, A. C. (1983). Mitochondrial DNA evolution in mice. Genetics 105, 681–721.CrossRefGoogle ScholarPubMed
Ferris, S. D., Sage, R. D. & Wilson, A. C. (1982). Evidence from mtDNA sequence that common laboratory strains of inbred mice are descended from a single female. Nature 295, 163–165.CrossRefGoogle ScholarPubMed
Festing, M. F. W. & Lovell, D. P. (1981). Domestication and development of the mouse as a laboratory animal. Symposia of the Zoological Society of London 47, 43–62.Google Scholar
Hunt, W. G. & Selander, R. K. (1973). Biochemical genetics of hybridization in European house mice. Heredity 31, 11–33.CrossRefGoogle ScholarPubMed
Keeler, C. D. (1931). The Laboratory Mouse: its Origin, Heredity and Culture. Cambridge, Mass.: Harvard University Press.CrossRefGoogle Scholar
Lamar, E. E. & Palmer, E. (1984). Y-encoded, species- specific DNA in mice: evidence that the Y chromosome exists in two polymorphic forms in inbred strains. Cell 37, 171–177.CrossRefGoogle Scholar
Marshall, J. T. (1981). Taxonomy. In The Mouse in Biomedical Research, (edited by Berry, R. J.) vol. 1, pp. 17–26. New York: Academic Press.Google Scholar
Morse, H. C. III (1978). Introduction. In Origins of Inbred Mice, pp. 3–21. New York: Academic Press.CrossRefGoogle Scholar
Nishioka, Y. & Lamothe, E. (1986). Isolation and characterization of a mouse Y chromosomal repetitive sequence. Genetics 113, 417–432.CrossRefGoogle ScholarPubMed
Potter, M. (1978). Comments on the relationship of inbred strains to the genus Mus. In Origins of Inbred Mice, (edited by Morse, H. C. III) pp. 497–509. New York: Academic Press.CrossRefGoogle Scholar
Rice, M. C. & O'Brien, S. J. O. (1980). Genetic variance of laboratory outbred Swiss mice. Nature 283, 157–161.CrossRefGoogle ScholarPubMed
Sage, R. D. (1981). Wild mice. In The Mouse in Biomedical Research, (edited by Berry, R. J.) vol. 1, pp. 39–90. New York: Academic Press.Google Scholar
Selander, R. K., Hunt, W. G. & Yang, S. Y. (1969). Protein polymorphism and genetic heterozygosity in two European subspecies of house mouse. Evolution 23, 379–390.CrossRefGoogle Scholar
Southern, E. M. (1975). Detection of specific sequence among DNA fragments separated by gel electrophoresis. Journal of Molecular Biology 98, 503–517.CrossRefGoogle Scholar
Staats, J. (1980). Standardized nomenclature for inbred strains of mice: seventh listing. Cancer Research 40, 2083–2128.Google ScholarPubMed
Thaler, L., Bonhomme, F. & Britton-Davidian, J. (1981). Process of speciation and semispeciation in the house mouse. Symposia of the Zoological Society of London 47, 27–41.Google Scholar
Yonekawa, H., Gotoh, O., Tagashira, Y., Shi, L.-L, Cho, W. S., Miyashita, N. & Moriwaki, K. (1986). A hybrid origin of Japanese mice Mus musculus molossinus. Current Topics in Microbiology and Immunology 127, 62–67.Google ScholarPubMed
Yonekawa, H., Moriwaki, K., Gotoh, O., Miyashita, N., Migita, S., Bonhomme, F., Hjorth, J. P., Petras, M. L. & Tagashira, Y. (1982). Origins of laboratory mice deduced from restriction patterns of mitochondrial DNA. Differentiation 22, 222–226.CrossRefGoogle ScholarPubMed
Yonekawa, H., Moriwaki, K., Gotoh, O., Watanabe, J., Hayashi, J.-I., Miyashita, N., Petras, M. L. & Tagashira, Y. (1980). Relationship between laboratory mice and the subspecies Mus musculus domesticus based on restriction endonuclease cleavage patterns of mitochondrial DNA. Japanese Journal of Genetics 55, 289–296.Google Scholar