Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1991 Jun 15;88(12):5408–5412. doi: 10.1073/pnas.88.12.5408

Genetic dissection of susceptibility to audiogenic seizures in inbred mice.

P E Neumann 1, R L Collins 1
PMCID: PMC51882  PMID: 2052619

Abstract

Mice of some inbred strains, such as 21-day-old DBA/2J mice, have generalized convulsions when exposed to intense auditory stimulation. Analysis of susceptibility to audiogenic seizures in BXD recombinant inbred strains has demonstrated the influence of at least three loci. One locus, Asp-1, is located on chromosome 12 between Ah and D12Nyu1; another locus, Asp-2, is on chromosome 4, tightly linked to b. Here we report evidence that Asp-2 is located within an 8-centimorgan segment distal to b and that Asp-3 is linked to Mtv-1 on chromosome 7. We also present evidence that these three loci account for most of the heritable variation in susceptibility to audiogenic seizures in crosses of DBA/2J and C57BL/6J mice and that susceptibility to audiogenic seizures is influenced by genomic imprinting. Thus, genomic imprinting may complicate linkage and mapping studies and should be considered in analyses of complex modes of inheritance.

Full text

PDF
5408

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Collins R. L. A new genetic locus mapped from behavioral variation in mice: audiogenic seizure prone (ASP). Behav Genet. 1970 May;1(2):99–109. doi: 10.1007/BF01071825. [DOI] [PubMed] [Google Scholar]
  2. Collins R. L., Fuller J. L. Audiogenic seizure prone (asp): a gene affecting behavior in linkage group 8 of the mouse. Science. 1968 Dec 6;162(3858):1137–1139. doi: 10.1126/science.162.3858.1137. [DOI] [PubMed] [Google Scholar]
  3. De Maeyer E., Dandoy F. Linkage analysis of the murine interferon alpha locus (Ifa) on chromosome 4. J Hered. 1987 May-Jun;78(3):143–146. doi: 10.1093/oxfordjournals.jhered.a110346. [DOI] [PubMed] [Google Scholar]
  4. FULLER J. L., EASLER C., SMITH M. E. Inheritance of audiogenic seizure susceptibility in the mouse. Genetics. 1950 Nov;35(6):622–632. doi: 10.1093/genetics/35.6.622. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Frankel W. N., Stoye J. P., Taylor B. A., Coffin J. M. Genetic analysis of endogenous xenotropic murine leukemia viruses: association with two common mouse mutations and the viral restriction locus Fv-1. J Virol. 1989 Apr;63(4):1763–1774. doi: 10.1128/jvi.63.4.1763-1774.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Fuller J. L., Sjursen F. H., Jr Audiogenic seizures in eleven mouse strains. J Hered. 1967 May-Jun;58(3):135–140. doi: 10.1093/oxfordjournals.jhered.a107565. [DOI] [PubMed] [Google Scholar]
  7. Hall J. G. Genomic imprinting: review and relevance to human diseases. Am J Hum Genet. 1990 May;46(5):857–873. [PMC free article] [PubMed] [Google Scholar]
  8. Henry K. R. Audiogenic seizure susceptibility induced in C57BL-6J mice by prior auditory exposure. Science. 1967 Nov 17;158(3803):938–940. doi: 10.1126/science.158.3803.938-a. [DOI] [PubMed] [Google Scholar]
  9. Knoll J. H., Nicholls R. D., Magenis R. E., Graham J. M., Jr, Lalande M., Latt S. A. Angelman and Prader-Willi syndromes share a common chromosome 15 deletion but differ in parental origin of the deletion. Am J Med Genet. 1989 Feb;32(2):285–290. doi: 10.1002/ajmg.1320320235. [DOI] [PubMed] [Google Scholar]
  10. Monk M. Genomic imprinting. Genes Dev. 1988 Aug;2(8):921–925. doi: 10.1101/gad.2.8.921. [DOI] [PubMed] [Google Scholar]
  11. Monk M. Variation in epigenetic inheritance. Trends Genet. 1990 Apr;6(4):110–114. doi: 10.1016/0168-9525(90)90124-o. [DOI] [PubMed] [Google Scholar]
  12. Nadeau J. H., Berger F. G., Kelley K. A., Pitha P. M., Sidman C. L., Worrall N. Rearrangement of genes located on homologous chromosomal segments in mouse and man: the location of genes for alpha- and beta-interferon, alpha-1 acid glycoprotein-1 and -2, and aminolevulinate dehydratase on mouse chromosome 4. Genetics. 1986 Dec;114(4):1239–1255. doi: 10.1093/genetics/114.4.1239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Neumann P. E., Seyfried T. N. Mapping of two genes that influence susceptibility to audiogenic seizures in crosses of C57BL/6J and DBA/2J mice. Behav Genet. 1990 Mar;20(2):307–323. doi: 10.1007/BF01067798. [DOI] [PubMed] [Google Scholar]
  14. Neumann P. E. Two-locus linkage analysis using recombinant inbred strains and Bayes' theorem. Genetics. 1990 Sep;126(1):277–284. doi: 10.1093/genetics/126.1.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Nicholls R. D., Knoll J. H., Butler M. G., Karam S., Lalande M. Genetic imprinting suggested by maternal heterodisomy in nondeletion Prader-Willi syndrome. Nature. 1989 Nov 16;342(6247):281–285. doi: 10.1038/342281a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. Ottman R., Annegers J. F., Hauser W. A., Kurland L. T. Higher risk of seizures in offspring of mothers than of fathers with epilepsy. Am J Hum Genet. 1988 Sep;43(3):257–264. [PMC free article] [PubMed] [Google Scholar]
  17. Palayoor S. T., Seyfried T. N. Genetic association between Ca2+-ATPase activity and audiogenic seizures in mice. J Neurochem. 1984 Jun;42(6):1771–1774. doi: 10.1111/j.1471-4159.1984.tb12771.x. [DOI] [PubMed] [Google Scholar]
  18. Racine R. R., Langley C. H. Genetic analysis of protein variations in Mus musculus using two-dimensional electrophoresis. Biochem Genet. 1980 Feb;18(1-2):185–197. doi: 10.1007/BF00504368. [DOI] [PubMed] [Google Scholar]
  19. Schlesinger K., Elston R. C., Boggan W. The genetics of sound induced seizure in inbred mice. Genetics. 1966 Jul;54(1):95–103. doi: 10.1093/genetics/54.1.95. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Seyfried T. N. Genetic heterogeneity for the development of audiogenic seizures in mice. Brain Res. 1983 Jul 25;271(2):325–329. doi: 10.1016/0006-8993(83)90294-9. [DOI] [PubMed] [Google Scholar]
  21. Seyfried T. N., Glaser G. H. Genetic linkage between the AH locus and a major gene that inhibits susceptibility to audiogenic seizures in mice. Genetics. 1981 Sep;99(1):117–126. doi: 10.1093/genetics/99.1.117. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Seyfried T. N., Glaser G. H., Yu R. K., Palayoor S. T. Inherited convulsive disorders in mice. Adv Neurol. 1986;44:115–133. [PubMed] [Google Scholar]
  23. Seyfried T. N., Yu R. K., Glaser G. H. Genetic analysis of audiogenic seizure susceptibility in C57BL/6J X DBA/2J recombinant inbred strains of mice. Genetics. 1980 Mar;94(3):701–718. doi: 10.1093/genetics/94.3.701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Shire J. G. Unequal parental contributions: genomic imprinting in mammals. New Biol. 1989 Nov;1(2):115–120. [PubMed] [Google Scholar]
  25. Solter D. Differential imprinting and expression of maternal and paternal genomes. Annu Rev Genet. 1988;22:127–146. doi: 10.1146/annurev.ge.22.120188.001015. [DOI] [PubMed] [Google Scholar]
  26. Traina V. L., Taylor B. A., Cohen J. C. Genetic mapping of endogenous mouse mammary tumor viruses: locus characterization, segregation, and chromosomal distribution. J Virol. 1981 Dec;40(3):735–744. doi: 10.1128/jvi.40.3.735-744.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES