A major gene affecting age-related hearing loss in C57BL/6J mice

Hearing Research

Volumn 114, Issue 1-2, 1997, Pages 83-92

  Johnson, Kenneth R ^a   Erway, Lawrence C ^b   Cook, Susan A ^a   Willott, James F ^c   Zheng, Qing Yin ^a  

^a JACKSON LABORATORY   (United States)

^b UNIVERSITY OF CINCINNATI   (United States)

^c NORTHERN ILLINOIS UNIVERSITY   (United States)

Author keywords

Age related; Genetic mapping; Hearing loss; Mice; Non syndromic; Presbycusis

Indexed keywords

AGE RELATED HEARING LOSS; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CHROMOSOME 10; EVOKED BRAIN STEM AUDITORY RESPONSE; GENE MAPPING; GENETIC ANALYSIS; GENETIC LINKAGE; GENOTYPE; HAPLOTYPE; HEARING LOSS; MOUSE; NONHUMAN; PRESBYACUSIS; PRIORITY JOURNAL; QUANTITATIVE TRAIT;

AGING; ANIMALS; AUDITORY THRESHOLD; CHROMOSOME MAPPING; CHROMOSOMES, HUMAN, PAIR 10; COCHLEA; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; GENES, RECESSIVE; GENOTYPE; HUMANS; MICE; MICE, INBRED C57BL; PRESBYCUSIS; SPIRAL GANGLION;

EID: 0031469713     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(97)00155-X     Document Type: Article

References (41)

1. Avraham, K.B., Hasson, T., Steel, K.P., Kingsley, D.M., Russell, L.B., Mooseker, M.S., Copeland, N.G., Jenkins, N.A., 1995. The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner ear hair cells. Nat. Genet. 11, 369-375.
2. Brown, S.D., Steel, K.P., 1994. Genetic deafness - progress with mouse models. Hum. Mol. Genet. 3 (Special Issue), 1453-1456.
3. Bryda, E.C., Ling, H., Flaherty, L., 1997. A high-resolution genetic map around waltzer on mouse Chromosome 10 and identification of a new allele of waltzer. Mamm. Genome 8, 1-4.
4. Deol, M.S., 1956a. The anatomy and development of the mutants pirouette, shaker-1 and waltzer in the mouse. Proc. R. Soc. Lond. B Biol. Sci. 145, 206-213.
5. Deol, M.S., 1956b. A gene for uncomplicated deafness in the mouse. J. Embryol. Exp. Morphol. 4, 190-195.
6. Dietrich, W.F., Miller, J.C., Steen, R.G., Merchant, M., Damron, D., Nahf, R., Gross, A., Joyce, D.C., Wessel, M., Dredge, R.D., Marquis, A., Stein, L.D., Goodman, N., Page, D.C., Lander, E.S., 1994. A genetic map of the mouse with 4,006 simple sequence length polymorphisms. Nat. Genet. 7, 220-245.
7. Erway, L.C., Willott, J.F., Archer, J.R., Harrison, D.E., 1993. Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains. Hear. Res. 65, 125-132.
8. Erway, L.C., Shiau, Y.-W., Davis, R.R., Krieg, E.F., 1996. Genetics of age-related hearing loss in mice. III. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing loss. Hear. Res. 93, 181-187.
9. Gibson, F., Walsh, J., Mburu, P., Varela, A., Brown, K.A., Antonio, M., Beisel, K.W., Steel, K.P., Brown, S.D.M., 1995. A type VII myosin encoded by the mouse deafness gene shaker-1. Nature 374, 62-64.
10. Gorlin, R.J., Toriello, H.V., Cohen, M.M., 1995. in: Motulsky, A.G., Bobrow, M., Harper, P.S., Scriver, C. (Eds.), Hereditary Hearing Loss and Its Syndromes, Vol. 28. Oxford University Press, New York..
11. Guilford, P., Ayadi, H., Blanchard, S., Chaib, H., Le Paslier, D., Weissenbach, J., Drira, M., Petit, C., 1994. A human gene responsible for neurosensory, non-syndromic recessive deafness is a candidate homologue of the mouse sh-1 gene. Hum. Mol. Genet. 3, 989-993.
12. Haley, C.S., Knott, S.A., 1992. A simple regression method for mapping quantitative trait loci in line crosses using flanking markers. Heredity 69, 315-324.
13. Henry, K.R., 1983. Aging and audition. In: Willott, J.F. (Ed.), Auditory Psychobiology of the Mouse. Charles C. Thomas, Springfield, IL, pp. 470-493.
14. Henry, K.R., Chole, R.A., 1980. Genotypic differences in behavioral, physiological and anatomical expressions of age-related hearing loss on the laboratory mouse. Audiology 19, 369-383.
15. Hunter, K.P., Willott, J.F., 1987. Aging and the auditory brainstem response in mice with severe or minimal presbycusis. Hear. Res. 30, 207-218.
16. Johnson, K.R., Cook, S.A., Davisson, M.T., 1994. Identification and genetic mapping of 151 dispersed members of 16 ribosomal protein multigene families in the mouse. Mamm. Genome 5, 670-687.
17. Kelsell, D.P., Dunlop, J., Stevens, H.P., Lench, N.J., Liang, J.N., Parry, G., Mueller, R.F., Leigh, I.M., 1997. Connexin 26 mutations in hereditary non-syndromic sensorineural deafness. Nature 387, 80-83.
18. Manly, K.F., 1993. A Macintosh program for storage and analysis of experimental genetic mapping data. Mamm. Genome 4, 303-313.
19. Martinez, O., Curnow, R.N., 1992. Estimating the locations and the sizes of the effects of quantitative trait loci using flanking markers. Theor. Appl. Genet. 85, 480-488.
20. MGD, 1997. Mouse Genome Database (MGD). Mouse Genome Informatics Project, The Jackson Laboratory, Bar Harbor, ME: URL: http://www.informatics.jax.org/.
21. Mikaelian, D.O., 1979. Development and degeneration of hearing in the C57BL/6 mouse: relation of electrophysiologic responses from the round window and cochlear nucleus to cochlear anatomy and behavioral responses. Laryngoscopy 34, 1-15.
22. Morton, N.E., 1991. Genetic epidemiology of hearing loss. Ann. NY Acad. Sci. 630, 16-31.
23. Noben-Trauth, K., Zheng, Q.Y., Johnson, K.R., Nishina, P.M., 1997. mdfw: A deafness susceptibility locus that interacts with deaf waddler (dfw). Genomics 44, 266-272.
24. OMIM, 1997. Online Mendelian Inheritance in Man (OMIM). Center for Medical Genetics, Johns Hopkins University, Baltimore, MD, URL: http://www3.ncbi.nlm.nih.gov/omim/.
25. Osako, S., Hilding, D.A., 1971. Electron microscopic studies of capillary permeability in normal and Ames waltzer deaf mice. Acta Otolaryngol. 71, 365-376.
26. Parham, K., Willott, J.F., 1988. Acoustic startle response in young and aging C57BL/6 and CBA/J mice. Behav. Neurosci. 102, 881-886.
27. Schaible, R.H., 1961. Ames waltzer, av. Mouse News Lett. 24, 38.
28. Slepecky, N.B., Savage, J.E., Yoo, T.J., 1992. Localization of type II, IX, and V collagen in the inner ear. Acta Otolaryngol. 112, 611-617.
29. Southard, J.L., 1970. Jackson circler, jc. Mouse News Lett. 42, 30.
30. Steel, K.P., 1991. Similarities between mice and humans with hereditary deafness. Ann. NY Acad. Sci. 630, 68-79.
31. Steel, K.P., 1995. Inherited hearing defects in mice. Annu. Rev. Genet. 29, 675-701.
32. Steel, K.P., Brown, S.D.M., 1994. Genes and deafness. Trends Genet. 10, 428-435.
33. Weil, D., Blanchard, S., Kaplan, J., Guilford, P., Gibson, F., Walsh, J., Mburu, P., Varela, A., Levilliers, J., Weston, M.D., 1995. et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature 374, 60-61.
34. Willott, J.F., 1986. Effects of aging, hearing loss and anatomical location on thresholds of inferior colliculus neurons in C57BL/6 and CBA mice. J. Neurophysiol. 56, 391-408.
35. Willott, J.F., 1991. Aging and the Auditory System: Anatomy, Physiology and Psychophysics. Singular Press, San Diego, CA.
36. Willott, J.F., Bross, L.S., 1990. Morphology of the octopus cell area of the cochlear nucleus in young and aging C57BL/6J and CBA/J mice. J. Comp. Neurol. 300, 61-81.
37. Willott, J.F., Kulig, J., Satterfield, T., 1984. The acoustic startle response in DBA/2 and C57BL/6 mice: relationship to auditory neuronal response properties and hearing impairment. Hear. Res. 16, 161-167.
38. Willott, J.F., Jackson, L.M., Hunter, K.P., 1987. Morphometric study of the anteroventral cochlear nucleus of two mouse models of presbycusis. J. Comp. Neurol. 260, 472-480.
39. Willott, J.F., Parham, K., Hunter, K.P., 1988. Response properties of inferior colliculus neurons in middle-aged C57BL/6J mice with presbycusis. Hear. Res. 37, 15-28.
40. Willott, J.F., Erway, L.C., Archer, J.R., Harrison, D., 1995. Genetics of age-related hearing loss in mice: II. Strain differences and effects of caloric restrictions on cochlear pathology and evoked response thresholds. Hear. Res. 88, 143-155.
41. Zeng, Z.-B., 1994. Precision mapping of quantitative trait loci. Genetics 136, 1457-1468.