Assessment of hearing in 80 inbred strains of mice by ABR threshold analyses

Hearing Research

Volumn 130, Issue 1-2, 1999, Pages 94-107

  Zheng, Qing Yin ^a   Johnson, Kenneth R ^a   Erway, Lawrence C ^b  

^a JACKSON LABORATORY   (United States)

^b UNIVERSITY OF CINCINNATI   (United States)

Author keywords

Deafness model; Gene; Hearing loss; Inbred strain; Mouse; Non syndromic

Indexed keywords

ALLELISM; ANIMAL EXPERIMENT; ANIMAL MODEL; ARTICLE; AUDIOMETRY; AUDITORY SCREENING; AUDITORY THRESHOLD; BRAIN STEM RESPONSE; CONTROLLED STUDY; GENE ISOLATION; GENETIC DISORDER; HEARING; HEARING ACUITY; HEARING IMPAIRMENT; HEARING LOSS; HUMAN; INBRED STRAIN; MOUSE; NONHUMAN; PRIORITY JOURNAL; SPECIES DIFFERENCE;

ALLELES; ANIMALS; AUDITORY PATHWAYS; AUDITORY THRESHOLD; BRAIN STEM; ELECTROPHYSIOLOGY; HEARING; HEARING DISORDERS; HEARING TESTS; MICE; MICE, INBRED STRAINS; REFERENCE VALUES;

EID: 0001633148     PISSN: 03785955     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-5955(99)00003-9     Document Type: Article

References (53)

1. Atchley W.R., Fitch W. Genetic affinities of inbred mouse strains of uncertain origin. Mol. Biol. Evol. 10:1993;1150-1169.
2. Brown S.D., Steel K.P. Genetic deafness - progress with mouse models. Hum. Mol. Genet. 3:(Spec. No.):1994;1453-1546.
3. Church M.W., Shucard D.W. Age-related hearing loss in BDF1 mice as evidenced by the brainstem auditory evoked potential. Audiology. 25:1986;363-372.
4. Deol M.S. A gene for uncomplicated deafness in the mouse. J. Embryol. Exp. Morphol. 4:1956;190-195.
5. Ehret, G., 1983. Psychoacoustics. In: Willot, J.F. (Ed.), Auditory Psychobiology of the Mouse. Charles C. Thomas, Springfield, IL, pp. 13-53.
6. Erkman L., McEvilly R.J., Luo L., Ryan A.K., Hooshmand F., O'Connell S.M., Keithley E.M., Rapaport D.H., Ryan A.F., Rosenfeld M.G. Role of transcription factors Brn-3.1 and Brn-3.2 in auditory and visual system development. Nature. 381:1996;603-606.
7. Erway L.C., Willott J.F., Archer J.R., Harrison D.E. Genetics of age-related hearing loss in mice: I. Inbred and F1 hybrid strains. Hear. Res. 65:1993;125-132.
8. Erway L.C., Shiau Y.W., Davis R.R., Krieg E.F. Genetics of age-related hearing loss in mice. III. Susceptibility of inbred and F1 hybrid strains to noise-induced hearing loss. Hear. Res. 93:1996;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. A type VII myosin encoded by the mouse deafness gene shaker-1. Nature. 374:1995;62-64.
10. Hall J.W. 3rd., Rupp K.A. Auditory brainstem response: recent developments in recording and analysis. Adv. Otorhinolaryngol. 53:1997;21-45.
11. Henry K.R. Age-related auditory loss and genetics: an electrocochleographic comparison of six inbred strains of mice. J. Gerontol. 37:1982;275-282.
12. Henry K.R., McGinn M.D. The mouse as a model for human audition. A review of the literature. Audiology. 31:1992;181-189.
13. Henry K.R., McGinn M.D., Carter L.A., Savoska E.A. Auditory brainstem function of the F1 offspring of the cross of CBA/CaJ and AU/SsJ inbred mice. Audiology. 31:1992;190-195.
14. Hunter K.P., Willott J.F. Aging and the auditory brainstem response in mice with severe of minimal presbycusis. Hear. Res. 30:1987;207-218.
15. Johnson K.R., Erway L.C., Cook S.A., Willott J.F., Zheng Q.Y. A major gene affecting age-related hearing loss in C57BL/6J mice. Hear. Res. 114:1997;83-92.
16. Johnstone J.R., Alder V.A., Johnstone B.M., Robertson D., Yates G.K. Cochlear action potential threshold and single unit thresholds. J. Acoust. Soc. Am. 65:1979;254-257.
17. Keats B.J., Nouri N., Huang J.M., Money M., Webster D.B., Berlin C.I. The deafness locus (dn) maps to mouse chromosome 19. Mamm. Genome. 6:1995;8-10.
18. Kikutani H., Makino S. The murine autoimmune diabetes model: NOD and related strains. Adv. Immunol. 51:1992;285-322.
19. Kim D.O., Paparello J., Jung M.D., Smurzynski J., Sun X. Distortion product otoacoustic emission test of sensorineural hearing loss: performance regarding sensitivity, specificity and receiver operating characteristics. Acta Otolaryngol. (Stockh.). 116:1996;3-11.
20. Leiter, E.H., 1998. NOD mice and related strains: origin, husbandry, and biology. In: Leiter, E.H., Atkinson, M.A. (Eds.), NOD Mice and Related Strains: Research Applications in Diabetes, AIDS, Cancer, and Other Disease. Landes, Austin, TX, pp. 1-35.
21. Liu X.Z., Walsh J., Mburu P., Kendrick-Jones J., Cope M.J., Steel K.P., Brown S.D. Mutations in the myosin VIIA gene cause non-syndromic recessive deafness. Nature Genet. 16:1997;188-190.
22. Liu X.Z., Walsh J., Tamagawa Y., Kitamura K., Nishizawa M., Steel K.P., Brown S.D. Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene (letter). Nature Genet. 17:1997;268-269.
23. Lyon, M.F., Rastan, S., Brown, S.D.M., 1996. Genetic Variants and Strains of the Laboratory Mouse. Oxford University Press, Oxford.
24. Markand O.N. Brainstem auditory evoked potentials. J. Clin. Neurophysiol. 11:1994;319-342.
25. Martini A., Milani M., Rosignoli M., Mazzoli M., Prosser S. Audiometric patterns of genetic non-syndromal sensorineural hearing loss. Audiology. 36:1997;228-236.
26. McFadden S.L., Willott J.F. Responses of inferior colliculus neurons in C57BL/6J mice with and without sensorineural hearing loss: effects of changing the azimuthal location of an unmasked pure-tone stimulus. Hear. Res. 78:1994;115-131.
27. Møller A.R. Auditory neurophysiology. J. Clin. Neurophysiol. 11:1994;284-308.
28. Morton N.E. Genetic epidemiology of hearing impairment. Ann. NY Acad. Sci. 630:1991;16-31.
29. Noben-Trauth K., Zheng Q.Y., Johnson K.R., Nishina P.M. mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw). Genomics. 44:1997;266-272.
30. Parham K. Distortion product otoacoustic emissions in the C57BL/6J mouse model of age-related hearing loss. Hear. Res. 112:1997;216-234.
31. Petit C. Genes responsible for human hereditary deafness: symphony of a thousand. Nature Genet. 14:1996;385-391.
32. Pieke-Dahl S., Ohlemiller K.K., McGee J., Walsh E.J., Kimberling W.J. Hearing loss in the RBF/DnJ mouse, a proposed animal model of Usher syndrome type IIa. Hear. Res. 112:1997;1-12.
33. Probst F.J., Fridell R.A., Raphael Y., Saunders T.L., Wang A., Liang Y., Morell R.J., Touchman J.W., Lyons R.H., Noben-Trauth K., Friedman T.B., Camper S.A. Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene (see comments). Science. 280:1998;1444-1447.
34. Prochazka M., Serreze D.V., Frankel W.N., Leiter E.H. NOR/Lt mice: MHC-matched diabetes-resistant control strain for NOD mice. Diabetes. 41:1992;98-106.
35. Sekiguchi F., Ishibashi K., Katoh H., Kawamoto Y., Ino T. Genetic profile of alloxan-induced diabetes-susceptible mice (ALS) and -resistant mice (ALR). Jikken Dobutsu. 39:1990;269-272.
36. Shone G., Altschuler R.A., Miller J.M., Nutall A.L. The effect of noise exposure on the aging ear. Hear. Res. 56:1991;173-178.
37. Simpson E.M., Linder C.C., Sargent E.E., Davisson M.T., Mobraaten L.E., Sharp J.J. Genetic variation among 129 substrains and its importance for targeted mutagenesis in mice. Nature Genet. 16:1997;19-27.
38. Smith S.M., Forbes P.D., Linna T.J. Immune responses in nonhaired mice. Int. Arch. Allergy Appl. Immunol. 67:1982;254-261.
39. Steel K.P. Inherited hearing defects in mice. Annu. Rev. Genet. 29:1995;675-701.
40. Steel K.P., Bock G.R. Hereditary inner-ear abnormalities in animals. Relationships with human abnormalities. Arch. Otolaryngol. 109:1983;22-29.
41. Steel K.P., Brown S.D. Genetics of deafness. Curr. Opin. Neurobiol. 6:1996;520-525.
42. Steel K.P., Moorjani P., Bock G.R. Mixed conductive and sensorineural hearing loss in LP/J mice. Hear. Res. 28:1987;227-236.
43. Stockard J.J., Rossiter V.S., Jones T.A., Sharbrough F.W. The effects of centrally acting drug on brainstem auditory responses. Electroencephalogr. Clin. Neurophysiol. 43:1977;550-551.
44. Sun X.M., Jung M.D., Kim D.O., Randolph K.J. Distortion product otoacoustic emission test of sensorineural hearing loss in humans: comparison of unequal- and equal-level stimuli. Ann. Otol. Rhinol. Laryngol. 105:1996;982-990.
45. Taketo M., Schroeder A.C., Mobraaten L.E., Gunning K.B., Hanten G., Fox R.R., Roderick T.H., Stewart C.L., Lilly F., Hansen C.T., et al. FVB/N: an inbred mouse strain preferable for transgenic analyses. Proc. Natl. Acad. Sci. USA. 88:1991;2065-2069.
46. Vahava O., Morell R., Lynch E.D., Weiss S., Kagan M.E., Ahituv N., Morrow J.E., Lee M.K., Skvorak A.B., Morton C.C., Blumenfeld A., Frydman M., Friedman T.B., King M.C., Avraham K.B. Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans. Science. 279:1998;1950-1954.
47. Van Camp, G., Smith, R.J., 1998. Hereditary Hearing Loss Homepage. World Wide Web URL: http://dnalab-www.uia.ac.be/dnalab/hhh/.
48. Walton J.P., Frisina R.D., Meierhans L.R. Sensorineural hearing loss alters recovery from short-term adaptation in the C57BL/6 mouse. Hear. Res. 88:1995;19-26.
49. Wang A., Liang Y., Fridell R.A., Probst F.J., Wilcox E.R., Touchman J.W., Morton C.C., Morell R.J., Noben-Trauth K., Camper S.A., Friedman T.B. Association of unconventional myosin MYO15 mutations with human nonsyndromic deafness DFNB3 (see comments). Science. 280:1998;1447-1451.
50. Weil D., Blanchard S., Kaplan J., Guilford P., Gibson F., Walsh J., Mburu P., Varela A., Levilliers J., Weston M.D., et al. Defective myosin VIIA gene responsible for Usher syndrome type 1B. Nature. 374:1995;60-61.
51. nod strains. In: Act, F.W., Vogel, H.J. (Eds.), Molecular Mechanisms of Immunological Self-Recognition. Academic Press, San Diego, CA, pp. 173-181.
52. Willott, J.F., 1983. Auditory Psychobiology of the Mouse. Charles C. Thomas, Springfield, IL.
53. Willott J.F., Erway L.C., Archer J.R., Harrison D.E. Genetics of age-related hearing loss in mice. II. Strain differences and effects of caloric restriction on cochlear pathology and evoked response thresholds. Hear. Res. 88:1995;143-155.