| Autor: |
Griffith AJ; Hearing Section, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Rockville, MD 20850, USA., Szymko YM, Kaneshige M, Quiñónez RE, Kaneshige K, Heintz KA, Mastroianni MA, Kelley MW, Cheng SY |
| Jazyk: |
angličtina |
| Zdroj: |
Journal of the Association for Research in Otolaryngology : JARO [J Assoc Res Otolaryngol] 2002 Sep; Vol. 3 (3), pp. 279-88. Date of Electronic Publication: 2002 Feb 27. |
| DOI: |
10.1007/s101620010092 |
| Abstrakt: |
Thyroid hormone and the beta isoform of its receptor, Trb, are essential for normal development of the mammalian auditory system. We have analyzed auditory system function and structure in a mouse strain with a targeted Thrb mutation, Thrb(PV), which leads to the loss of binding of thyroid hormone (T3) to the Trb protein. Heterozygosity for the orthologous human THRB(PV) mutation and other similar mutations in human THRB cause resistance to thyroid hormone (RTH), which is occasionally associated with mild sensorineural hearing impairment. Auditory brainstem response analysis of heterozygous Thrb(PV)/+ mice demonstrates that they develop normal hearing. In contrast, Thrb(PV)/Thrb(PV) mice have severe hearing impairment that is already present at 3 weeks of age. This hearing loss is associated with disruption of postnatal morphogenesis of the tectorial membrane and organ of Corti. Comparison with the previously described phenotype of a Thrb -/- knockout strain suggests that Thrb(PV) disrupts the function of other genes that are critical for development and/or maintenance of these structures. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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