Severe hearing loss in Dlxl mutant mice.

Daniel B Polley; Inma Cobos; Michael M Merzenich; John L R Rubenstein

doi:10.1016/j.heares.2006.02.008

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Severe hearing loss in Dlxl mutant mice.

Daniel B Polley·Inma Cobos·Michael M Merzenich·John L R Rubenstein

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Abstract

The Dlx homeobox gene family participates in regulating middle and inner ear development. A significant role for Dlxl, in particular,has been demonstrated in the development of the middle ear ossicles, but the functional consequences of Dlx.l gene mutation on hearing thresholds has not been assessed. The present study characterizes auditory brainstem responses to click and tonal stimuli in a non-lethal variant of a Dlxl gene knockout. We found that peripheral hearing thresholds for click and tonal stimuli were significantly elevated in homozygous Dlxl knockout (Dlxl-/ ) compared to both heterozygous (Dlxl+/ ) and wild type (Dlxl+/+) mice. Thus, abnormal mor-phogenesis of the incus and stapes that has been documented previously with histological measures is now known to result in a severe peripheral hearing deficit.

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Animals Ear Ossicles Evoked Potentials, Auditory, Brain Stem Hearing Loss, Sensorineural Homeodomain Proteins Mice Mutation Severity of Illness Index Transcription Factors Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

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Daniel B Polley, Inma Cobos, Michael M Merzenich, John L R Rubenstein. 2006. Severe hearing loss in Dlxl mutant mice.. https://doi.org/10.1016/j.heares.2006.02.008

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