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</script>Drosophila Auditory Organ Genes and Genetic Hearing Defects
pmid: 22939627
Drosophila Auditory Organ Genes and Genetic Hearing Defects
The Drosophila auditory organ shares equivalent transduction mechanisms with vertebrate hair cells, and both are specified by atonal family genes. Using a whole-organ knockout strategy based on atonal, we have identified 274 Drosophila auditory organ genes. Only four of these genes had previously been associated with fly hearing, yet one in five of the genes that we identified has a human cognate that is implicated in hearing disorders. Mutant analysis of 42 genes shows that more than half of them contribute to auditory organ function, with phenotypes including hearing loss, auditory hypersusceptibility, and ringing ears. We not only discover ion channels and motors important for hearing, but also show that auditory stimulus processing involves chemoreceptor proteins as well as phototransducer components. Our findings demonstrate mechanosensory roles for ionotropic receptors and visual rhodopsins and indicate that different sensory modalities utilize common signaling cascades.
- Max Planck Institute of Neurobiology Germany
- University of Göttingen Germany
- Max Planck Institute of Experimental Medicine Germany
- Max Planck Society Germany
- Max Planck Institute for Multidisciplinary Sciences Germany
Rhodopsin, Biochemistry, Genetics and Molecular Biology(all), Nerve Tissue Proteins, Axonemal Dyneins, Ion Channels, Transient Receptor Potential Channels, Hearing, Hair Cells, Auditory, Basic Helix-Loop-Helix Transcription Factors, Animals, Drosophila Proteins, Drosophila, Oligonucleotide Array Sequence Analysis, Signal Transduction
Rhodopsin, Biochemistry, Genetics and Molecular Biology(all), Nerve Tissue Proteins, Axonemal Dyneins, Ion Channels, Transient Receptor Potential Channels, Hearing, Hair Cells, Auditory, Basic Helix-Loop-Helix Transcription Factors, Animals, Drosophila Proteins, Drosophila, Oligonucleotide Array Sequence Analysis, Signal Transduction
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