The transmembrane inner ear (Tmie) protein is essential for normal hearing and balance in the zebrafish
Author(s) -
Michelle R. Gleason,
Aaron Nagiel,
Sophie Jamet,
Maria Vologodskaia,
Hernán LópezSchier,
A. J. Hudspeth
Publication year - 2009
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.0911632106
Subject(s) - inner ear , zebrafish , hair cell , transduction (biophysics) , biology , microbiology and biotechnology , stereocilia (inner ear) , transmembrane protein , mechanotransduction , mutant , cochlea , kinocilium , positional cloning , signal transduction , neuroscience , genetics , gene , biophysics , receptor
Little is known about the proteins that mediate mechanoelectrical transduction, the process by which acoustic and accelerational stimuli are transformed by hair cells of the inner ear into electrical signals. In our search for molecules involved in mechanotransduction, we discovered a line of deaf and uncoordinated zebrafish with defective hair-cell function. The hair cells of mutant larvae fail to incorporate fluorophores that normally traverse the transduction channels and their ears lack microphonic potentials in response to vibratory stimuli. Hair cells in the posterior lateral lines of mutants contain numerous lysosomes and have short, disordered hair bundles. Their stereocilia lack two components of the transduction apparatus, tip links and insertional plaques. Positional cloning revealed an early frameshift mutation in tmie, the zebrafish ortholog of the mammalian gene transmembrane inner ear. The mutant line therefore affords us an opportunity to investigate the role of the corresponding protein in mechanoelectrical transduction.
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