TY - JOUR
T1 - Tryptophan-rich basic protein (WRB) mediates insertion of the tail-anchored protein otoferlin and is required for hair cell exocytosis and hearing
AU - Vogl, Christian
AU - Panou, Iliana
AU - Yamanbaeva, Gulnara
AU - Wichmann, Carolin
AU - Mangosing, Sara J.
AU - Vilardi, Fabio
AU - Indzhykulian, Artur A.
AU - Pangršič, Tina
AU - Santarelli, Rosamaria
AU - Rodriguez-Ballesteros, Montserrat
AU - Weber, Thomas
AU - Jung, Sangyong
AU - Cardenas, Elena
AU - Wu, Xudong
AU - Wojcik, Sonja M.
AU - Kwan, Kelvin
AU - del Castillo, Ignacio
AU - Schwappach, Blanche
AU - Strenzke, Nicola
AU - Corey, David P.
AU - Lin, Shuh Yow
AU - Moser, Tobias
N1 - Funding Information:
We thank N. Herrmann, S. Gerke, and C. Senger-Freitag for expert technical assistance. Moreover, we would like to extend our gratitude to Y. Li and B. Derfler for genotyping/maintaining the mouse colony; D.S. Zhang, P. Niksch, and B. Shrestha for tissue dissection; D. Scheffer for initial Vglut3-ires-Cre expression patterning; W. Fowle (Northeastern University) for the access to the SEM facility; and J Santini for microscopy facility (UCSD, supported by NIH NS047101). This work was supported by grants of the German Research Foundation through the Collaborative Research Center 889 (project A2 to T.M., A6 to N.S. and A7 to C.W.) and the Priority Program 1608 (to T.M. and N.S.), by the Center for Molecular Physiology of the Brain (FZT-103 to T.M.), and the Leibniz Program (to T.M.), by Deafness Research Foundation, and UCSD Foundation grants (to S-Y.L., S.M., and E.C.) by National Institutes of Health (NIH) grants R01-DC000304 and R01-DC002281 (to D.P.C.) and of the Instituto de Salud Carlos III, Madrid, Spain (FIS PI14/01162, Plan Estatal de I+D+I 2013?2016, with co-funding from the European Regional Development Fund, to I.C.). D.P.C. is an investigator of the Howard Hughes Medical Institute.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - The transmembrane recognition complex (TRC40) pathway mediates the insertion of tail-anchored (TA) proteins into membranes. Here, we demonstrate that otoferlin, a TA protein essential for hair cell exocytosis, is inserted into the endoplasmic reticulum (ER) via the TRC40 pathway. We mutated the TRC40 receptor tryptophan-rich basic protein (Wrb) in hair cells of zebrafish and mice and studied the impact of defective TA protein insertion. Wrb disruption reduced otoferlin levels in hair cells and impaired hearing, which could be restored in zebrafish by transgenic Wrb rescue and otoferlin overexpression. Wrb-deficient mouse inner hair cells (IHCs) displayed normal numbers of afferent synapses, Ca2+ channels, and membrane-proximal vesicles, but contained fewer ribbon-associated vesicles. Patch-clamp of IHCs revealed impaired synaptic vesicle replenishment. In vivo recordings from postsynaptic spiral ganglion neurons showed a use-dependent reduction in sound-evoked spiking, corroborating the notion of impaired IHC vesicle replenishment. A human mutation affecting the transmembrane domain of otoferlin impaired its ER targeting and caused an auditory synaptopathy. We conclude that the TRC40 pathway is critical for hearing and propose that otoferlin is an essential substrate of this pathway in hair cells.
AB - The transmembrane recognition complex (TRC40) pathway mediates the insertion of tail-anchored (TA) proteins into membranes. Here, we demonstrate that otoferlin, a TA protein essential for hair cell exocytosis, is inserted into the endoplasmic reticulum (ER) via the TRC40 pathway. We mutated the TRC40 receptor tryptophan-rich basic protein (Wrb) in hair cells of zebrafish and mice and studied the impact of defective TA protein insertion. Wrb disruption reduced otoferlin levels in hair cells and impaired hearing, which could be restored in zebrafish by transgenic Wrb rescue and otoferlin overexpression. Wrb-deficient mouse inner hair cells (IHCs) displayed normal numbers of afferent synapses, Ca2+ channels, and membrane-proximal vesicles, but contained fewer ribbon-associated vesicles. Patch-clamp of IHCs revealed impaired synaptic vesicle replenishment. In vivo recordings from postsynaptic spiral ganglion neurons showed a use-dependent reduction in sound-evoked spiking, corroborating the notion of impaired IHC vesicle replenishment. A human mutation affecting the transmembrane domain of otoferlin impaired its ER targeting and caused an auditory synaptopathy. We conclude that the TRC40 pathway is critical for hearing and propose that otoferlin is an essential substrate of this pathway in hair cells.
KW - deafness
KW - endoplasmic reticulum
KW - protein targeting
KW - synapse
KW - tail-anchored protein
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U2 - 10.15252/embj.201593565
DO - 10.15252/embj.201593565
M3 - Article
C2 - 27458190
AN - SCOPUS:84979518179
VL - 35
SP - 2536
EP - 2552
JO - EMBO Journal
JF - EMBO Journal
SN - 0261-4189
IS - 23
ER -