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Erschienen in: Journal of the Association for Research in Otolaryngology 4/2010

Open Access 01.12.2010 | Research Article

Identification of the Hair Cell Soma-1 Antigen, HCS-1, as Otoferlin

verfasst von: Richard J. Goodyear, P. Kevin Legan, Jeffrey R. Christiansen, Bei Xia, Julia Korchagina, Jonathan E. Gale, Mark E. Warchol, Jeffrey T. Corwin, Guy P. Richardson

Erschienen in: Journal of the Association for Research in Otolaryngology | Ausgabe 4/2010

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Abstract

Hair cells, the mechanosensitive receptor cells of the inner ear, are critical for our senses of hearing and balance. The small number of these receptor cells in the inner ear has impeded the identification and characterization of proteins important for hair cell function. The binding specificity of monoclonal antibodies provides a means for identifying hair cell-specific proteins and isolating them for further study. We have generated a monoclonal antibody, termed hair cell soma-1 (HCS-1), which specifically immunolabels hair cells in at least five vertebrate classes, including sharks and rays, bony fish, amphibians, birds, and mammals. We used HCS-1 to immunoprecipitate the cognate antigen and identified it as otoferlin, a member of the ferlin protein family. Mutations in otoferlin underlie DFNB9, a recessive, nonsyndromic form of prelingual deafness characterized as an auditory neuropathy. Using immunocytochemistry, we find that otoferlin is associated with the entire basolateral membrane of the hair cells and with vesicular structures distributed throughout most of the hair cell cytoplasm. Biochemical assays indicate that otoferlin is tightly associated with membranes, as it is not solubilized by alterations in calcium or salt concentrations. HCS-1 immunolabeling does not co-localize with ribeye, a constituent of synaptic ribbons, suggesting that otoferlin may, in addition to its proposed function in synaptic vesicle release, play additional roles in hair cells.
Literatur
Zurück zum Zitat Ahmed ZM, Goodyear R, Riazuddin S, Lagziel A, Legan PK, Behra M, Burgess SM, Lilley KS, Wilcox ER, Riazuddin S, Griffith AJ, Frolenkov GI, Belyantseva IA, Richardson GP, Friedman TB (2006) The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15. J Neurosci 26:7022–7034CrossRefPubMed Ahmed ZM, Goodyear R, Riazuddin S, Lagziel A, Legan PK, Behra M, Burgess SM, Lilley KS, Wilcox ER, Riazuddin S, Griffith AJ, Frolenkov GI, Belyantseva IA, Richardson GP, Friedman TB (2006) The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15. J Neurosci 26:7022–7034CrossRefPubMed
Zurück zum Zitat Bansal D, Campbell KP (2004) Dysferlin and the plasma membrane repair in muscular dystrophy. Trends Cell Biol 14:206–213CrossRefPubMed Bansal D, Campbell KP (2004) Dysferlin and the plasma membrane repair in muscular dystrophy. Trends Cell Biol 14:206–213CrossRefPubMed
Zurück zum Zitat Bartolami S, Goodyear R, Richardson G (1991) Appearance and distribution of the 275 kD hair-cell antigen during development of the avian inner ear. J Comp Neurol 314:777–788CrossRefPubMed Bartolami S, Goodyear R, Richardson G (1991) Appearance and distribution of the 275 kD hair-cell antigen during development of the avian inner ear. J Comp Neurol 314:777–788CrossRefPubMed
Zurück zum Zitat Beurg M, Safieddine S, Roux I, Bouleau Y, Petit C, Dulon D (2008) Calcium- and otoferlin-dependent exocytosis by immature outer hair cells. J Neurosci 28:1798–1803CrossRefPubMed Beurg M, Safieddine S, Roux I, Bouleau Y, Petit C, Dulon D (2008) Calcium- and otoferlin-dependent exocytosis by immature outer hair cells. J Neurosci 28:1798–1803CrossRefPubMed
Zurück zum Zitat Bird JE, Daudet N, Warchol ME, Gale JE (2010) Supporting cells eliminate dying sensory hair cells to maintain epithelial integrity in the avian inner ear. J Neurosci (in press) Bird JE, Daudet N, Warchol ME, Gale JE (2010) Supporting cells eliminate dying sensory hair cells to maintain epithelial integrity in the avian inner ear. J Neurosci (in press)
Zurück zum Zitat Blasiole B, Canfield VA, Vollrath MA, Huss D, Mohideen MA, Dickman JD, Cheng KC, Fekete DM, Levenson R (2006) Separate Na,K-ATPase genes are required for otolith formation and semicircular canal development in zebrafish. Dev Biol 294:148–160CrossRefPubMed Blasiole B, Canfield VA, Vollrath MA, Huss D, Mohideen MA, Dickman JD, Cheng KC, Fekete DM, Levenson R (2006) Separate Na,K-ATPase genes are required for otolith formation and semicircular canal development in zebrafish. Dev Biol 294:148–160CrossRefPubMed
Zurück zum Zitat Brandt N, Kuhn S, Munkner S, Braig C, Winter H, Blin N, Vonthein R, Knipper M, Engel J (2007) Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells. J Neurosci 27:3174–3186CrossRefPubMed Brandt N, Kuhn S, Munkner S, Braig C, Winter H, Blin N, Vonthein R, Knipper M, Engel J (2007) Thyroid hormone deficiency affects postnatal spiking activity and expression of Ca2+ and K+ channels in rodent inner hair cells. J Neurosci 27:3174–3186CrossRefPubMed
Zurück zum Zitat Bricaud O, Collazo A (2006) The transcription factor six1 inhibits neuronal and promotes hair cell fate in the developing zebrafish (Danio rerio) inner ear. J Neurosci 26:10438–10451CrossRefPubMed Bricaud O, Collazo A (2006) The transcription factor six1 inhibits neuronal and promotes hair cell fate in the developing zebrafish (Danio rerio) inner ear. J Neurosci 26:10438–10451CrossRefPubMed
Zurück zum Zitat Cho W, Stahelin RV (2006) Membrane binding and subcellular targeting of C2 domains. Biochim Biophys Acta 1761:838–849PubMed Cho W, Stahelin RV (2006) Membrane binding and subcellular targeting of C2 domains. Biochim Biophys Acta 1761:838–849PubMed
Zurück zum Zitat Choi BY, Ahmed ZM, Riazuddin S, Bhinder MA, Shahzad M, Husnain T, Riazuddin S, Griffith AJ, Friedman TB (2009) Identities and frequencies of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan. Clin Gent 75:237–243CrossRef Choi BY, Ahmed ZM, Riazuddin S, Bhinder MA, Shahzad M, Husnain T, Riazuddin S, Griffith AJ, Friedman TB (2009) Identities and frequencies of the otoferlin gene (OTOF) causing DFNB9 deafness in Pakistan. Clin Gent 75:237–243CrossRef
Zurück zum Zitat Daudet N, Lewis J (2005) Two contrasting roles for Notch activity in chick inner ear development: specification of prosensory patches and lateral inhibition of hair-cell differentiation. Development 132:541–551CrossRefPubMed Daudet N, Lewis J (2005) Two contrasting roles for Notch activity in chick inner ear development: specification of prosensory patches and lateral inhibition of hair-cell differentiation. Development 132:541–551CrossRefPubMed
Zurück zum Zitat Dikgraaf S (1933) Untersuchungen uber die Funktion der seitenorgane an fischen. J Comp Physiol A 20:162–214 Dikgraaf S (1933) Untersuchungen uber die Funktion der seitenorgane an fischen. J Comp Physiol A 20:162–214
Zurück zum Zitat Dumont RA, Lins U, Filoteo AG, Penniston JT, Kachar B, Gillespie PG (2001) Plasma membrane Ca2+-ATPase isoform 2a is the PMCA of hair bundles. J Neurosci 21:5066–5078PubMed Dumont RA, Lins U, Filoteo AG, Penniston JT, Kachar B, Gillespie PG (2001) Plasma membrane Ca2+-ATPase isoform 2a is the PMCA of hair bundles. J Neurosci 21:5066–5078PubMed
Zurück zum Zitat Ebermann I, Walger M, Scholl HP, Charbel Issa P, Luke C, Nurnberg G, Lang-Roth R, Becker C, Nurnberg P, Bolz HJ (2007) Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction. Hum Mutat 28:571–2007CrossRefPubMed Ebermann I, Walger M, Scholl HP, Charbel Issa P, Luke C, Nurnberg G, Lang-Roth R, Becker C, Nurnberg P, Bolz HJ (2007) Truncating mutation of the DFNB59 gene causes cochlear hearing impairment and central vestibular dysfunction. Hum Mutat 28:571–2007CrossRefPubMed
Zurück zum Zitat Forlano PM, Deitcher DL, Bass AH (2005) Distribution of estrogen receptor alpha mRNA in the brain and inner ear of a vocal fish with comparisons to sites of aromatase expression. J Comp Neurol 483:91–113CrossRefPubMed Forlano PM, Deitcher DL, Bass AH (2005) Distribution of estrogen receptor alpha mRNA in the brain and inner ear of a vocal fish with comparisons to sites of aromatase expression. J Comp Neurol 483:91–113CrossRefPubMed
Zurück zum Zitat Gale JE, Meyers JR, Corwin JT (2000) Solitary hair cells are distributed throughout the extramacular epithelium in the bullfrog’s saccule. J Assoc Res Otolaryngol 1:172–182CrossRefPubMed Gale JE, Meyers JR, Corwin JT (2000) Solitary hair cells are distributed throughout the extramacular epithelium in the bullfrog’s saccule. J Assoc Res Otolaryngol 1:172–182CrossRefPubMed
Zurück zum Zitat Gale JE, Meyers JR, Periasamy A, Corwin JT (2002) Survival of bundleless hair cells and subsequent bundle replacement in the bullfrog’s saccule. J Neurobiol 50:81–92CrossRefPubMed Gale JE, Meyers JR, Periasamy A, Corwin JT (2002) Survival of bundleless hair cells and subsequent bundle replacement in the bullfrog’s saccule. J Neurobiol 50:81–92CrossRefPubMed
Zurück zum Zitat Girod DA, Ducker LG, Rubel EW (1989) Possible precursors of regenerated hair cells in the avian cochlea following acoustic trauma. Hear Res 42:175–194CrossRefPubMed Girod DA, Ducker LG, Rubel EW (1989) Possible precursors of regenerated hair cells in the avian cochlea following acoustic trauma. Hear Res 42:175–194CrossRefPubMed
Zurück zum Zitat Goodyear R, Richardson G (1992) Distribution of the 275 kD hair cell antigen and cell surface specializations on auditory and vestibular hair bundles in the chicken inner ear. J Comp Neurol 325:243–256CrossRefPubMed Goodyear R, Richardson G (1992) Distribution of the 275 kD hair cell antigen and cell surface specializations on auditory and vestibular hair bundles in the chicken inner ear. J Comp Neurol 325:243–256CrossRefPubMed
Zurück zum Zitat Goodyear R, Richardson G (1997) Pattern formation in the basilar papilla:evidence for cell rearrangement. J Neurosci 17:6239–6231 Goodyear R, Richardson G (1997) Pattern formation in the basilar papilla:evidence for cell rearrangement. J Neurosci 17:6239–6231
Zurück zum Zitat Goodyear R, Richardson G (1999) The ankle-link antigen: an epitope sensitive to calcium chelation associated with the hair-cell surface and the calycal processes of photoreceptors. J Neurosci 19:3761–3772PubMed Goodyear R, Richardson G (1999) The ankle-link antigen: an epitope sensitive to calcium chelation associated with the hair-cell surface and the calycal processes of photoreceptors. J Neurosci 19:3761–3772PubMed
Zurück zum Zitat Goodyear RJ, Richardson GP (2003) A novel antigen sensitive to calcium chelation that is associated with the tip links and kinocilial links of sensory hair bundles. J Neurosci 23:4878–4887PubMed Goodyear RJ, Richardson GP (2003) A novel antigen sensitive to calcium chelation that is associated with the tip links and kinocilial links of sensory hair bundles. J Neurosci 23:4878–4887PubMed
Zurück zum Zitat Goodyear RJ, Legan PK, Wright MB, Marcotti W, Oganesian A, Coats SA, Booth CJ, Kros CJ, Seifert RA, Bowen-Pope DF, Richardson GP (2003) A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles. J Neurosci 23:9208–9219PubMed Goodyear RJ, Legan PK, Wright MB, Marcotti W, Oganesian A, Coats SA, Booth CJ, Kros CJ, Seifert RA, Bowen-Pope DF, Richardson GP (2003) A receptor-like inositol lipid phosphatase is required for the maturation of developing cochlear hair bundles. J Neurosci 23:9208–9219PubMed
Zurück zum Zitat Griffiths G, Hoflack B, Simons K, Mellman I, Kornfeld S (1988) The mannose 6-phosphate receptor and the biogenesis of lysosomes. Cell 52:329–341CrossRefPubMed Griffiths G, Hoflack B, Simons K, Mellman I, Kornfeld S (1988) The mannose 6-phosphate receptor and the biogenesis of lysosomes. Cell 52:329–341CrossRefPubMed
Zurück zum Zitat Heidrych P, Zimmerman U, Kuhn S, Franz C, Engel J, Dunckner SV, Hirt B, Pusch CM, Ruth P, Pfister M, Marcotti W, Blin N, Knipper M (2009) Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell. Hum Mol Genet 18:2779–2790CrossRefPubMed Heidrych P, Zimmerman U, Kuhn S, Franz C, Engel J, Dunckner SV, Hirt B, Pusch CM, Ruth P, Pfister M, Marcotti W, Blin N, Knipper M (2009) Otoferlin interacts with myosin VI: implications for maintenance of the basolateral synaptic structure of the inner hair cell. Hum Mol Genet 18:2779–2790CrossRefPubMed
Zurück zum Zitat Hu Z, Corwin JT (2007) Inner ear hair cells produced in vitro by a mesenchymal-to-epithelial transition. Proc Natl Acad Sci USA 104:16675–16680CrossRefPubMed Hu Z, Corwin JT (2007) Inner ear hair cells produced in vitro by a mesenchymal-to-epithelial transition. Proc Natl Acad Sci USA 104:16675–16680CrossRefPubMed
Zurück zum Zitat Issa NP, Hudspeth AJ (1996) Characterization of fluo-3 labeling of dense bodies at the hair cell’s presynaptic active zone. J Neurocytol 25:257–266CrossRefPubMed Issa NP, Hudspeth AJ (1996) Characterization of fluo-3 labeling of dense bodies at the hair cell’s presynaptic active zone. J Neurocytol 25:257–266CrossRefPubMed
Zurück zum Zitat Judice TN, Nelson NC, Beisel CL, Delimont DC, Fritzsch B, Beisel KW (2002) Cochlear whole mount in situ hybridization: identification of longitudinal and radial gradients. Brain Res Brain Res Protoc 9:65–76CrossRefPubMed Judice TN, Nelson NC, Beisel CL, Delimont DC, Fritzsch B, Beisel KW (2002) Cochlear whole mount in situ hybridization: identification of longitudinal and radial gradients. Brain Res Brain Res Protoc 9:65–76CrossRefPubMed
Zurück zum Zitat LeMasurier M, Gillespie PG (2005) Hair-cell mechanotransduction and cochlear amplification. Neuron 48:403–415CrossRefPubMed LeMasurier M, Gillespie PG (2005) Hair-cell mechanotransduction and cochlear amplification. Neuron 48:403–415CrossRefPubMed
Zurück zum Zitat Lemmon MA (2008) Membrane recognition by phospholipid-binding domains. Nat Rev Mol Cell Biol 9:99–111CrossRefPubMed Lemmon MA (2008) Membrane recognition by phospholipid-binding domains. Nat Rev Mol Cell Biol 9:99–111CrossRefPubMed
Zurück zum Zitat Lenzi D, Runyeon JW, Crum J, Ellisman MH, Roberts WM (1999) Synaptic vesicle populations in saccular hair cells reconstructed by electron tomography. J Neurosci 19:119–132PubMed Lenzi D, Runyeon JW, Crum J, Ellisman MH, Roberts WM (1999) Synaptic vesicle populations in saccular hair cells reconstructed by electron tomography. J Neurosci 19:119–132PubMed
Zurück zum Zitat Longo-Guess C, Gagnon LH, Bergstrom DE, Johnson KR (2007) A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9. Hear Res 234:21–28CrossRefPubMed Longo-Guess C, Gagnon LH, Bergstrom DE, Johnson KR (2007) A missense mutation in the conserved C2B domain of otoferlin causes deafness in a new mouse model of DFNB9. Hear Res 234:21–28CrossRefPubMed
Zurück zum Zitat Lopez-Schier H, Hudspeth AJ (2005) Supernumerary neuromasts in the posterior lateral line of zebrafish lacking peripheral glia. Proc Natl Acad Sci USA 102:1496–1501CrossRefPubMed Lopez-Schier H, Hudspeth AJ (2005) Supernumerary neuromasts in the posterior lateral line of zebrafish lacking peripheral glia. Proc Natl Acad Sci USA 102:1496–1501CrossRefPubMed
Zurück zum Zitat Lopez-Schier H, Hudspeth AJ (2006) A two-step mechanism underlies the planar polarization of regenerating sensory hair cells. Proc Natl Acad Sci USA 103:18615–18620CrossRefPubMed Lopez-Schier H, Hudspeth AJ (2006) A two-step mechanism underlies the planar polarization of regenerating sensory hair cells. Proc Natl Acad Sci USA 103:18615–18620CrossRefPubMed
Zurück zum Zitat Lumpkin EA, Hudspeth AJ (1995) Detection of Ca2+ entry through mechanosensitive channels localizes the site of mechanoelectrical transduction in hair cells. Proc Natl Acad Sci USA 92:10297–10301CrossRefPubMed Lumpkin EA, Hudspeth AJ (1995) Detection of Ca2+ entry through mechanosensitive channels localizes the site of mechanoelectrical transduction in hair cells. Proc Natl Acad Sci USA 92:10297–10301CrossRefPubMed
Zurück zum Zitat Ma EY, Rubel EW, Raible DW (2008) Notch signaling regulates the extent of hair cell regeneration in the zebrafish lateral line. J Neurosci 28:2261–2273CrossRefPubMed Ma EY, Rubel EW, Raible DW (2008) Notch signaling regulates the extent of hair cell regeneration in the zebrafish lateral line. J Neurosci 28:2261–2273CrossRefPubMed
Zurück zum Zitat McGee J, Goodyear RJ, McMillan DR, Stauffer EA, Holt JR, Locke KG, Birch DG, Legan PK, White PC, Walsh EJ, Richardson GP (2006) The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles. J Neurosci 26:6543–6553CrossRefPubMed McGee J, Goodyear RJ, McMillan DR, Stauffer EA, Holt JR, Locke KG, Birch DG, Legan PK, White PC, Walsh EJ, Richardson GP (2006) The very large G-protein-coupled receptor VLGR1: a component of the ankle link complex required for the normal development of auditory hair bundles. J Neurosci 26:6543–6553CrossRefPubMed
Zurück zum Zitat Migliosi V, Modamio-Hoybjor S, Moreno-Pelayo MA, Rodriguez-Ballesteros M, Villamar M, Telleria D, Menendez I, Moreno F, Del Castillo I (2002) Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss. J Med Genet 39:502–506CrossRefPubMed Migliosi V, Modamio-Hoybjor S, Moreno-Pelayo MA, Rodriguez-Ballesteros M, Villamar M, Telleria D, Menendez I, Moreno F, Del Castillo I (2002) Q829X, a novel mutation in the gene encoding otoferlin (OTOF), is frequently found in Spanish patients with prelingual non-syndromic hearing loss. J Med Genet 39:502–506CrossRefPubMed
Zurück zum Zitat Mirghomizadeh F, Pfister M, Apaydin F, Petit C, Kupka S, Pusch CM, Zenner HP, Blin N (2002) Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness. Neurobiol Dis 10:157–164CrossRefPubMed Mirghomizadeh F, Pfister M, Apaydin F, Petit C, Kupka S, Pusch CM, Zenner HP, Blin N (2002) Substitutions in the conserved C2C domain of otoferlin cause DFNB9, a form of nonsyndromic autosomal recessive deafness. Neurobiol Dis 10:157–164CrossRefPubMed
Zurück zum Zitat Molea D, Stone JS, Rubel EW (1999) Class III beta-tubulin expression in sensory and nonsensory regions of the developing avian inner ear. J Comp Neurol 406:183–198CrossRefPubMed Molea D, Stone JS, Rubel EW (1999) Class III beta-tubulin expression in sensory and nonsensory regions of the developing avian inner ear. J Comp Neurol 406:183–198CrossRefPubMed
Zurück zum Zitat Ramakrishnan NA, Drescher MJ, Drescher DG (2009) Direct interaction of otoferlin with syntaxin 1A, SNAP-25 and the L-type voltage-gated calcium channel. J Biol Chem 16:1364–1372 Ramakrishnan NA, Drescher MJ, Drescher DG (2009) Direct interaction of otoferlin with syntaxin 1A, SNAP-25 and the L-type voltage-gated calcium channel. J Biol Chem 16:1364–1372
Zurück zum Zitat Richardson GP, Bartolami S, Russell IJ (1990) Identification of a 275-kD protein associated with the apical surfaces of sensory hair cells in the avian inner ear. J Cell Biol 110:1055–1066CrossRefPubMed Richardson GP, Bartolami S, Russell IJ (1990) Identification of a 275-kD protein associated with the apical surfaces of sensory hair cells in the avian inner ear. J Cell Biol 110:1055–1066CrossRefPubMed
Zurück zum Zitat Rodriguez-Ballesteros M, del Castillo FJ, Martin Y, Moreno-Pelayo MA, Morera C, Prieto F, Marco J, Morant A, Gallo-Teran J, Morales-Angulo C, Navas C, Trinidad G, Tapia MC, Moreno F, del Castillo I (2003) Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF). Hum Mutat 22:451–456CrossRefPubMed Rodriguez-Ballesteros M, del Castillo FJ, Martin Y, Moreno-Pelayo MA, Morera C, Prieto F, Marco J, Morant A, Gallo-Teran J, Morales-Angulo C, Navas C, Trinidad G, Tapia MC, Moreno F, del Castillo I (2003) Auditory neuropathy in patients carrying mutations in the otoferlin gene (OTOF). Hum Mutat 22:451–456CrossRefPubMed
Zurück zum Zitat Roux I, Safieddine S, Nouvian R, Grati M, Simmler MC, Bahloul A, Perfettini I, Le Gall M, Rostaing P, Hamard G, Triller A, Avan P, Moser T, Petit C (2006) Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell 127:277–289CrossRefPubMed Roux I, Safieddine S, Nouvian R, Grati M, Simmler MC, Bahloul A, Perfettini I, Le Gall M, Rostaing P, Hamard G, Triller A, Avan P, Moser T, Petit C (2006) Otoferlin, defective in a human deafness form, is essential for exocytosis at the auditory ribbon synapse. Cell 127:277–289CrossRefPubMed
Zurück zum Zitat Schmitz F, Konigstorfer A, Sudhof TC (2000) RIBEYE, a component of synaptic ribbons: a protein’s journey through evolution provides insight into synaptic ribbon function. Neuron 28:857–872CrossRefPubMed Schmitz F, Konigstorfer A, Sudhof TC (2000) RIBEYE, a component of synaptic ribbons: a protein’s journey through evolution provides insight into synaptic ribbon function. Neuron 28:857–872CrossRefPubMed
Zurück zum Zitat Schug N, Braig C, Zimmermann U, Engel J, Winter H, Ruth P, Blin N, Pfister M, Kalbacher H, Knipper M (2006) Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat. Eur J Neurosci 24:3372–3380CrossRefPubMed Schug N, Braig C, Zimmermann U, Engel J, Winter H, Ruth P, Blin N, Pfister M, Kalbacher H, Knipper M (2006) Differential expression of otoferlin in brain, vestibular system, immature and mature cochlea of the rat. Eur J Neurosci 24:3372–3380CrossRefPubMed
Zurück zum Zitat Schwander M, Sczaniecka A, Grillet N, Bailey JS, Avenarius M, Najmabadi H, Steffy BM, Federe GC, Lagler EA, Banan R, Hice R, Grabowski-Boase L, Keithley EM, Ryan AF, Housley GD, Wiltshire T, Smith RJ, Tarntino LM, Muller U (2007) A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. J Neurosci 27:2163–2173 Schwander M, Sczaniecka A, Grillet N, Bailey JS, Avenarius M, Najmabadi H, Steffy BM, Federe GC, Lagler EA, Banan R, Hice R, Grabowski-Boase L, Keithley EM, Ryan AF, Housley GD, Wiltshire T, Smith RJ, Tarntino LM, Muller U (2007) A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. J Neurosci 27:2163–2173
Zurück zum Zitat Steyger PS, Burton M, Hawkins JR, Schuff NR, Baird RA (1997) Calbindin and parvalbumin are early markers of non-mitotically regenerating hair cells in the bullfrog vestibular otolith organs. Int J Dev Neurosci 15:417–432CrossRefPubMed Steyger PS, Burton M, Hawkins JR, Schuff NR, Baird RA (1997) Calbindin and parvalbumin are early markers of non-mitotically regenerating hair cells in the bullfrog vestibular otolith organs. Int J Dev Neurosci 15:417–432CrossRefPubMed
Zurück zum Zitat Stone JS, Rubel EW (2000) Temporal, spatial, and morphologic features of hair cell regeneration in the avian basilar papilla. J Comp Neurol 417:1–16CrossRefPubMed Stone JS, Rubel EW (2000) Temporal, spatial, and morphologic features of hair cell regeneration in the avian basilar papilla. J Comp Neurol 417:1–16CrossRefPubMed
Zurück zum Zitat Taylor RR, Forge A (2005) Hair cell regeneration in sensory epithelia from the inner ear of a urodele amphibian. J Comp Neurol 484:105–120CrossRefPubMed Taylor RR, Forge A (2005) Hair cell regeneration in sensory epithelia from the inner ear of a urodele amphibian. J Comp Neurol 484:105–120CrossRefPubMed
Zurück zum Zitat Tekin M, Akcayoz D, Incesulu A (2005) A novel missense mutation in a C2 domain of OTOF results in autosomal recessive auditory neuropathy. Am J Med Genet A 138:6–10PubMed Tekin M, Akcayoz D, Incesulu A (2005) A novel missense mutation in a C2 domain of OTOF results in autosomal recessive auditory neuropathy. Am J Med Genet A 138:6–10PubMed
Zurück zum Zitat Varga R, Kelley PM, Keats BJ, Starr A, Leal SM, Cohn E, Kimberling WJ (2003) Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene. J Med Genet 40:45–50CrossRefPubMed Varga R, Kelley PM, Keats BJ, Starr A, Leal SM, Cohn E, Kimberling WJ (2003) Non-syndromic recessive auditory neuropathy is the result of mutations in the otoferlin (OTOF) gene. J Med Genet 40:45–50CrossRefPubMed
Zurück zum Zitat Varga R, Avenarius MR, Kelley PM, Keats BJ, Berlin CI, Hood LJ, Morlet TG, Brashears SM, Starr A, Cohn ES, Smith RJ, Kimberling WJ (2006) OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele. J Med Genet 43:576–581CrossRefPubMed Varga R, Avenarius MR, Kelley PM, Keats BJ, Berlin CI, Hood LJ, Morlet TG, Brashears SM, Starr A, Cohn ES, Smith RJ, Kimberling WJ (2006) OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele. J Med Genet 43:576–581CrossRefPubMed
Zurück zum Zitat Warchol ME, Speck JD (2007) Expression of GATA3 and tenascin in the avian vestibular maculae: normative patterns and changes during sensory regeneration. J Comp Neurol 500:646–657CrossRefPubMed Warchol ME, Speck JD (2007) Expression of GATA3 and tenascin in the avian vestibular maculae: normative patterns and changes during sensory regeneration. J Comp Neurol 500:646–657CrossRefPubMed
Zurück zum Zitat Yasunaga S, Grati M, Cohen-Salmon M, El-Amraoui A, Mustapha M, Salem N, El-Zir E, Loiselet J, Petit C (1999) A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness. Nat Genet 21:363–369CrossRefPubMed Yasunaga S, Grati M, Cohen-Salmon M, El-Amraoui A, Mustapha M, Salem N, El-Zir E, Loiselet J, Petit C (1999) A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness. Nat Genet 21:363–369CrossRefPubMed
Zurück zum Zitat Yasunaga S, Grati M, Chardenoux S, Smith TN, Friedman TB, Lalwani AK, Wilcox ER, Petit C (2000) OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9. Am J Hum Genet 67:591–600CrossRefPubMed Yasunaga S, Grati M, Chardenoux S, Smith TN, Friedman TB, Lalwani AK, Wilcox ER, Petit C (2000) OTOF encodes multiple long and short isoforms: genetic evidence that the long ones underlie recessive deafness DFNB9. Am J Hum Genet 67:591–600CrossRefPubMed
Metadaten
Titel
Identification of the Hair Cell Soma-1 Antigen, HCS-1, as Otoferlin
verfasst von
Richard J. Goodyear
P. Kevin Legan
Jeffrey R. Christiansen
Bei Xia
Julia Korchagina
Jonathan E. Gale
Mark E. Warchol
Jeffrey T. Corwin
Guy P. Richardson
Publikationsdatum
01.12.2010
Verlag
Springer-Verlag
Erschienen in
Journal of the Association for Research in Otolaryngology / Ausgabe 4/2010
Print ISSN: 1525-3961
Elektronische ISSN: 1438-7573
DOI
https://doi.org/10.1007/s10162-010-0231-6

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