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Volumn 111, Issue 35, 2014, Pages 12907-12912

Tip-link protein protocadherin 15 interacts with transmembrane channel-like proteins TMC1 and TMC2

Author keywords

[No Author keywords available]

Indexed keywords

ANIMALS; ANIMALS, GENETICALLY MODIFIED; CADHERINS; EVOLUTION, MOLECULAR; GENE EXPRESSION REGULATION, DEVELOPMENTAL; HAIR CELLS, AUDITORY; HAIR CELLS, VESTIBULAR; HEK293 CELLS; HUMANS; MECHANOTRANSDUCTION, CELLULAR; MEMBRANE PROTEINS; MICE; PHYLOGENY; PROTEIN PRECURSORS; TWO-HYBRID SYSTEM TECHNIQUES; ZEBRAFISH; ZEBRAFISH PROTEINS;

EID: 84907228023     PISSN: 00278424     EISSN: 10916490     Source Type: Journal    
DOI: 10.1073/pnas.1402152111     Document Type: Article
Times cited : (128)

References (31)
  • 2
    • 0034968358 scopus 로고    scopus 로고
    • Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
    • Ahmed ZM, et al. (2001) Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F. Am J Hum Genet 69(1):25-34.
    • (2001) Am J Hum Genet , vol.69 , Issue.1 , pp. 25-34
    • Ahmed, Z.M.1
  • 3
    • 0035421436 scopus 로고    scopus 로고
    • Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
    • Alagramam KN, et al. (2001) Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F. Hum Mol Genet 10(16):1709-1718.
    • (2001) Hum Mol Genet , vol.10 , Issue.16 , pp. 1709-1718
    • Alagramam, K.N.1
  • 4
    • 0035159856 scopus 로고    scopus 로고
    • The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
    • Alagramam KN, et al. (2001) The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene. Nat Genet 27(1):99-102.
    • (2001) Nat Genet , vol.27 , Issue.1 , pp. 99-102
    • Alagramam, K.N.1
  • 5
    • 14044258529 scopus 로고    scopus 로고
    • Duplicated genes with split functions: Independent roles of protocadherin15 orthologues in zebrafish hearing and vision
    • Seiler C, et al. (2005) Duplicated genes with split functions: Independent roles of protocadherin15 orthologues in zebrafish hearing and vision. Development 132(3):615-623.
    • (2005) Development , vol.132 , Issue.3 , pp. 615-623
    • Seiler, C.1
  • 6
    • 34548509448 scopus 로고    scopus 로고
    • Cadherin 23 and protocadherin 15 interact to form tiplink filaments in sensory hair cells
    • Kazmierczak P, et al. (2007) Cadherin 23 and protocadherin 15 interact to form tiplink filaments in sensory hair cells. Nature 449(7158):87-91.
    • (2007) Nature , vol.449 , Issue.7158 , pp. 87-91
    • Kazmierczak, P.1
  • 7
    • 79955394371 scopus 로고    scopus 로고
    • Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells
    • Alagramam KN, et al. (2011) Mutations in protocadherin 15 and cadherin 23 affect tip links and mechanotransduction in mammalian sensory hair cells. PLoS One 6(4):e19183.
    • (2011) PLoS One , vol.6 , Issue.4
    • Alagramam, K.N.1
  • 8
    • 65549128486 scopus 로고    scopus 로고
    • Localization of inner hair cell mechanotransducer channels using high-speed calcium imaging
    • Beurg M, Fettiplace R, Nam J-H, Ricci AJ (2009) Localization of inner hair cell mechanotransducer channels using high-speed calcium imaging. Nat Neurosci 12(5):553-558.
    • (2009) Nat Neurosci , vol.12 , Issue.5 , pp. 553-558
    • Beurg, M.1    Fettiplace, R.2    Nam, J.-H.3    Ricci, A.J.4
  • 9
    • 77957918022 scopus 로고    scopus 로고
    • Asymmetric distribution of cadherin 23 and protocadherin 15 in the kinocilial links of avian sensory hair cells
    • Goodyear RJ, Forge A, Legan PK, Richardson GP (2010) Asymmetric distribution of cadherin 23 and protocadherin 15 in the kinocilial links of avian sensory hair cells. J Comp Neurol 518(21):4288-4297.
    • (2010) J Comp Neurol , vol.518 , Issue.21 , pp. 4288-4297
    • Goodyear, R.J.1    Forge, A.2    Legan, P.K.3    Richardson, G.P.4
  • 10
    • 84881559173 scopus 로고    scopus 로고
    • TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner ear
    • Pan B, et al. (2013) TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner ear. Neuron 79(3):504-515.
    • (2013) Neuron , vol.79 , Issue.3 , pp. 504-515
    • Pan, B.1
  • 11
    • 9444261862 scopus 로고    scopus 로고
    • TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteins
    • Keresztes G, Mutai H, Heller S (2003) TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteins. BMC Genomics 4(1):24.
    • (2003) BMC Genomics , vol.4 , Issue.1 , pp. 24
    • Keresztes, G.1    Mutai, H.2    Heller, S.3
  • 12
    • 77957254987 scopus 로고    scopus 로고
    • Topology of transmembrane channel-like gene 1 protein
    • Labay V, Weichert RM, Makishima T, Griffith AJ (2010) Topology of transmembrane channel-like gene 1 protein. Biochemistry 49(39):8592-8598.
    • (2010) Biochemistry , vol.49 , Issue.39 , pp. 8592-8598
    • Labay, V.1    Weichert, R.M.2    Makishima, T.3    Griffith, A.J.4
  • 13
    • 84874683479 scopus 로고    scopus 로고
    • tmc-1 encodes a sodiumsensitive channel required for salt chemosensation in C. Elegans
    • Chatzigeorgiou M, Bang S, Hwang SW, Schafer WR (2013) tmc-1 encodes a sodiumsensitive channel required for salt chemosensation in C. elegans. Nature 494(7435):95-99.
    • (2013) Nature , vol.494 , Issue.7435 , pp. 95-99
    • Chatzigeorgiou, M.1    Bang, S.2    Hwang, S.W.3    Schafer, W.R.4
  • 14
    • 0036510053 scopus 로고    scopus 로고
    • Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function
    • Kurima K, et al. (2002) Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function. Nat Genet 30(3):277-284.
    • (2002) Nat Genet , vol.30 , Issue.3 , pp. 277-284
    • Kurima, K.1
  • 15
    • 0036509711 scopus 로고    scopus 로고
    • Beethoven, A mouse model for dominant, progressive hearing loss DFNA36
    • Vreugde S, et al. (2002) Beethoven, a mouse model for dominant, progressive hearing loss DFNA36. Nat Genet 30(3):257-258.
    • (2002) Nat Genet , vol.30 , Issue.3 , pp. 257-258
    • Vreugde, S.1
  • 16
    • 84860491233 scopus 로고    scopus 로고
    • Autosomal recessive nonsyndromic deafness genes: A review
    • Duman D, Tekin M (2012) Autosomal recessive nonsyndromic deafness genes: A review. Front Biosci (Landmark Ed) 17:2213-2236.
    • (2012) Front Biosci (Landmark Ed) , vol.17 , pp. 2213-2236
    • Duman, D.1    Tekin, M.2
  • 17
    • 84055217017 scopus 로고    scopus 로고
    • Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes
    • Kawashima Y, et al. (2011) Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes. J Clin Invest 121(12):4796-4809.
    • (2011) J Clin Invest , vol.121 , Issue.12 , pp. 4796-4809
    • Kawashima, Y.1
  • 18
    • 84872226774 scopus 로고    scopus 로고
    • Developmental changes in the cochlear hair cell mechanotransducer channel and their regulation by transmembrane channel-like proteins
    • Kim KX, Fettiplace R (2013) Developmental changes in the cochlear hair cell mechanotransducer channel and their regulation by transmembrane channel-like proteins. J Gen Physiol 141(1):141-148.
    • (2013) J Gen Physiol , vol.141 , Issue.1 , pp. 141-148
    • Kim, K.X.1    Fettiplace, R.2
  • 19
    • 84887556160 scopus 로고    scopus 로고
    • The role of transmembrane channel-like proteins in the operation of hair cell mechanotransducer channels
    • Kim KX, et al. (2013) The role of transmembrane channel-like proteins in the operation of hair cell mechanotransducer channels. J Gen Physiol 142(5):493-505.
    • (2013) J Gen Physiol , vol.142 , Issue.5 , pp. 493-505
    • Kim, K.X.1
  • 20
    • 84899479553 scopus 로고    scopus 로고
    • Transduction without tip links in cochlear hair cells is mediated by ion channels with permeation properties distinct from those of the mechanoelectrical transducer channel
    • Marcotti W, et al. (2014) Transduction without tip links in cochlear hair cells is mediated by ion channels with permeation properties distinct from those of the mechanoelectrical transducer channel. J Neurosci 34(16):5505-5514.
    • (2014) J Neurosci , vol.34 , Issue.16 , pp. 5505-5514
    • Marcotti, W.1
  • 21
    • 77954249974 scopus 로고    scopus 로고
    • Detecting interactions with membrane proteins using a membrane two-hybrid assay in yeast
    • Snider J, et al. (2010) Detecting interactions with membrane proteins using a membrane two-hybrid assay in yeast. Nat Protoc 5(7):1281-1293.
    • (2010) Nat Protoc , vol.5 , Issue.7 , pp. 1281-1293
    • Snider, J.1
  • 22
    • 33745960481 scopus 로고    scopus 로고
    • The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15
    • Ahmed ZM, et al. (2006) The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15. J Neurosci 26(26):7022-7034.
    • (2006) J Neurosci , vol.26 , Issue.26 , pp. 7022-7034
    • Ahmed, Z.M.1
  • 23
    • 34548639083 scopus 로고    scopus 로고
    • Promoter, alternative splice forms, and genomic structure of protocadherin 15
    • Alagramam KN, et al. (2007) Promoter, alternative splice forms, and genomic structure of protocadherin 15. Genomics 90(4):482-492.
    • (2007) Genomics , vol.90 , Issue.4 , pp. 482-492
    • Alagramam, K.N.1
  • 24
    • 0026356891 scopus 로고
    • Predicting coiled coils from protein sequences
    • Lupas A, Van Dyke M, Stock J (1991) Predicting coiled coils from protein sequences. Science 252(5009):1162-1164.
    • (1991) Science , vol.252 , Issue.5009 , pp. 1162-1164
    • Lupas, A.1    Van Dyke, M.2    Stock, J.3
  • 25
    • 84865085814 scopus 로고    scopus 로고
    • 2+ and diacylglycerol signaling in living cells
    • 2+ and diacylglycerol signaling in living cells. PLoS One 7(8):e42791.
    • (2012) PLoS One , vol.7 , Issue.8
    • Tewson, P.1
  • 26
    • 84865077999 scopus 로고    scopus 로고
    • Kinocilia mediate mechanosensitivity in developing zebrafish hair cells
    • Kindt KS, Finch G, Nicolson T (2012) Kinocilia mediate mechanosensitivity in developing zebrafish hair cells. Dev Cell 23(2):329-341.
    • (2012) Dev Cell , vol.23 , Issue.2 , pp. 329-341
    • Kindt, K.S.1    Finch, G.2    Nicolson, T.3
  • 27
    • 40849106619 scopus 로고    scopus 로고
    • Quiet as a mouse: Dissecting the molecular and genetic basis of hearing
    • Brown SDM, Hardisty-Hughes RE, Mburu P (2008) Quiet as a mouse: Dissecting the molecular and genetic basis of hearing. Nat Rev Genet 9(4):277-290.
    • (2008) Nat Rev Genet , vol.9 , Issue.4 , pp. 277-290
    • Brown, S.D.M.1    Hardisty-Hughes, R.E.2    Mburu, P.3
  • 28
    • 84870872561 scopus 로고    scopus 로고
    • TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells
    • Xiong W, et al. (2012) TMHS is an integral component of the mechanotransduction machinery of cochlear hair cells. Cell 151(6):1283-1295.
    • (2012) Cell , vol.151 , Issue.6 , pp. 1283-1295
    • Xiong, W.1
  • 29
    • 79955420225 scopus 로고    scopus 로고
    • Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain
    • Webb SW, et al. (2011) Regulation of PCDH15 function in mechanosensory hair cells by alternative splicing of the cytoplasmic domain. Development 138(8):1607-1617.
    • (2011) Development , vol.138 , Issue.8 , pp. 1607-1617
    • Webb, S.W.1
  • 30
    • 38149126474 scopus 로고    scopus 로고
    • High-resolution in situ hybridization to whole-mount zebrafish embryos
    • Thisse C, Thisse B (2008) High-resolution in situ hybridization to whole-mount zebrafish embryos. Nat Protoc 3(1):59-69.
    • (2008) Nat Protoc , vol.3 , Issue.1 , pp. 59-69
    • Thisse, C.1    Thisse, B.2
  • 31
    • 39849091711 scopus 로고    scopus 로고
    • Vesicular glutamate transporter 3 is required for synaptic transmission in zebrafish hair cells
    • Obholzer N, et al. (2008) Vesicular glutamate transporter 3 is required for synaptic transmission in zebrafish hair cells. J Neurosci 28(9):2110-2118.
    • (2008) J Neurosci , vol.28 , Issue.9 , pp. 2110-2118
    • Obholzer, N.1


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