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{{for|the astronomical object|TMC-1}} | |||
{{ | {{Infobox_gene}} | ||
| | '''Transmembrane channel-like protein 1''' is a [[protein]] that in humans is encoded by the ''TMC1'' [[gene]].<ref name="Kurima_2002">{{cite journal | vauthors = Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, Khan S, Riazuddin S, Deininger PL, Hampton LL, Sullivan SL, Battey JF, Keats BJ, Wilcox ER, Friedman TB, Griffith AJ | title = Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function | journal = Nat Genet | volume = 30 | issue = 3 | pages = 277–84 | date = Mar 2002 | pmid = 11850618 | pmc = | doi = 10.1038/ng842 }}</ref><ref name="Vreugde_2002">{{cite journal | vauthors = Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP | title = Beethoven, a mouse model for dominant, progressive hearing loss DFNA36 | journal = Nat Genet | volume = 30 | issue = 3 | pages = 257–8 | year = 2002 | pmid = 11850623 | pmc = | doi = 10.1038/ng848 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: TMC1 transmembrane channel-like 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=117531| accessdate = }}</ref> TMC1 contains six transmembrane domains with both the C and N termini on the endoplasmic side of the membrane, as well as a large loop between domains 4 and 5. This topology is similar to that of [[transient receptor potential channels]] (TRPs),<ref name="Kurima_2002"/> a family of proteins involved in the perception of senses such as temperature, taste, pressure, and vision.<ref>{{cite journal | vauthors = Vriens J, Nilius B, Voets T | title = Peripheral thermosensation in mammals | journal = Nature Reviews Neuroscience | volume = 15 | issue = 9 | pages = 573–89 | year = 2014 | pmid = 25053448 | doi = 10.1038/nrn3784 }}</ref> TMC1 has been located in the post-natal mouse cochlea,<ref name="Kurima_2002"/> and knockouts for TMC1 and [[TMC2]] result in both auditory and vestibular deficits (hearing loss and balance issues) indicating TMC1 is a molecular part of auditory transduction.<ref name="pmid22105175">{{cite journal | vauthors = Kawashima Y, Géléoc GS, Kurima K, Labay V, Lelli A, Asai Y, Makishima T, Wu DK, Della Santina CC, Holt JR, Griffith AJ | title = Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes | journal = J. Clin. Invest. | volume = 121 | issue = 12 | pages = 4796–809 | year = 2011 | pmid = 22105175 | pmc = 3223072 | doi = 10.1172/JCI60405 }}</ref> | ||
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== Function == | |||
This gene is considered a member of a gene family predicted to encode [[transmembrane]] proteins. Until recently, the specific function of this gene was relatively unknown; it was only known to be required for normal function of [[hair cell|cochlear hair cells]].<ref name="entrez"/> However, new research suggests that TMC1 interacts with [[Tip link]] proteins [[PCDH15|protocadherin 15]] and [[CDH23|cadherin 23]] indicating that TMC1, along with [[TMC2]], are necessary proteins for [[hair cell]] mechanotransduction.<ref name="Maeda_2014">{{cite journal | vauthors = Maeda R, Kindt KS, Mo W, Morgan CP, Erickson T, Zhao H, Clemens-Grisham R, Barr-Gillespie PG, Nicolson T | title = Tip-link protein protocadherin 15 interacts with transmembrane channel-like proteins TMC1 and TMC2 | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 111 | issue = 35 | pages = 12907–12 | year = 2014 | pmid = 25114259 | doi = 10.1073/pnas.1402152111 | pmc=4156717}}</ref> Specifically, TMC1 and [[TMC2]] may be two pore-forming subunits of the channel that responds to tip link deflection in hair cells.<ref name="pmid23871232">{{cite journal | vauthors = Pan B, Géléoc GS, Asai Y, Horwitz GC, Kurima K, Ishikawa K, Kawashima Y, Griffith AJ, Holt JR | title = TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner ear | journal = Neuron | volume = 79 | issue = 3 | pages = 504–15 | year = 2013 | pmid = 23871232 | pmc = 3827726 | doi = 10.1016/j.neuron.2013.06.019 }}</ref> | |||
Due to its implication in cochlear hair cell function and its interaction with hair cell tip links, TMC1 is being mutated and manipulated in order to better understand the receptor while at the same time producing a molecular model for deafness. While deafness can arise at any stage of auditory processing, DFNA36 (a type of progressive hearing loss) and DFNB7/B11 (congenital hearing loss) have been specifically shown to arise from TMC1 mutations. DFNA36 results from a dominant missense mutation and DFNB7/B11 results from a recessive mutation.<ref name="Kurima_2002"/> Both have been modeled in mice, known as the Beethoven model and the dn model respectively.<ref name="Vreugde_2002"/> The TMC1 gene is located on [[chromosome 9]]q31-q21, and the dominant mutation associated with DFNA36 occurs at amino acid 572<ref name="Kitajiri_2007">{{cite journal | vauthors = Kitajiri S, Makishima T, Friedman TB, Griffith AJ | title = A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1 | journal = Clin. Genet. | volume = 71 | issue = 2 | pages = 148–52 | year = 2007 | pmid = 17250663 | doi = 10.1111/j.1399-0004.2007.00739.x }}</ref> which suggests the importance of this amino acid in the overall function of TMC1. Now that TMC1 has been shown to interact with the tip link proteins PCDH15 and CDH23,<ref name="Maeda_2014"/> the next question may be whether or not amino acid 572 is necessary for TMC1 tip link interactions. | |||
}} | Researchers reported in 2015 that genetically deaf mice treated with TMC1 [[gene therapy]] recovered some of their hearing.<ref>{{cite news |last= Gallacher|first= James |date= 9 July 2015|title= Deafness could be treated by virus, say scientists|url= https://www.bbc.co.uk/news/health-33442820|publisher= BBC|location= UK|access-date= 9 July 2015}}</ref><ref>{{cite journal |last= Askew|first= Charles|date= 8 July 2015|title= Tmc gene therapy restores auditory function in deaf mice|url= |journal= Science Translational Medicine|publisher= American Association for the Advancement of Science|volume= 7|issue= 295|pages= 295ra108|doi= 10.1126/scitranslmed.aab1996|display-authors=etal|pmid=26157030}}<!--|access-date=8 July 2015--></ref> | ||
== Clinical significance == | |||
Mutations in this gene have been associated with progressive [[post-lingual deafness|postlingual hearing loss]], {{SWL|type=mutations_associated_to|target=Non-syndromic deafness|label=non syndromic deafness}}<ref>{{cite journal | vauthors = Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, Boespflug OT, Besbes G, Abdelhak S, Petit C | title = Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness | journal = PLoS ONE | volume = 9 | issue = 6 | pages = e99797 | year = 2014 | pmid = 24926664 | doi = 10.1371/journal.pone.0099797 | pmc=4057390}}</ref> and profound [[prelingual deafness]].<ref name="entrez"/> TMC1 mutations are not associated with other symptoms or abnormalities, which is known as [[Nonsyndromic hearing loss]] and indicates that TMC1 functions mainly in auditory sensation.<ref name="pmid22652773">{{cite journal | vauthors = Duman D, Tekin M | title = Autosomal recessive nonsyndromic deafness genes: a review | journal = Front Biosci | volume = 17 | issue = | pages = 2213–36 | year = 2012 | pmid = 22652773 | pmc = 3683827 | doi = 10.2741/4046}}</ref> Additionally, recessive mutations of the gene result in both a loss of TMC1 function as well as profound deafness<ref name="Kitajiri_2007"/> indicating TMC1 function is necessary for the processing of auditory signals. | |||
==References== | ==References== | ||
{{reflist| | {{reflist|35em}} | ||
==Further reading== | ==Further reading== | ||
{{refbegin | | {{refbegin|35em}} | ||
*{{cite journal | vauthors = Kitajiri SI, McNamara R, Makishima T, Husnain T, Zafar AU, Kittles RA, Ahmed ZM, Friedman TB, Riazuddin S, Griffith AJ | title = Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan. | journal = Clin. Genet. | volume = 72 | issue = 6 | pages = 546–50 | year = 2008 | pmid = 17877751 | doi = 10.1111/j.1399-0004.2007.00895.x }} | |||
*{{cite journal | vauthors = Kalay E, Karaguzel A, Caylan R, Heister A, Cremers FP, Cremers CW, Brunner HG, de Brouwer AP, Kremer H | title = Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss. | journal = Hum. Mutat. | volume = 26 | issue = 6 | pages = 591 | year = 2006 | pmid = 16287143 | doi = 10.1002/humu.9384 }} | |||
*{{cite journal | *{{cite journal | vauthors = Meyer CG, Gasmelseed NM, Mergani A, Magzoub MM, Muntau B, Thye T, Horstmann RD | title = Novel TMC1 structural and splice variants associated with congenital nonsyndromic deafness in a Sudanese pedigree. | journal = Hum. Mutat. | volume = 25 | issue = 1 | pages = 100 | year = 2006 | pmid = 15605408 | doi = 10.1002/humu.9302 }} | ||
*{{cite journal | *{{cite journal | vauthors = Keresztes G, Mutai H, Heller S | title = TMC and EVER genes belong to a larger novel family, the TMC gene family encoding transmembrane proteins. | journal = BMC Genomics | volume = 4 | pages = 24 | year = 2003 | pmid = 12812529 | pmc = 165604 | doi = 10.1186/1471-2164-4-24 }} | ||
*{{cite journal | *{{cite journal | vauthors = Scott DA, Carmi R, Elbedour K, Yosefsberg S, Stone EM, Sheffield VC | title = An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds. | journal = Am. J. Hum. Genet. | volume = 59 | issue = 2 | pages = 385–91 | year = 1996 | pmid = 8755925 | pmc = 1914732 | doi = }} | ||
*{{cite journal | *{{cite journal | vauthors = Jain PK, Fukushima K, Deshmukh D, Ramesh A, Thomas E, Lalwani AK, Kumar S, Plopis B, Skarka H, Srisailapathy CR | title = A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus. | journal = Hum. Mol. Genet. | volume = 4 | issue = 12 | pages = 2391–4 | year = 1996 | pmid = 8634715 | doi = 10.1093/hmg/4.12.2391 }} | ||
*{{cite journal | |||
*{{cite journal | |||
}} | |||
{{refend}} | {{refend}} | ||
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External IDs | GeneCards: [1] | ||||||
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Species | Human | Mouse | |||||
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Location (UCSC) | n/a | n/a | |||||
PubMed search | n/a | n/a | |||||
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Transmembrane channel-like protein 1 is a protein that in humans is encoded by the TMC1 gene.[1][2][3] TMC1 contains six transmembrane domains with both the C and N termini on the endoplasmic side of the membrane, as well as a large loop between domains 4 and 5. This topology is similar to that of transient receptor potential channels (TRPs),[1] a family of proteins involved in the perception of senses such as temperature, taste, pressure, and vision.[4] TMC1 has been located in the post-natal mouse cochlea,[1] and knockouts for TMC1 and TMC2 result in both auditory and vestibular deficits (hearing loss and balance issues) indicating TMC1 is a molecular part of auditory transduction.[5]
Function
This gene is considered a member of a gene family predicted to encode transmembrane proteins. Until recently, the specific function of this gene was relatively unknown; it was only known to be required for normal function of cochlear hair cells.[3] However, new research suggests that TMC1 interacts with Tip link proteins protocadherin 15 and cadherin 23 indicating that TMC1, along with TMC2, are necessary proteins for hair cell mechanotransduction.[6] Specifically, TMC1 and TMC2 may be two pore-forming subunits of the channel that responds to tip link deflection in hair cells.[7]
Due to its implication in cochlear hair cell function and its interaction with hair cell tip links, TMC1 is being mutated and manipulated in order to better understand the receptor while at the same time producing a molecular model for deafness. While deafness can arise at any stage of auditory processing, DFNA36 (a type of progressive hearing loss) and DFNB7/B11 (congenital hearing loss) have been specifically shown to arise from TMC1 mutations. DFNA36 results from a dominant missense mutation and DFNB7/B11 results from a recessive mutation.[1] Both have been modeled in mice, known as the Beethoven model and the dn model respectively.[2] The TMC1 gene is located on chromosome 9q31-q21, and the dominant mutation associated with DFNA36 occurs at amino acid 572[8] which suggests the importance of this amino acid in the overall function of TMC1. Now that TMC1 has been shown to interact with the tip link proteins PCDH15 and CDH23,[6] the next question may be whether or not amino acid 572 is necessary for TMC1 tip link interactions.
Researchers reported in 2015 that genetically deaf mice treated with TMC1 gene therapy recovered some of their hearing.[9][10]
Clinical significance
Mutations in this gene have been associated with progressive postlingual hearing loss, non syndromic deafness [11] and profound prelingual deafness.[3] TMC1 mutations are not associated with other symptoms or abnormalities, which is known as Nonsyndromic hearing loss and indicates that TMC1 functions mainly in auditory sensation.[12] Additionally, recessive mutations of the gene result in both a loss of TMC1 function as well as profound deafness[8] indicating TMC1 function is necessary for the processing of auditory signals.
References
- ↑ 1.0 1.1 1.2 1.3 Kurima K, Peters LM, Yang Y, Riazuddin S, Ahmed ZM, Naz S, Arnaud D, Drury S, Mo J, Makishima T, Ghosh M, Menon PS, Deshmukh D, Oddoux C, Ostrer H, Khan S, Riazuddin S, Deininger PL, Hampton LL, Sullivan SL, Battey JF, Keats BJ, Wilcox ER, Friedman TB, Griffith AJ (Mar 2002). "Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function". Nat Genet. 30 (3): 277–84. doi:10.1038/ng842. PMID 11850618.
- ↑ 2.0 2.1 Vreugde S, Erven A, Kros CJ, Marcotti W, Fuchs H, Kurima K, Wilcox ER, Friedman TB, Griffith AJ, Balling R, Hrabé De Angelis M, Avraham KB, Steel KP (2002). "Beethoven, a mouse model for dominant, progressive hearing loss DFNA36". Nat Genet. 30 (3): 257–8. doi:10.1038/ng848. PMID 11850623.
- ↑ 3.0 3.1 3.2 "Entrez Gene: TMC1 transmembrane channel-like 1".
- ↑ Vriens J, Nilius B, Voets T (2014). "Peripheral thermosensation in mammals". Nature Reviews Neuroscience. 15 (9): 573–89. doi:10.1038/nrn3784. PMID 25053448.
- ↑ Kawashima Y, Géléoc GS, Kurima K, Labay V, Lelli A, Asai Y, Makishima T, Wu DK, Della Santina CC, Holt JR, Griffith AJ (2011). "Mechanotransduction in mouse inner ear hair cells requires transmembrane channel-like genes". J. Clin. Invest. 121 (12): 4796–809. doi:10.1172/JCI60405. PMC 3223072. PMID 22105175.
- ↑ 6.0 6.1 Maeda R, Kindt KS, Mo W, Morgan CP, Erickson T, Zhao H, Clemens-Grisham R, Barr-Gillespie PG, Nicolson T (2014). "Tip-link protein protocadherin 15 interacts with transmembrane channel-like proteins TMC1 and TMC2". Proc. Natl. Acad. Sci. U.S.A. 111 (35): 12907–12. doi:10.1073/pnas.1402152111. PMC 4156717. PMID 25114259.
- ↑ Pan B, Géléoc GS, Asai Y, Horwitz GC, Kurima K, Ishikawa K, Kawashima Y, Griffith AJ, Holt JR (2013). "TMC1 and TMC2 are components of the mechanotransduction channel in hair cells of the mammalian inner ear". Neuron. 79 (3): 504–15. doi:10.1016/j.neuron.2013.06.019. PMC 3827726. PMID 23871232.
- ↑ 8.0 8.1 Kitajiri S, Makishima T, Friedman TB, Griffith AJ (2007). "A novel mutation at the DFNA36 hearing loss locus reveals a critical function and potential genotype-phenotype correlation for amino acid-572 of TMC1". Clin. Genet. 71 (2): 148–52. doi:10.1111/j.1399-0004.2007.00739.x. PMID 17250663.
- ↑ Gallacher, James (9 July 2015). "Deafness could be treated by virus, say scientists". UK: BBC. Retrieved 9 July 2015.
- ↑ Askew, Charles; et al. (8 July 2015). "Tmc gene therapy restores auditory function in deaf mice". Science Translational Medicine. American Association for the Advancement of Science. 7 (295): 295ra108. doi:10.1126/scitranslmed.aab1996. PMID 26157030.
- ↑ Riahi Z, Bonnet C, Zainine R, Louha M, Bouyacoub Y, Laroussi N, Chargui M, Kefi R, Jonard L, Dorboz I, Hardelin JP, Salah SB, Levilliers J, Weil D, McElreavey K, Boespflug OT, Besbes G, Abdelhak S, Petit C (2014). "Whole Exome Sequencing Identifies New Causative Mutations in Tunisian Families with Non-Syndromic Deafness". PLoS ONE. 9 (6): e99797. doi:10.1371/journal.pone.0099797. PMC 4057390. PMID 24926664.
- ↑ Duman D, Tekin M (2012). "Autosomal recessive nonsyndromic deafness genes: a review". Front Biosci. 17: 2213–36. doi:10.2741/4046. PMC 3683827. PMID 22652773.
Further reading
- Kitajiri SI, McNamara R, Makishima T, Husnain T, Zafar AU, Kittles RA, Ahmed ZM, Friedman TB, Riazuddin S, Griffith AJ (2008). "Identities, frequencies and origins of TMC1 mutations causing DFNB7/B11 deafness in Pakistan". Clin. Genet. 72 (6): 546–50. doi:10.1111/j.1399-0004.2007.00895.x. PMID 17877751.
- Kalay E, Karaguzel A, Caylan R, Heister A, Cremers FP, Cremers CW, Brunner HG, de Brouwer AP, Kremer H (2006). "Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss". Hum. Mutat. 26 (6): 591. doi:10.1002/humu.9384. PMID 16287143.
- Meyer CG, Gasmelseed NM, Mergani A, Magzoub MM, Muntau B, Thye T, Horstmann RD (2006). "Novel TMC1 structural and splice variants associated with congenital nonsyndromic deafness in a Sudanese pedigree". Hum. Mutat. 25 (1): 100. doi:10.1002/humu.9302. PMID 15605408.
- 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: 24. doi:10.1186/1471-2164-4-24. PMC 165604. PMID 12812529.
- Scott DA, Carmi R, Elbedour K, Yosefsberg S, Stone EM, Sheffield VC (1996). "An autosomal recessive nonsyndromic-hearing-loss locus identified by DNA pooling using two inbred Bedouin kindreds". Am. J. Hum. Genet. 59 (2): 385–91. PMC 1914732. PMID 8755925.
- Jain PK, Fukushima K, Deshmukh D, Ramesh A, Thomas E, Lalwani AK, Kumar S, Plopis B, Skarka H, Srisailapathy CR (1996). "A human recessive neurosensory nonsyndromic hearing impairment locus is potential homologue of murine deafness (dn) locus". Hum. Mol. Genet. 4 (12): 2391–4. doi:10.1093/hmg/4.12.2391. PMID 8634715.