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Identifying components of the hair-cell interactome involved in cochlear amplification

BACKGROUND: Although outer hair cells (OHCs) play a key role in cochlear amplification, it is not fully understood how they amplify sound signals by more than 100 fold. Two competing or possibly complementary mechanisms, stereocilia-based and somatic electromotility-based amplification, have been co...

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Autores principales: Zheng, Jing, Anderson, Charles T, Miller, Katharine K, Cheatham, MaryAnn, Dallos, Peter
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669096/
https://www.ncbi.nlm.nih.gov/pubmed/19320974
http://dx.doi.org/10.1186/1471-2164-10-127
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author Zheng, Jing
Anderson, Charles T
Miller, Katharine K
Cheatham, MaryAnn
Dallos, Peter
author_facet Zheng, Jing
Anderson, Charles T
Miller, Katharine K
Cheatham, MaryAnn
Dallos, Peter
author_sort Zheng, Jing
collection PubMed
description BACKGROUND: Although outer hair cells (OHCs) play a key role in cochlear amplification, it is not fully understood how they amplify sound signals by more than 100 fold. Two competing or possibly complementary mechanisms, stereocilia-based and somatic electromotility-based amplification, have been considered. Lacking knowledge about the exceptionally rich protein networks in the OHC plasma membrane, as well as related protein-protein interactions, limits our understanding of cochlear function. Therefore, we focused on finding protein partners for two important membrane proteins: Cadherin 23 (cdh23) and prestin. Cdh23 is one of the tip-link proteins involved in transducer function, a key component of mechanoelectrical transduction and stereocilia-based amplification. Prestin is a basolateral membrane protein responsible for OHC somatic electromotility. RESULTS: Using the membrane-based yeast two-hybrid system to screen a newly built cDNA library made predominantly from OHCs, we identified two completely different groups of potential protein partners using prestin and cdh23 as bait. These include both membrane bound and cytoplasmic proteins with 12 being de novo gene products with unknown function(s). In addition, some of these genes are closely associated with deafness loci, implying a potentially important role in hearing. The most abundant prey for prestin (38%) is composed of a group of proteins involved in electron transport, which may play a role in OHC survival. The most abundant group of cdh23 prey (55%) contains calcium-binding domains. Since calcium performs an important role in hair cell mechanoelectrical transduction and amplification, understanding the interactions between cdh23 and calcium-binding proteins should increase our knowledge of hair cell function at the molecular level. CONCLUSION: The results of this study shed light on some protein networks in cochlear hair cells. Not only was a group of de novo genes closely associated with known deafness loci identified, but the data also indicate that the hair cell tip link interacts directly with calcium binding proteins. The OHC motor protein, prestin, also appears to be associated with electron transport proteins. These unanticipated results open potentially fruitful lines of investigation into the molecular basis of cochlear amplification.
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spelling pubmed-26690962009-04-15 Identifying components of the hair-cell interactome involved in cochlear amplification Zheng, Jing Anderson, Charles T Miller, Katharine K Cheatham, MaryAnn Dallos, Peter BMC Genomics Research Article BACKGROUND: Although outer hair cells (OHCs) play a key role in cochlear amplification, it is not fully understood how they amplify sound signals by more than 100 fold. Two competing or possibly complementary mechanisms, stereocilia-based and somatic electromotility-based amplification, have been considered. Lacking knowledge about the exceptionally rich protein networks in the OHC plasma membrane, as well as related protein-protein interactions, limits our understanding of cochlear function. Therefore, we focused on finding protein partners for two important membrane proteins: Cadherin 23 (cdh23) and prestin. Cdh23 is one of the tip-link proteins involved in transducer function, a key component of mechanoelectrical transduction and stereocilia-based amplification. Prestin is a basolateral membrane protein responsible for OHC somatic electromotility. RESULTS: Using the membrane-based yeast two-hybrid system to screen a newly built cDNA library made predominantly from OHCs, we identified two completely different groups of potential protein partners using prestin and cdh23 as bait. These include both membrane bound and cytoplasmic proteins with 12 being de novo gene products with unknown function(s). In addition, some of these genes are closely associated with deafness loci, implying a potentially important role in hearing. The most abundant prey for prestin (38%) is composed of a group of proteins involved in electron transport, which may play a role in OHC survival. The most abundant group of cdh23 prey (55%) contains calcium-binding domains. Since calcium performs an important role in hair cell mechanoelectrical transduction and amplification, understanding the interactions between cdh23 and calcium-binding proteins should increase our knowledge of hair cell function at the molecular level. CONCLUSION: The results of this study shed light on some protein networks in cochlear hair cells. Not only was a group of de novo genes closely associated with known deafness loci identified, but the data also indicate that the hair cell tip link interacts directly with calcium binding proteins. The OHC motor protein, prestin, also appears to be associated with electron transport proteins. These unanticipated results open potentially fruitful lines of investigation into the molecular basis of cochlear amplification. BioMed Central 2009-03-25 /pmc/articles/PMC2669096/ /pubmed/19320974 http://dx.doi.org/10.1186/1471-2164-10-127 Text en Copyright © 2009 Zheng et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Zheng, Jing
Anderson, Charles T
Miller, Katharine K
Cheatham, MaryAnn
Dallos, Peter
Identifying components of the hair-cell interactome involved in cochlear amplification
title Identifying components of the hair-cell interactome involved in cochlear amplification
title_full Identifying components of the hair-cell interactome involved in cochlear amplification
title_fullStr Identifying components of the hair-cell interactome involved in cochlear amplification
title_full_unstemmed Identifying components of the hair-cell interactome involved in cochlear amplification
title_short Identifying components of the hair-cell interactome involved in cochlear amplification
title_sort identifying components of the hair-cell interactome involved in cochlear amplification
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2669096/
https://www.ncbi.nlm.nih.gov/pubmed/19320974
http://dx.doi.org/10.1186/1471-2164-10-127
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