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Novel COCH p.V123E Mutation, Causative of DFNA9 Sensorineural Hearing Loss and Vestibular Disorder, Shows Impaired Cochlin Post-Translational Cleavage and Secretion

Authors
 Jinsei Jung  ;  Han Sang Kim  ;  Min Goo Lee  ;  Eun Jin Yang  ;  Jae Young Choi 
Citation
 HUMAN MUTATION, Vol.36(12) : 1168-1175, 2015 
Journal Title
 HUMAN MUTATION 
ISSN
 1059-7794 
Issue Date
2015
MeSH
Adult ; Amino Acid Sequence ; Amino Acid Substitution* ; Cell Line ; Codon* ; Extracellular Matrix Proteins/chemistry ; Extracellular Matrix Proteins/genetics* ; Extracellular Matrix Proteins/metabolism ; Genes, Dominant ; Hearing Loss, Sensorineural/diagnosis ; Hearing Loss, Sensorineural/genetics* ; Hearing Loss, Sensorineural/metabolism ; Hearing Tests ; High-Throughput Nucleotide Sequencing ; Humans ; Magnetic Resonance Imaging ; Middle Aged ; Mutation* ; Pedigree ; Protein Multimerization ; Protein Processing, Post-Translational ; Protein Transport ; Proteolysis ; Tomography, X-Ray Computed ; Vestibular Diseases/diagnosis ; Vestibular Diseases/genetics* ; Vestibular Diseases/metabolism
Keywords
DFNA9 ; hearing loss ; cochlin ; post-translational cleavage ; aggrecanase
Abstract
DFNA9 is an autosomal dominant disorder characterized by late-onset, non-syndromic hearing loss, and vestibular dysfunction. Mutations in the COCH (coagulation factor C homology) gene encoding cochlin are etiologically linked to DFNA9. Previous studies have shown that cochlin is cleaved by aggrecanase-1 during inflammation in the spleen and that the cleaved LCCL domain functions as an innate immune mediator. However, the physiological role of cochlin in the inner ear is not completely understood. Here, we report that cochlins containing DFNA9-linked mutations (p.P51S, p.V66G, p.G88E, p.I109T, p.W117R, p.V123E, and p.C162Y) demonstrate reduced cleavage by aggrecanase. Notably, in families affected with DFNA9, we found a novel COCH mutation causing p.V123E substitution in cochlin, which significantly reduced protein susceptibility to cleavage by aggrecanase (to about 20.5% of the wild-type). These results suggest that the impaired post-translational cleavage of cochlin mutants may be associated with pathological mechanisms underlying DFNA9-related sensorineural hearing loss.
Full Text
http://onlinelibrary.wiley.com/doi/10.1002/humu.22855/abstract
DOI
10.1002/humu.22855
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Pharmacology (약리학교실) > 1. Journal Papers
1. College of Medicine (의과대학) > Dept. of Otorhinolaryngology (이비인후과학교실) > 1. Journal Papers
Yonsei Authors
Kim, Han Sang(김한상) ORCID logo https://orcid.org/0000-0002-6504-9927
Lee, Min Goo(이민구) ORCID logo https://orcid.org/0000-0001-7436-012X
Jung, Jinsei(정진세) ORCID logo https://orcid.org/0000-0003-1906-6969
Choi, Jae Young(최재영) ORCID logo https://orcid.org/0000-0001-9493-3458
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/156828
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