Literature DB >> 21368133

Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).

Jing Zheng1, Katharine K Miller, Tao Yang, Michael S Hildebrand, A Eliot Shearer, Adam P DeLuca, Todd E Scheetz, Jennifer Drummond, Steve E Scherer, P Kevin Legan, Richard J Goodyear, Guy P Richardson, Mary Ann Cheatham, Richard J Smith, Peter Dallos.   

Abstract

We report on a secreted protein found in mammalian cochlear outer hair cells (OHC) that is a member of the carcinoembryonic antigen-related cell adhesion molecule (CEACAM) family of adhesion proteins. Ceacam16 mRNA is expressed in OHC, and its protein product localizes to the tips of the tallest stereocilia and the tectorial membrane (TM). This specific localization suggests a role in maintaining the integrity of the TM as well as in the connection between the OHC stereocilia and TM, a linkage essential for mechanical amplification. In agreement with this role, CEACAM16 colocalizes and coimmunoprecipitates with the TM protein α-tectorin. In addition, we show that mutation of CEACAM16 leads to autosomal dominant nonsyndromic deafness (ADNSHL) at the autosomal dominant hearing loss (DFNA4) locus. In aggregate, these data identify CEACAM16 as an α-tectorin-interacting protein that concentrates at the point of attachment of the TM to the stereocilia and, when mutated, results in ADNSHL at the DFNA4 locus.

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Year:  2011        PMID: 21368133      PMCID: PMC3054008          DOI: 10.1073/pnas.1005842108

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  36 in total

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3.  Role of the tectorial membrane revealed by otoacoustic emissions recorded from wild-type and transgenic Tecta(deltaENT/deltaENT) mice.

Authors:  Andrei N Lukashkin; Victoria A Lukashkina; P Kevin Legan; Guy P Richardson; Ian J Russell
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4.  Exosomes bearing HLA-DR1 molecules need dendritic cells to efficiently stimulate specific T cells.

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Journal:  Int Immunol       Date:  2002-07       Impact factor: 4.823

5.  Glycosylation affects rat Kv1.1 potassium channel gating by a combined surface potential and cooperative subunit interaction mechanism.

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Review 6.  Intracellular functions of N-linked glycans.

Authors:  A Helenius; M Aebi
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7.  A targeted deletion in alpha-tectorin reveals that the tectorial membrane is required for the gain and timing of cochlear feedback.

Authors:  P K Legan; V A Lukashkina; R J Goodyear; M Kössi; I J Russell; G P Richardson
Journal:  Neuron       Date:  2000-10       Impact factor: 17.173

8.  Structure of outer hair cell stereocilia side and attachment links in the chinchilla cochlea.

Authors:  Vladimir Tsuprun; Peter Santi
Journal:  J Histochem Cytochem       Date:  2002-04       Impact factor: 2.479

9.  Evidence for multiple, developmentally regulated isoforms of Ptprq on hair cells of the inner ear.

Authors:  Gowri Nayak; Richard J Goodyear; P Kevin Legan; Masaharu Noda; Guy P Richardson
Journal:  Dev Neurobiol       Date:  2011-02       Impact factor: 3.964

10.  Nonmuscle myosin heavy-chain gene MYH14 is expressed in cochlea and mutated in patients affected by autosomal dominant hearing impairment (DFNA4).

Authors:  Francesca Donaudy; Rik Snoeckx; Markus Pfister; Hans-Peter Zenner; Nikolaus Blin; Mariateresa Di Stazio; Antonella Ferrara; Carmen Lanzara; Romina Ficarella; Frank Declau; Carsten M Pusch; Peter Nürnberg; Salvatore Melchionda; Leopoldo Zelante; Ester Ballana; Xavier Estivill; Guy Van Camp; Paolo Gasparini; Anna Savoia
Journal:  Am J Hum Genet       Date:  2004-03-10       Impact factor: 11.025

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  55 in total

1.  Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans.

Authors:  Alex Marcel Moreira Dias; Karina Lezirovitz; Fernanda Stávale Nicastro; Beatriz C A Mendes; Regina Célia Mingroni-Netto
Journal:  J Hum Genet       Date:  2018-12-04       Impact factor: 3.172

Review 2.  Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities.

Authors:  Xi Lin; Wenxue Tang; Shoeb Ahmad; Jingqiao Lu; Candice C Colby; Jason Zhu; Qing Yu
Journal:  Hear Res       Date:  2012-01-14       Impact factor: 3.208

3.  Diverse oligomeric states of CEACAM IgV domains.

Authors:  Daniel A Bonsor; Sebastian Günther; Robert Beadenkopf; Dorothy Beckett; Eric J Sundberg
Journal:  Proc Natl Acad Sci U S A       Date:  2015-10-19       Impact factor: 11.205

Review 4.  Deafness in the genomics era.

Authors:  A Eliot Shearer; Michael S Hildebrand; Christina M Sloan; Richard J H Smith
Journal:  Hear Res       Date:  2011-10-08       Impact factor: 3.208

5.  Clarification of glycosylphosphatidylinositol anchorage of OTOANCORIN and human OTOA variants associated with deafness.

Authors:  Bong Jik Kim; Dong-Kyu Kim; Jin Hee Han; Jayoung Oh; Ah Reum Kim; Chung Lee; Nayoung Kd Kim; Hye-Rim Park; Min Young Kim; Sejoon Lee; Seungmin Lee; Doo Yi Oh; Woong-Yang Park; Sungjin Park; Byung Yoon Choi
Journal:  Hum Mutat       Date:  2019-02-28       Impact factor: 4.878

Review 6.  Congenital hearing loss.

Authors:  Anna M H Korver; Richard J H Smith; Guy Van Camp; Mark R Schleiss; Maria A K Bitner-Glindzicz; Lawrence R Lustig; Shin-Ichi Usami; An N Boudewyns
Journal:  Nat Rev Dis Primers       Date:  2017-01-12       Impact factor: 52.329

Review 7.  Whole-exome sequencing and its impact in hereditary hearing loss.

Authors:  Tahir Atik; Guney Bademci; Oscar Diaz-Horta; Susan H Blanton; Mustafa Tekin
Journal:  Genet Res (Camb)       Date:  2015-03-31       Impact factor: 1.588

8.  Clue to a new deafness gene: a large Chinese nonsyndromic hearing loss family linked to DFNA4.

Authors:  Liang Zong; Chunye Lu; Yali Zhao; Qian Li; Dongyi Han; Weiyan Yang; Yan Shen; Qingyin Zheng; Qiuju Wang
Journal:  J Genet Genomics       Date:  2012-11-16       Impact factor: 4.275

Review 9.  Genetics: advances in genetic testing for deafness.

Authors:  A Eliot Shearer; Richard J H Smith
Journal:  Curr Opin Pediatr       Date:  2012-12       Impact factor: 2.856

10.  Loss of the tectorial membrane protein CEACAM16 enhances spontaneous, stimulus-frequency, and transiently evoked otoacoustic emissions.

Authors:  Mary Ann Cheatham; Richard J Goodyear; Kazuaki Homma; P Kevin Legan; Julia Korchagina; Souvik Naskar; Jonathan H Siegel; Peter Dallos; Jing Zheng; Guy P Richardson
Journal:  J Neurosci       Date:  2014-07-30       Impact factor: 6.167

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