Literature DB >> 12485990

Myosin VIIa, harmonin and cadherin 23, three Usher I gene products that cooperate to shape the sensory hair cell bundle.

Batiste Boëda1, Aziz El-Amraoui, Amel Bahloul, Richard Goodyear, Laurent Daviet, Stéphane Blanchard, Isabelle Perfettini, Karl R Fath, Spencer Shorte, Jan Reiners, Anne Houdusse, Pierre Legrain, Uwe Wolfrum, Guy Richardson, Christine Petit.   

Abstract

Deaf-blindness in three distinct genetic forms of Usher type I syndrome (USH1) is caused by defects in myosin VIIa, harmonin and cadherin 23. Despite being critical for hearing, the functions of these proteins in the inner ear remain elusive. Here we show that harmonin, a PDZ domain-containing protein, and cadherin 23 are both present in the growing stereocilia and that they bind to each other. Moreover, we demonstrate that harmonin b is an F-actin-bundling protein, which is thus likely to anchor cadherin 23 to the stereocilia microfilaments, thereby identifying a novel anchorage mode of the cadherins to the actin cytoskeleton. Moreover, harmonin b interacts directly with myosin VIIa, and is absent from the disorganized hair bundles of myosin VIIa mutant mice, suggesting that myosin VIIa conveys harmonin b along the actin core of the developing stereocilia. We propose that the shaping of the hair bundle relies on a functional unit composed of myosin VIIa, harmonin b and cadherin 23 that is essential to ensure the cohesion of the stereocilia.

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Year:  2002        PMID: 12485990      PMCID: PMC139109          DOI: 10.1093/emboj/cdf689

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  44 in total

1.  Establishment of hair bundle polarity and orientation in the developing vestibular system of the mouse.

Authors:  K Denman-Johnson; A Forge
Journal:  J Neurocytol       Date:  1999 Oct-Nov

2.  Cloning and expression throughout mouse development of mfat1, a homologue of the Drosophila tumour suppressor gene fat.

Authors:  B Cox; A K Hadjantonakis; J E Collins; A I Magee
Journal:  Dev Dyn       Date:  2000-03       Impact factor: 3.780

3.  Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D.

Authors:  F Di Palma; R H Holme; E C Bryda; I A Belyantseva; R Pellegrino; B Kachar; K P Steel; K Noben-Trauth
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

4.  The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene.

Authors:  K N Alagramam; C L Murcia; H Y Kwon; K S Pawlowski; C G Wright; R P Woychik
Journal:  Nat Genet       Date:  2001-01       Impact factor: 38.330

5.  A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.

Authors:  M Bitner-Glindzicz; K J Lindley; P Rutland; D Blaydon; V V Smith; P J Milla; K Hussain; J Furth-Lavi; K E Cosgrove; R M Shepherd; P D Barnes; R E O'Brien; P A Farndon; J Sowden; X Z Liu; M J Scanlan; S Malcolm; M J Dunne; A Aynsley-Green; B Glaser
Journal:  Nat Genet       Date:  2000-09       Impact factor: 38.330

6.  A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.

Authors:  E Verpy; M Leibovici; I Zwaenepoel; X Z Liu; A Gal; N Salem; A Mansour; S Blanchard; I Kobayashi; B J Keats; R Slim; C Petit
Journal:  Nat Genet       Date:  2000-09       Impact factor: 38.330

7.  The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins.

Authors:  L Zheng; G Sekerková; K Vranich; L G Tilney; E Mugnaini; J R Bartles
Journal:  Cell       Date:  2000-08-04       Impact factor: 41.582

8.  Vezatin, a novel transmembrane protein, bridges myosin VIIA to the cadherin-catenins complex.

Authors:  P Küssel-Andermann; A El-Amraoui; S Safieddine; S Nouaille; I Perfettini; M Lecuit; P Cossart; U Wolfrum; C Petit
Journal:  EMBO J       Date:  2000-11-15       Impact factor: 11.598

Review 9.  F-actin bundles are derivatives of microvilli: What does this tell us about how bundles might form?

Authors:  D J DeRosier; L G Tilney
Journal:  J Cell Biol       Date:  2000-01-10       Impact factor: 10.539

10.  Components of cell-matrix adhesions.

Authors:  E Zamir; B Geiger
Journal:  J Cell Sci       Date:  2001-10       Impact factor: 5.285

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  178 in total

Review 1.  Coupling adhesion to actin bundles in the inner ear. Novel functions for novel cadherins.

Authors:  Astrid Kraemer; Alpha S Yap
Journal:  EMBO Rep       Date:  2003-03       Impact factor: 8.807

Review 2.  Keeping sensory cells and evolving neurons to connect them to the brain: molecular conservation and novelties in vertebrate ear development.

Authors:  B Fritzsch; K W Beisel
Journal:  Brain Behav Evol       Date:  2004       Impact factor: 1.808

3.  Coupling of the mechanotransduction machinery and F-actin polymerization in the cochlear hair bundles.

Authors:  Elisa Caberlotto; Vincent Michel; Jacques Boutet de Monvel; Christine Petit
Journal:  Bioarchitecture       Date:  2011-07-01

Review 4.  Genetics and pathological mechanisms of Usher syndrome.

Authors:  Denise Yan; Xue Z Liu
Journal:  J Hum Genet       Date:  2010-04-09       Impact factor: 3.172

5.  Zooming in on Cadherin-23: Structural Diversity and Potential Mechanisms of Inherited Deafness.

Authors:  Avinash Jaiganesh; Pedro De-la-Torre; Aniket A Patel; Domenic J Termine; Florencia Velez-Cortes; Conghui Chen; Marcos Sotomayor
Journal:  Structure       Date:  2018-07-19       Impact factor: 5.006

6.  Regulated vesicular trafficking of specific PCDH15 and VLGR1 variants in auditory hair cells.

Authors:  Marisa Zallocchi; Duane Delimont; Daniel T Meehan; Dominic Cosgrove
Journal:  J Neurosci       Date:  2012-10-03       Impact factor: 6.167

7.  A mutation in the gamma actin 1 (ACTG1) gene causes autosomal dominant hearing loss (DFNA20/26).

Authors:  E van Wijk; E Krieger; M H Kemperman; E M R De Leenheer; P L M Huygen; C W R J Cremers; F P M Cremers; H Kremer
Journal:  J Med Genet       Date:  2003-12       Impact factor: 6.318

8.  Cyclic nucleotide-gated channel α-3 (CNGA3) interacts with stereocilia tip-link cadherin 23 + exon 68 or alternatively with myosin VIIa, two proteins required for hair cell mechanotransduction.

Authors:  Dakshnamurthy Selvakumar; Marian J Drescher; Dennis G Drescher
Journal:  J Biol Chem       Date:  2013-01-17       Impact factor: 5.157

9.  Role of myosin VIIa and Rab27a in the motility and localization of RPE melanosomes.

Authors:  Daniel Gibbs; Sassan M Azarian; Concepcion Lillo; Junko Kitamoto; Adriana E Klomp; Karen P Steel; Richard T Libby; David S Williams
Journal:  J Cell Sci       Date:  2004-11-30       Impact factor: 5.285

10.  Targeted knockout and lacZ reporter expression of the mouse Tmhs deafness gene and characterization of the hscy-2J mutation.

Authors:  Chantal M Longo-Guess; Leona H Gagnon; Bernd Fritzsch; Kenneth R Johnson
Journal:  Mamm Genome       Date:  2007-09-18       Impact factor: 2.957

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