Literature DB >> 9603735

Correction of deafness in shaker-2 mice by an unconventional myosin in a BAC transgene.

F J Probst1, R A Fridell, Y Raphael, T L Saunders, A Wang, Y Liang, R J Morell, J W Touchman, R H Lyons, K Noben-Trauth, T B Friedman, S A Camper.   

Abstract

The shaker-2 mouse mutation, the homolog of human DFNB3, causes deafness and circling behavior. A bacterial artificial chromosome (BAC) transgene from the shaker-2 critical region corrected the vestibular defects, deafness, and inner ear morphology of shaker-2 mice. An unconventional myosin gene, Myo15, was discovered by DNA sequencing of this BAC. Shaker-2 mice were found to have an amino acid substitution at a highly conserved position within the motor domain of this myosin. Auditory hair cells of shaker-2 mice have very short stereocilia and a long actin-containing protrusion extending from their basal end. This histopathology suggests that Myo15 is necessary for actin organization in the hair cells of the cochlea.

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Year:  1998        PMID: 9603735     DOI: 10.1126/science.280.5368.1444

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  118 in total

1.  A genetic approach to understanding inner ear function.

Authors:  J F Battey
Journal:  J Clin Invest       Date:  2000-12       Impact factor: 14.808

2.  ATP-Induced Ca(2+) release in cochlear outer hair cells: localization of an inositol triphosphate-gated Ca(2+) store to the base of the sensory hair bundle.

Authors:  F Mammano; G I Frolenkov; L Lagostena; I A Belyantseva; M Kurc; V Dodane; A Colavita; B Kachar
Journal:  J Neurosci       Date:  1999-08-15       Impact factor: 6.167

Review 3.  Science, medicine, and the future: New interventions in hearing impairment.

Authors:  K P Steel
Journal:  BMJ       Date:  2000-03-04

4.  A transgenic insertional inner ear mutation on mouse chromosome 1.

Authors:  R A Friedman; Y Adir; E B Crenshaw; A F Ryan; M G Rosenfeld
Journal:  Laryngoscope       Date:  2000-04       Impact factor: 3.325

Review 5.  Parallel actin bundles and their multiple actin-bundling proteins.

Authors:  J R Bartles
Journal:  Curr Opin Cell Biol       Date:  2000-02       Impact factor: 8.382

6.  ENU mutagenesis reveals a highly mutable locus on mouse Chromosome 4 that affects ear morphogenesis.

Authors:  Amy E Kiernan; Alexandra Erven; Stéphanie Voegeling; Jo Peters; Pat Nolan; Jackie Hunter; Yvonne Bacon; Karen P Steel; Steve D M Brown; Jean-Louis Guénet
Journal:  Mamm Genome       Date:  2002-03       Impact factor: 2.957

7.  Comparative maps of human 19p13.3 and mouse chromosome 10 allow identification of sequences at evolutionary breakpoints.

Authors:  R Puttagunta; L A Gordon; G E Meyer; D Kapfhamer; J E Lamerdin; P Kantheti; K M Portman; W K Chung; D E Jenne; A S Olsen; M Burmeister
Journal:  Genome Res       Date:  2000-09       Impact factor: 9.043

8.  Human nonsyndromic hereditary deafness DFNA17 is due to a mutation in nonmuscle myosin MYH9.

Authors:  A K Lalwani; J A Goldstein; M J Kelley; W Luxford; C M Castelein; A N Mhatre
Journal:  Am J Hum Genet       Date:  2000-10-09       Impact factor: 11.025

9.  The circling behavior of the deafblind LEW-ci2 rat is linked to a segment of RNO10 containing Myo15 and Kcnj12.

Authors:  Wojciech T Chwalisz; Bernd U Koelsch; Andrea Kindler-Röhrborn; Hans J Hedrich; Dirk Wedekind
Journal:  Mamm Genome       Date:  2003-09       Impact factor: 2.957

10.  Therapy of hearing disorders - conservative procedures.

Authors:  Stefan Plontke
Journal:  GMS Curr Top Otorhinolaryngol Head Neck Surg       Date:  2005-09-28
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