Literature DB >> 10471988

Myosins and deafness.

M J Redowicz1.   

Abstract

The discovery in the past few years of a huge diversity within the myosin superfamily has been coupled with an understanding of the role of these motor proteins in various cellular functions. Extensive studies have revealed that myosin isoforms are not only involved in muscle contraction but also in crucial functions of many specialized mammalian cells such as melanocytes, kidney and intestinal brush border microvilli, nerve growth cones or inner ear hair cells. A search for genes involved in the pathology of human genetic deafness resulted in identification of three novel myosins: myosin VI, myosin VIIA and, very recently, myosin XV. The structure, tissue and cellular distribution of these myosin isoforms, as well as mutations detected within their genes that have been found to affect the hearing process, are described in this review.

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Year:  1999        PMID: 10471988     DOI: 10.1023/a:1005403725521

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  38 in total

1.  Autosomal dominant non-syndromic deafness caused by a mutation in the myosin VIIA gene.

Authors:  X Z Liu; J Walsh; Y Tamagawa; K Kitamura; M Nishizawa; K P Steel; S D Brown
Journal:  Nat Genet       Date:  1997-11       Impact factor: 38.330

Review 2.  Unconventional myosins in cell movement, membrane traffic, and signal transduction.

Authors:  V Mermall; P L Post; M S Mooseker
Journal:  Science       Date:  1998-01-23       Impact factor: 47.728

3.  Mutations in the myosin VIIA gene cause non-syndromic recessive deafness.

Authors:  X Z Liu; J Walsh; P Mburu; J Kendrick-Jones; M J Cope; K P Steel; S D Brown
Journal:  Nat Genet       Date:  1997-06       Impact factor: 38.330

4.  Mutation in transcription factor POU4F3 associated with inherited progressive hearing loss in humans.

Authors:  O Vahava; R Morell; E D Lynch; S Weiss; M E Kagan; N Ahituv; J E Morrow; M K Lee; A B Skvorak; C C Morton; A Blumenfeld; M Frydman; T B Friedman; M C King; K B Avraham
Journal:  Science       Date:  1998-03-20       Impact factor: 47.728

5.  Unconventional myosins in inner-ear sensory epithelia.

Authors:  T Hasson; P G Gillespie; J A Garcia; R B MacDonald; Y Zhao; A G Yee; M S Mooseker; D P Corey
Journal:  J Cell Biol       Date:  1997-06-16       Impact factor: 10.539

6.  Defective myosin VIIA gene responsible for Usher syndrome type 1B.

Authors:  D Weil; S Blanchard; J Kaplan; P Guilford; F Gibson; J Walsh; P Mburu; A Varela; J Levilliers; M D Weston
Journal:  Nature       Date:  1995-03-02       Impact factor: 49.962

7.  Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.

Authors:  J D Eudy; M D Weston; S Yao; D M Hoover; H L Rehm; M Ma-Edmonds; D Yan; I Ahmad; J J Cheng; C Ayuso; C Cremers; S Davenport; C Moller; C B Talmadge; K W Beisel; M Tamayo; C C Morton; A Swaroop; W J Kimberling; J Sumegi
Journal:  Science       Date:  1998-06-12       Impact factor: 47.728

8.  Shaker-1 mutations reveal roles for myosin VIIA in both development and function of cochlear hair cells.

Authors:  T Self; M Mahony; J Fleming; J Walsh; S D Brown; K P Steel
Journal:  Development       Date:  1998-02       Impact factor: 6.868

9.  Myosin V associates with melanosomes in mouse melanocytes: evidence that myosin V is an organelle motor.

Authors:  X Wu; B Bowers; Q Wei; B Kocher; J A Hammer
Journal:  J Cell Sci       Date:  1997-04       Impact factor: 5.285

10.  Functional studies of the domains of talin.

Authors:  G H Nuckolls; C E Turner; K Burridge
Journal:  J Cell Biol       Date:  1990-05       Impact factor: 10.539

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  13 in total

1.  Myo3A, one of two class III myosin genes expressed in vertebrate retina, is localized to the calycal processes of rod and cone photoreceptors and is expressed in the sacculus.

Authors:  Andréa C Dosé; David W Hillman; Cynthia Wong; Lorraine Sohlberg; Jennifer Lin-Jones; Beth Burnside
Journal:  Mol Biol Cell       Date:  2003-03       Impact factor: 4.138

2.  Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.

Authors:  Zohreh Fattahi; A Eliot Shearer; Mojgan Babanejad; Niloofar Bazazzadegan; Seyed Navid Almadani; Nooshin Nikzat; Khadijeh Jalalvand; Sanaz Arzhangi; Fatemehsadat Esteghamat; Rezvan Abtahi; Batool Azadeh; Richard J H Smith; Kimia Kahrizi; Hossein Najmabadi
Journal:  Am J Med Genet A       Date:  2012-06-26       Impact factor: 2.802

3.  Whole genome expression in peripheral-blood samples of workers professionally exposed to polycyclic aromatic hydrocarbons.

Authors:  Ming-Tsang Wu; Tzu-Chi Lee; I-Chen Wu; Hung-Ju Su; Jie-Len Huang; Chiung-Yu Peng; Weihsin Wang; Ting-Yu Chou; Ming-Yen Lin; Wen-Yi Lin; Chia-Tsuan Huang; Chih-Hong Pan; Chi-Kung Ho
Journal:  Chem Res Toxicol       Date:  2011-09-02       Impact factor: 3.739

Review 4.  Regulation of nonmuscle myosins by heavy chain phosphorylation.

Authors:  M J Redowicz
Journal:  J Muscle Res Cell Motil       Date:  2001       Impact factor: 2.698

5.  Myosin XVA expression in the pituitary and in other neuroendocrine tissues and tumors.

Authors:  R V Lloyd; S Vidal; L Jin; S Zhang; K Kovacs; E Horvath; B W Scheithauer; E T Boger; R A Fridell; T B Friedman
Journal:  Am J Pathol       Date:  2001-10       Impact factor: 4.307

Review 6.  Myosin motor function: the ins and outs of actin-based membrane protrusions.

Authors:  Rajalakshmi Nambiar; Russell E McConnell; Matthew J Tyska
Journal:  Cell Mol Life Sci       Date:  2010-01-27       Impact factor: 9.261

7.  Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss.

Authors:  Fengguo Zhang; Lei Xu; Yun Xiao; Jianfeng Li; Xiaohui Bai; Haibo Wang
Journal:  Neural Plast       Date:  2018-04-05       Impact factor: 3.599

8.  Genotype-phenotype correlation analysis of MYO15A variants in autosomal recessive non-syndromic hearing loss.

Authors:  Jing Zhang; Jing Guan; Hongyang Wang; Linwei Yin; Dayong Wang; Lidong Zhao; Huifang Zhou; Qiuju Wang
Journal:  BMC Med Genet       Date:  2019-04-05       Impact factor: 2.103

9.  Structural basis of Fusarium myosin I inhibition by phenamacril.

Authors:  Yuxin Zhou; X Edward Zhou; Yuanping Gong; Yuanye Zhu; Xiaoman Cao; Joseph S Brunzelle; H Eric Xu; Mingguo Zhou; Karsten Melcher; Feng Zhang
Journal:  PLoS Pathog       Date:  2020-03-12       Impact factor: 6.823

10.  Whole-exome sequencing identifies MYO15A mutations as a cause of autosomal recessive nonsyndromic hearing loss in Korean families.

Authors:  Hae-Mi Woo; Hong-Joon Park; Jeong-In Baek; Mi-Hyun Park; Un-Kyung Kim; Borum Sagong; Soo Kyung Koo
Journal:  BMC Med Genet       Date:  2013-07-17       Impact factor: 2.103

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