Unconventional myosins, the basis for deafness in mouse and man

American Journal of Human Genetics

Volumn 61, Issue 4, 1997, Pages 801-805

  Hasson, T ^a  

^a YALE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CALCIUM BINDING PROTEIN; MYOSIN;

ACTIN FILAMENT; EDITORIAL; GENE MUTATION; HEARING IMPAIRMENT; HUMAN; HYDROLYSIS; INNER EAR MALFORMATION; MOUSE; NONHUMAN; PHYLOGENY; PRIORITY JOURNAL; PROTEIN ANALYSIS;

EID: 0030846814     PISSN: 00029297     EISSN: None     Source Type: Journal    
DOI: 10.1086/514890     Document Type: Editorial

References (27)

1. A Adato D Weil H Kalinski Y Pel-Or A Hammadi C Petit M Korostishevsky Mutation profile of all 49 exons of the human myosin VIIA gene, and haplotype analysis, of Usher IB families from diverse origins Am J Hum Genet 61 1997 813 821 (in this issue)
2. KB Avraham T Hasson T Sobe B Balsara JR Testa B Skvorak CC Morton Characterization of unconventional MYO6 , the human homologue of the gene responsible for deafness in Snell's waltzer mice Hum Mol Genet 6 1997 1225 1231
3. KB Avraham T Hasson KP Steel DM Kingsley LB Russell MS Mooseker NG Copeland The mouse Snell's waltzer deafness gene encodes an unconventional myosin required for structural integrity of inner hair cells Nat Genet 11 1995 369 374
4. KA Brown MJ Sutcliffe KP Steel SDM Brown Close linkage of the olfactory marker protein gene to the mouse deafness mutation shaker-1 Genomics 13 1992 189 193
5. Z-Y Chen T Hasson PM Kelley BJ Schwender MF Schwartz M Ramakrishnan WJ Kimberling Molecular cloning and domain structure of human myosin-VIIa, the gene product defective in Usher syndrome 1B Genomics 36 1996 440 448
6. F Crozet A El-Amraoui S Blanchard M Lenoir C Ripoll P Vago C Hamel Cloning of the genes encoding two murine and human cochlear unconventional type I myosins Genomics 40 1997 332 341
7. A El-Amraoui I Sahly S Picaud J Sahel M Abitbol C Petit Human Usher 1B/mouse shaker-1: the retinal pheno-type discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells Hum Mol Genet 5 1996 1171 1178
8. F Gibson J Walsh P Mburu A Varela KA Brown M Antonio K Beisel The shaker-1 mouse deafness mutation encodes a myosin-VII motor Nature 374 1995 62 64
9. PG Gillespie T Hasson JA Garcia DP Corey Multiple myosin isozymes and hair-cell function Cold Spring Harb Symp Quant Biol 61 1996 309 318
10. T Hasson PG Gillespie JA Garcia RB MacDonald Y-D Zhao AG Yee MS Mooseker Unconventional myosins in inner-ear sensory epithelia J Cell Biol 137 1997 a 1287 1307
11. T Hasson MB Heintzelman J Santos-Sacchi DP Corey MS Mooseker Expression in cochlea and retina of myosin VIIa, the gene product defective in Usher syndrome type 1B Proc Natl Acad Sci USA 92 1995 9815 9819
12. T Hasson MS Mooseker Vertebrate unconventional myosins J Biol Chem 271 1996 16431 16434
13. T Hasson JF Skowron DJ Gilbert KB Avraham WL Perry WM Bement BL Anderson Mapping of unconventional myosins in mouse and human Genomics 36 1996 431 439
14. T Hasson J Walsh J Cable MS Mooseker SDM Brown KP Steel Effects of shaker-1 mutations on myosin-VIIa protein and mRNA expression Cell Motil Cytoskel 37 1997 b 127 138
15. G Levy F Levi-Acobas S Blanchard S Gerber D Larget-Piet V Chenal X-Z Liu Myosin VIIa gene: heterogeneity of mutations responsible for Usher syndrome type 1B Hum Mol Genet 6 1997 111 116
16. X Liu G Vansant IP Udovichenko U Wolfrum DS Williams Myosin VIIa, the product of the Usher 1B syndrome gene, is concentrated in the connecting cilia of photoreceptor cells Cell Motil Cytoskel 37 1997 a 240 252
17. X-Z Liu J Walsh P Mburu J Kendrick-Jones MJTV Cope KP Steel SDM Brown Mutations in the myosin-VIIa gene cause non-syndromic recessive deafness Nat Genet 16 1997 b 188 190
18. MS Mooseker RE Cheney Unconventional myosins Annu Rev Cell Dev Biol 11 1995 633 675
19. I Rayment WR Rypniewski K Schmidt-Base R Smith DR Tomchick MM Benning DA Winkelman Three-dimensional structure of myosin subfragment-1: a molecular motor Science 261 1993 50 58
20. Y Tamagawa K Kitamura T Ishida K Ishikawa H Tanaka S Tsuji M Nishizawa A gene for a dominant form of non-syndromic sensorineural deafness ( DFNA11 ) maps within the region containing DFNB2 recessive deafness gene Hum Mol Genet 5 1996 849 852
21. TQP Uyeda PD Abramson JA Spudich The neck region of the myosin motor domain acts as a lever arm to generate movement Proc Natl Acad Sci USA 93 1996 4459 4464
22. G Van Camp PJ Willems RJH Smith Nonsyndromic hearing impairment: unparalleled heterogeneity Am J Hum Genet 60 1997 758 764
23. KL Vikstrom LA Leinwand Contractile protein mutations and heat disease Curr Opin Cell Biol 8 1996 97 105
24. D Weil S Blanchard J Kaplan P Guilford F Gibson J Walsh P Mburu Defective myosin-VIIA gene responsible for Usher syndrome type 1B Nature 374 1995 60 61
25. D Weil P Kussel S Blanchard G Levy F Levi-Acobas M Drira H Ayadi The autosomal recessive isolated deafness, DFNB2, and the Usher 1B syndrome are allelic defects of the myosin-VIIA gene Nat Genet 16 1997 191 193
26. D Weil G Levy I Sahly F Levi-Acobas S Blanchard A El-Amraoui F Crozet Human myosin VIIA responsible for the Usher 1B syndrome: a predicted membrane-associated motor protein expressed in developing sensory epithelia Proc Natl Acad Sci USA 93 1996 3232 3237
27. MD Weston PM Kelley LD Overbeck M Wagenaar DJ Orten T Hasson Z-Y Chen Myosin VIIA mutation screening in 189 Usher syndrome Type 1 patients Am J Hum Genet 59 1996 1074 1083