Genetic insights into the morphogenesis of inner ear hair cells

被引:166
作者
Frolenkov, GI
Belyantseva, IA
Friedman, TB
Griffith, AJ [1 ]
机构
[1] Natl Inst Deafness & Other Commun Disorders, Sect Gene Struct & Funct, NIH, Rockville, MD 20850 USA
[2] Natl Inst Deafness & Other Commun Disorders, Sect Human Genet, Genet Mol Lab, NIH, Rockville, MD 20850 USA
[3] Natl Inst Deafness & Other Commun Disorders, Hearing Sect, Neurootol Branch, NIH, Rockville, MD 20850 USA
关键词
D O I
10.1038/nrg1377
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The mammalian inner ear is a sensory organ that has specialized hair cells that detect sound, as well as orientation and movement of the head. The 'hair' bundle on the apical surface of these cells is a mechanosensitive organelle that consists of precisely organized actin-filled projections known as stereocilia. Alterations in hair-bundle morphogenesis can result in hearing loss, balance defects or both. Positional cloning of genes that underlie hereditary hearing loss, coupled with the characterization of corresponding mouse models, is revealing how hair cells have adapted the molecular mechanisms of intracellular motility and intercellular adhesion for the morphogenesis of their apical surfaces.
引用
收藏
页码:489 / 498
页数:10
相关论文
共 129 条
  • [1] PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
    Ahmed, ZM
    Riazuddin, S
    Ahmad, J
    Bernstein, SL
    Guo, Y
    Sabar, MF
    Sieving, P
    Riazuddin, S
    Griffith, AJ
    Friedman, TB
    Belyantseva, IA
    Wilcox, ER
    [J]. HUMAN MOLECULAR GENETICS, 2003, 12 (24) : 3215 - 3223
  • [2] Mutations of MYO6 are associated with recessive deafness, DFNB37
    Ahmed, ZM
    Morell, RJ
    Riazuddin, S
    Gropman, A
    Shaukat, S
    Ahmad, MM
    Mohiddin, SA
    Fananapazir, L
    Caruso, RC
    Husnain, T
    Khan, SN
    Riazuddin, S
    Griffith, AJ
    Friedman, TB
    Wilcox, ER
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 72 (05) : 1315 - 1322
  • [3] Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F
    Ahmed, ZM
    Riazuddin, S
    Bernstein, SL
    Ahmed, Z
    Khan, S
    Griffith, AJ
    Morell, RJ
    Friedman, TB
    Riazuddin, S
    Wilcox, ER
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (01) : 25 - 34
  • [4] Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F
    Alagramam, KN
    Yuan, HJ
    Kuehn, MH
    Murcia, CL
    Wayne, S
    Srisailpathy, CRS
    Lowry, RB
    Knaus, R
    Van Laer, L
    Bernier, FP
    Schwartz, S
    Lee, C
    Morton, CC
    Mullins, RF
    Ramesh, A
    Van Camp, G
    Hagemen, GS
    Woychik, RP
    Smith, RJH
    [J]. HUMAN MOLECULAR GENETICS, 2001, 10 (16) : 1709 - 1718
  • [5] The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene
    Alagramam, KN
    Murcia, CL
    Kwon, HY
    Pawlowski, KS
    Wright, CG
    Woychik, RP
    [J]. NATURE GENETICS, 2001, 27 (01) : 99 - 102
  • [6] Neuroepithelial defects of the inner ear in a new allele of the mouse mutation Ames waltzer
    Alagramam, KN
    Zahorsky-Reeves, J
    Wright, CG
    Pawlowski, KS
    Erway, LC
    Stubbs, L
    Woychik, RP
    [J]. HEARING RESEARCH, 2000, 148 (1-2) : 181 - 191
  • [7] The mechanism of myosin VI translocation an its load-induced anchoring
    Altman, D
    Sweeney, HL
    Spudich, JA
    [J]. CELL, 2004, 116 (05) : 737 - 749
  • [8] VESTIBULAR HAIR CELL PATHOLOGY IN THE SHAKER-2 MOUSE
    ANNIKO, M
    SOBIN, A
    WERSALL, J
    [J]. ARCHIVES OF OTO-RHINO-LARYNGOLOGY-ARCHIV FUR OHREN-NASEN-UND KEHLKOPFHEILKUNDE, 1980, 226 (1-2): : 45 - 50
  • [9] TIP-LINK INTEGRITY AND MECHANICAL TRANSDUCTION IN VERTEBRATE HAIR-CELLS
    ASSAD, JA
    SHEPHERD, GMG
    COREY, DP
    [J]. NEURON, 1991, 7 (06) : 985 - 994
  • [10] THE MOUSE SNELLS WALTZER DEAFNESS GENE ENCODES AN UNCONVENTIONAL MYOSIN REQUIRED FOR STRUCTURAL INTEGRITY OF INNER-EAR HAIR-CELLS
    AVRAHAM, KB
    HASSON, T
    STEEL, KP
    KINGSLEY, DM
    RUSSELL, LB
    MOOSEKER, MS
    COPELAND, NG
    JENKINS, NA
    [J]. NATURE GENETICS, 1995, 11 (04) : 369 - 375