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

被引:350
作者
Boëda, B
El-Amraoui, A
Bahloul, A
Goodyear, R
Daviet, L
Blanchard, S
Perfettini, I
Fath, KR
Shorte, S
Reiners, J
Houdusse, A
Legrain, P
Wolfrum, U
Richardson, G
Petit, C
机构
[1] Inst Pasteur, Unite Genet Deficits Sensoriels, CNRS, URA 1968, F-75724 Paris 15, France
[2] Inst Pasteur, Ctr Imagerie Dynam, F-75724 Paris 15, France
[3] Inst Curie, IC, CNRS, UMR 144, F-75248 Paris 05, France
[4] Hybrigenics, F-75014 Paris, France
[5] Univ Sussex, Sch Biol Sci, Brighton BN1 9QG, E Sussex, England
[6] Johannes Gutenberg Univ Mainz, Inst Zool, D-55099 Mainz, Germany
关键词
cadherin; 23; hair bundle; harmonin; myosin VIIa; Usher syndrome;
D O I
10.1093/emboj/cdf689
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
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.
引用
收藏
页码:6689 / 6699
页数:11
相关论文
共 45 条
[1]
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F [J].
Ahmed, ZM ;
Riazuddin, S ;
Bernstein, SL ;
Ahmed, Z ;
Khan, S ;
Griffith, AJ ;
Morell, RJ ;
Friedman, TB ;
Riazuddin, S ;
Wilcox, ER .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (01) :25-34
[2]
Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F [J].
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 .
HUMAN MOLECULAR GENETICS, 2001, 10 (16) :1709-1718
[3]
The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene [J].
Alagramam, KN ;
Murcia, CL ;
Kwon, HY ;
Pawlowski, KS ;
Wright, CG ;
Woychik, RP .
NATURE GENETICS, 2001, 27 (01) :99-102
[4]
Angst BD, 2001, J CELL SCI, V114, P625
[5]
A millennial myosin census [J].
Berg, JS ;
Powell, BC ;
Cheney, RE .
MOLECULAR BIOLOGY OF THE CELL, 2001, 12 (04) :780-794
[6]
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene [J].
Bitner-Glindzicz, M ;
Lindley, KJ ;
Rutland, P ;
Blaydon, D ;
Smith, VV ;
Milla, PJ ;
Hussain, K ;
Furth-Lavi, J ;
Cosgrove, KE ;
Shepherd, RM ;
Barnes, PD ;
O'Brien, RE ;
Farndon, PA ;
Sowden, J ;
Liu, XZ ;
Scanlan, MJ ;
Malcolm, S ;
Dunne, MJ ;
Aynsley-Green, A ;
Glaser, B .
NATURE GENETICS, 2000, 26 (01) :56-60
[7]
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D [J].
Bolz, H ;
von Brederlow, B ;
Ramírez, A ;
Bryda, EC ;
Kutsche, K ;
Nothwang, HG ;
Seeliger, M ;
Cabrera, MDS ;
Vila, MC ;
Molina, OP ;
Gal, A ;
Kubisch, C .
NATURE GENETICS, 2001, 27 (01) :108-112
[8]
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23 [J].
Bork, JM ;
Peters, LM ;
Riazuddin, S ;
Bernstein, SL ;
Ahmed, ZM ;
Ness, SL ;
Polomeno, R ;
Ramesh, A ;
Schloss, M ;
Srisailpathy, CRS ;
Wayne, S ;
Bellman, S ;
Desmukh, D ;
Ahmed, Z ;
Khan, SN ;
Kaloustian, VMD ;
Li, XC ;
Lalwani, A ;
Riazuddin, S ;
Bitner-Glindzicz, M ;
Nance, WE ;
Liu, XZ ;
Wistow, G ;
Smith, RJH ;
Griffith, AJ ;
Wilcox, ER ;
Friedman, TB ;
Morell, RJ .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 68 (01) :26-37
[9]
Cox B, 2000, DEV DYNAM, V217, P233, DOI 10.1002/(SICI)1097-0177(200003)217:3<233::AID-DVDY1>3.0.CO
[10]
2-O