The tip-link antigen, a protein associated with the transduction complex of sensory hair cells, is protocadherin-15

被引:215
作者
Ahmed, Zubair M.
Goodyear, Richard
Riazuddin, Saima
Lagziel, Ayala
Legan, P. Kevin
Behra, Martine
Burgess, Shawn M.
Lilley, Kathryn S.
Wilcox, Edward R.
Riazuddin, Sheikh
Griffith, Andrew J.
Frolenkov, Gregory I.
Belyantseva, Inna A.
Richardson, Guy P. [1 ]
Friedman, Thomas B.
机构
[1] Univ Sussex, Sch Life Sci, Brighton BN1 9QG, E Sussex, England
[2] Natl Inst Deafness & Other Commun Disorders, Lab Mol Genet, NIH, Rockville, MD 20850 USA
[3] NHGRI, Genome Technol Branch, NIH, Bethesda, MD 20892 USA
[4] Univ Cambridge, Dept Biochem, Cambridge Ctr Proteom, Cambridge CB2 1QW, England
[5] Brigham Young Univ, DNA Sequencing Ctr, Dept Integrat Biol, Provo, UT 84602 USA
[6] Natl Ctr Excellence Mol Biol, Lahore, Pakistan
[7] Univ Kentucky, Dept Physiol, Lexington, KY 40536 USA
基金
英国惠康基金;
关键词
protocadherin-15; tip link; TLA; stereocilia; mechanotransduction; hair cell;
D O I
10.1523/JNEUROSCI.1163-06.2006
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sound and acceleration are detected by hair bundles, mechanosensory structures located at the apical pole of hair cells in the inner ear. The different elements of the hair bundle, the stereocilia and a kinocilium, are interconnected by a variety of link types. One of these links, the tip link, connects the top of a shorter stereocilium with the lateral membrane of an adjacent taller stereocilium and may gate the mechanotransducer channel of the hair cell. Mass spectrometric and Western blot analyses identify the tip-link antigen, a hitherto unidentified antigen specifically associated with the tip and kinocilial links of sensory hair bundles in the inner ear and the ciliary calyx of photoreceptors in the eye, as an avian ortholog of human protocadherin-15, a product of the gene for the deaf/blindness Usher syndrome type 1F/DFNB23 locus. Multiple protocadherin-15 transcripts are shown to be expressed in the mouse inner ear, and these define four major isoform classes, two with entirely novel, previously unidentified cytoplasmic domains. Antibodies to the three cytoplasmic domain-containing isoform classes reveal that each has a different spatiotemporal expression pattern in the developing and mature inner ear. Two isoforms are distributed in a manner compatible for association with the tip-link complex. An isoform located at the tips of stereocilia is sensitive to calcium chelation and proteolysis with subtilisin and reappears at the tips of stereocilia as transduction recovers after the removal of calcium chelators. Protocadherin-15 is therefore associated with the tip-link complex and may be an integral component of this structure and/or required for its formation.
引用
收藏
页码:7022 / 7034
页数:13
相关论文
共 36 条
[1]   Interactions in the network of Usher syndrome type 1 proteins [J].
Adato, A ;
Michel, V ;
Kikkawa, Y ;
Reiners, J ;
Alagramam, KN ;
Weil, D ;
Yonekawa, H ;
Wolfrum, U ;
El-Amraoui, A ;
Petit, C .
HUMAN MOLECULAR GENETICS, 2005, 14 (03) :347-356
[2]   PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23 [J].
Ahmed, ZM ;
Riazuddin, S ;
Ahmad, J ;
Bernstein, SL ;
Guo, Y ;
Sabar, MF ;
Sieving, P ;
Riazuddin, S ;
Griffith, AJ ;
Friedman, TB ;
Belyantseva, IA ;
Wilcox, ER .
HUMAN MOLECULAR GENETICS, 2003, 12 (24) :3215-3223
[3]   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
[4]   Characterization of vestibular dysfunction in the mouse model for Usher syndrome 1F [J].
Alagramam, KN ;
Stahl, JS ;
Jones, SM ;
Pawlowski, KS ;
Wright, CG .
JARO-JOURNAL OF THE ASSOCIATION FOR RESEARCH IN OTOLARYNGOLOGY, 2005, 6 (02) :106-118
[5]   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
[6]   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
[7]   TIP-LINK INTEGRITY AND MECHANICAL TRANSDUCTION IN VERTEBRATE HAIR-CELLS [J].
ASSAD, JA ;
SHEPHERD, GMG ;
COREY, DP .
NEURON, 1991, 7 (06) :985-994
[8]   APPEARANCE AND DISTRIBUTION OF THE 275 KD HAIR-CELL ANTIGEN DURING DEVELOPMENT OF THE AVIAN INNER-EAR [J].
BARTOLAMI, S ;
GOODYEAR, R ;
RICHARDSON, G .
JOURNAL OF COMPARATIVE NEUROLOGY, 1991, 314 (04) :777-788
[9]   Myosin-XVa is required for tip localization of whirlin and differential elongation of hair-cell stereocilia [J].
Belyantseva, IA ;
Boger, ET ;
Naz, S ;
Frolenkov, GI ;
Sellers, JR ;
Ahmed, ZM ;
Griffith, AJ ;
Friedman, TB .
NATURE CELL BIOLOGY, 2005, 7 (02) :148-U60
[10]   Brief report - A mutation of PCDH15 among Ashkenazi Jews with the type 1 Usher syndrome [J].
Ben-Yosef, T ;
Ness, SL ;
Madeo, AC ;
Bar-Lev, A ;
Wolfman, JH ;
Ahmed, ZM ;
Desnick, RJ ;
Willner, JP ;
Avraham, KB ;
Ostrer, H ;
Oddoux, C ;
Griffith, AJ ;
Friedman, TB .
NEW ENGLAND JOURNAL OF MEDICINE, 2003, 348 (17) :1664-1670