Skip Navigation

This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrow Search for citing articles in:
ISI Web of Science (44)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Kikkawa, Y.
Right arrow Articles by Yonekawa, H.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kikkawa, Y.
Right arrow Articles by Yonekawa, H.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, 2003, Vol. 12, No. 5 453-461
© 2003 Oxford University Press

Mutations in a new scaffold protein Sans cause deafness in Jackson shaker mice

Yoshiaki Kikkawa1, Hiroshi Shitara1, Shigeharu Wakana2, Yuki Kohara1, Toyoyuki Takada1, Mieko Okamoto1, Choji Taya1, Kazusaku Kamiya3, Yasuhiro Yoshikawa3, Hisashi Tokano4, Ken Kitamura4, Kunihiko Shimizu5, Yuichi Wakabayashi6, Toshihiko Shiroishi2,5, Ryo Kominami6 and Hiromichi Yonekawa1,*

1Department of Laboratory Animal Science, The Tokyo Metropolitan Institute of Medical Science (Rinshoken), Tokyo 113-8613, Japan, 2Mouse Functional Genomics Research Group, RIKEN Genome Science Center, The Institute of Physical and Chemical Research, Yokohama 244-0804, Japan, 3Department of Biomedical Science, The University of Tokyo, Tokyo 113-8657, Japan, 4Department of Otolaryngology, Tokyo Medical and Dental University, Tokyo 113-8519, Japan, 5Mammalian Genetics Laboratory, National Institute of Genetics, Mishima 411-8540, Japan and 6Department of Gene Regulation Division of Molecular Biology, Niigata Graduate School of Medicine and Dental Science, Niigata 951-8510, Japan

Received October 1, 2002; Accepted December 13, 2002

The Jackson shaker ( js) mouse carries a recessive mutation causing phenotypes such as deafness, abnormal behavior (circling and/or head-tossing) and degeneration of inner ear neuroepithelia. Two alleles have been identified so far, the original js and jsseal. A contig of three BAC clones was isolated by positional cloning. Two of the clones rescue the js phenotype by BAC transgenesis. Analysis of transcripts in an overlapping region of the two clones revealed a gene encoding a new scaffold-like protein, Sans, that showed mutations in the two js mutants. One was a guanine nucleotide insertion in the original js allele and the other a 7-base insertion in the jsseal allele. Both insertions are predicted to inactivate the Sans protein by frameshift mutations resulting in a truncated protein lacking the C-terminal SAM domain. Cochlear hair cells in the js murtants show disorganized stereocilia bundles, and Sans were highly expressed in inner and outer hair cells of cochlea. The existence of major motifs, ankyrin repeats and a SAM domain suggests that Sans may have an important role in the development and maintenance of the stereocilia bundles through protein–protein interaction.

* To whom correspondence should be addressed. Tel: +81 338232105 (ext. 5103); Fax: +81 338247445; Email: yonekawa{at}rinshoken.or.jp


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Proc. Natl. Acad. Sci. USAHome page
M. Schwander, W. Xiong, J. Tokita, A. Lelli, H. M. Elledge, P. Kazmierczak, A. Sczaniecka, A. Kolatkar, T. Wiltshire, P. Kuhn, et al.
From the Cover: A mouse model for nonsyndromic deafness (DFNB12) links hearing loss to defects in tip links of mechanosensory hair cells
PNAS, March 31, 2009; 106(13): 5252 - 5257.
[Abstract] [Full Text] [PDF]


Home page
DevelopmentHome page
G. Lefevre, V. Michel, D. Weil, L. Lepelletier, E. Bizard, U. Wolfrum, J.-P. Hardelin, and C. Petit
A core cochlear phenotype in USH1 mouse mutants implicates fibrous links of the hair bundle in its cohesion, orientation and differential growth
Development, April 15, 2008; 135(8): 1427 - 1437.
[Abstract] [Full Text] [PDF]


Home page
Proc. Natl. Acad. Sci. USAHome page
X. Liu, O. V. Bulgakov, K. N. Darrow, B. Pawlyk, M. Adamian, M. C. Liberman, and T. Li
Usherin is required for maintenance of retinal photoreceptors and normal development of cochlear hair cells
PNAS, March 13, 2007; 104(11): 4413 - 4418.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
L. H. Gagnon, C. M. Longo-Guess, M. Berryman, J.-B. Shin, K. W. Saylor, H. Yu, P. G. Gillespie, and K. R. Johnson
The Chloride Intracellular Channel Protein CLIC5 Is Expressed at High Levels in Hair Cell Stereocilia and Is Essential for Normal Inner Ear Function
J. Neurosci., October 4, 2006; 26(40): 10188 - 10198.
[Abstract] [Full Text] [PDF]


Home page
IOVSHome page
R. J. L. Haywood-Watson II, Z. M. Ahmed, S. Kjellstrom, R. A. Bush, Y. Takada, L. L. Hampton, J. F. Battey, P. A. Sieving, and T. B. Friedman
Ames waltzer deaf mice have reduced electroretinogram amplitudes and complex alternative splicing of pcdh15 transcripts.
Invest. Ophthalmol. Vis. Sci., July 1, 2006; 47(7): 3074 - 3084.
[Abstract] [Full Text] [PDF]


Home page
J. Am. Soc. Nephrol.Home page
J. H. Brown, M.-T. Bihoreau, S. Hoffmann, B. Kranzlin, I. Tychinskaya, N. Obermuller, D. Podlich, S. N. Boehn, P. J. Kaisaki, N. Megel, et al.
Missense Mutation in Sterile {alpha} Motif of Novel Protein SamCystin is Associated with Polycystic Kidney Disease in (cy/+) Rat
J. Am. Soc. Nephrol., December 1, 2005; 16(12): 3517 - 3526.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
A. El-Amraoui and C. Petit
Usher I syndrome: unravelling the mechanisms that underlie the cohesion of the growing hair bundle in inner ear sensory cells
J. Cell Sci., October 15, 2005; 118(20): 4593 - 4603.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
A. Adato, V. Michel, Y. Kikkawa, J. Reiners, K. N. Alagramam, D. Weil, H. Yonekawa, U. Wolfrum, A. El-Amraoui, and C. Petit
Interactions in the network of Usher syndrome type 1 proteins
Hum. Mol. Genet., February 1, 2005; 14(3): 347 - 356.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
Q. Y. Zheng, D. Yan, X. M. Ouyang, L. L. Du, H. Yu, B. Chang, K. R. Johnson, and X. Z. Liu
Digenic inheritance of deafness caused by mutations in genes encoding cadherin 23 and protocadherin 15 in mice and humans
Hum. Mol. Genet., January 1, 2005; 14(1): 103 - 111.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
M. De Rycker and C. M. Price
Tankyrase Polymerization Is Controlled by Its Sterile Alpha Motif and Poly(ADP-Ribose) Polymerase Domains
Mol. Cell. Biol., November 15, 2004; 24(22): 9802 - 9812.
[Abstract] [Full Text] [PDF]


Home page
GENES CELLSHome page
A. M Johnston, G. Naselli, H. Niwa, T. Brodnicki, L. C Harrison, and L. J. Gonez
Harp (harmonin-interacting, ankyrin repeat-containing protein), a novel protein that interacts with harmonin in epithelial tissues
Genes Cells, October 1, 2004; 9(10): 967 - 982.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
R. D. Hawkins and M. Lovett
The developmental genetics of auditory hair cells
Hum. Mol. Genet., October 1, 2004; 13(suppl_2): R289 - R296.
[Abstract] [Full Text] [PDF]


Home page
JCBHome page
S.-i. Kitajiri, K. Fukumoto, M. Hata, H. Sasaki, T. Katsuno, T. Nakagawa, J. Ito, S. Tsukita, and S. Tsukita
Radixin deficiency causes deafness associated with progressive degeneration of cochlear stereocilia
J. Cell Biol., August 16, 2004; 166(4): 559 - 570.
[Abstract] [Full Text] [PDF]


Home page
Biol. Reprod.Home page
W. Yan, L. Ma, C. A. Zilinski, and M. M. Matzuk
Identification and Characterization of Evolutionarily Conserved Pufferfish, Zebrafish, and Frog Orthologs of GASZ
Biol Reprod, June 1, 2004; 70(6): 1619 - 1625.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
Z. M. Ahmed, S. Riazuddin, J. Ahmad, S. L. Bernstein, Y. Guo, M. F. Sabar, P. Sieving, S. Riazuddin, A. J. Griffith, T. B. Friedman, et al.
PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23
Hum. Mol. Genet., December 15, 2003; 12(24): 3215 - 3223.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
K. R. Johnson, L. H. Gagnon, L. S. Webb, L. L. Peters, N. L. Hawes, B. Chang, and Q. Y. Zheng
Mouse models of USH1C and DFNB18: phenotypic and molecular analyses of two new spontaneous mutations of the Ush1c gene
Hum. Mol. Genet., December 1, 2003; 12(23): 3075 - 3086.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
D. Weil, A. El-Amraoui, S. Masmoudi, M. Mustapha, Y. Kikkawa, S. Laine, S. Delmaghani, A. Adato, S. Nadifi, Z. B. Zina, et al.
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin
Hum. Mol. Genet., March 1, 2003; 12(5): 463 - 471.
[Abstract] [Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.