2010 Fiscal Year Final Research Report
Establishment and characterization of mouse models for hearing loss based on Molecular interaction
Project/Area Number |
20300147
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Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
Laboratory animal science
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Research Institution | Tokyo University of Agriculture |
Principal Investigator |
KIKKAWA Yoshiaki Tokyo University of Agriculture, 生物産業学部, 准教授 (20280787)
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Co-Investigator(Kenkyū-buntansha) |
SHITARA Hiroshi (財)東京都医学研究機構, 東京都臨床医学総合研究所, 研究員 (90321885)
NOGUCHI Yoshihiro 東京医科歯科大学, 医学部付属病院, 講師 (50282752)
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Research Collaborator |
STEVE Brown 英国MRC, Mammalian Genetics Unit, 教授
奥村 和弘 東京農業大学, 大学院, 博士後期課程
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Project Period (FY) |
2008 – 2010
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Keywords | 育種遺伝 / 分子間相互作用 / 難聴 / マウス / 有毛細胞 / Stereocilia |
Research Abstract |
To establish new mouse models for deafness and identify molecular mechanism of hearing impairment, we carried out positional cloning approach, expression analysis of the inner ear hair cells and protein-protein interaction studies among the deafness associated-proteins. 1) We identified that responsible gene of two new spontaneous mutants is myosin VI. 2) 4.1B and gelsolin may be members of the myosin XV-whirlin complex that is important for stereocilia maturation. 3) Phenotypic data of double homozygotes between Sans and Whrlin mutants suggest that the function of SANS interacts with WHRLIN and the interaction play regulation of planar cell polarity in stereocilia of the hair cells.
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Research Products
(22 results)
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[Journal Article] Phenotypic and expression analysis of a novel spontaneous Myosin VI null mutant mouse.2010
Author(s)
Mochizuki E., Okumura K., Ishikawa M., Yoshimoto S., Yamaguchi J., Seki Y., Wada K., Yokohama M., Ushiki T., Tokano H., Ishii R., Shitara H., Taya C., Kitamura K., Yonekawa H., Kikkawa Y.
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Journal Title
Exp.Anim. 59
Pages: 57-71
Peer Reviewed
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