Myosin IIIa boosts elongation of stereocilia by transporting espin 1 to the plus ends of actin filaments-Reference-Cited by-同舟云学术

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Myosin IIIa boosts elongation of stereocilia by transporting espin 1 to the plus ends of actin filaments

Published:2009-03-15 Issue:4 Volume:11 Page:443-450
ISSN:1465-7392
Container-title:Nature Cell Biology
language:en
Short-container-title:Nat Cell Biol

Author:

Salles Felipe T.,Merritt Raymond C.,Manor Uri,Dougherty Gerard W.,Sousa Aurea D.,Moore Judy E.,Yengo Christopher M.,Dosé Andréa C.,Kachar Bechara

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

Link

http://www.nature.com/articles/ncb1851.pdf

Reference32 articles.

1. Walsh, T. et al. From flies' eyes to our ears: mutations in a human class III myosin cause progressive non-syndromic hearing loss DFNB30. Proc. Natl Acad. Sci. USA 99, 7518–7523 (2002).

2. Komaba, S., Inoue, A., Maruta, S., Hosoya, H. & Ikebe, M. Determination of human myosin III as a motor protein having a protein kinase activity. J. Biol. Chem. 278, 21352–21360 (2003).

3. Zheng, L. et al. The deaf jerker mouse has a mutation in the gene encoding the espin actin-bundling proteins of hair cell stereocilia and lacks espins. Cell 102, 377–385 (2000).

4. Donaudy, F. et al. Espin gene (ESPN) mutations associated with autosomal dominant hearing loss cause defects in microvillar elongation or organisation. J. Med. Genet. 43, 157–161 (2006).

5. Naz, S. et al. Mutations of ESPN cause autosomal recessive deafness and vestibular dysfunction. J. Med. Genet. 41, 591–595 (2004).

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