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Regulation of stereocilia length by myosin XVa and whirlin depends on the actin-regulatory protein Eps8
Authors:Manor Uri  Disanza Andrea  Grati M'Hamed  Andrade Leonardo  Lin Harrison  Di Fiore Pier Paolo  Scita Giorgio  Kachar Bechara
Institution:1 Laboratory of Cell Structure and Dynamics, National Institute on Deafness and Other Communication Disorders, National Institutes of Health, Bethesda, MD 20892, USA
2 Department of Biology, Johns Hopkins University, Baltimore, MD 21218, USA
3 IFOM, The FIRC Institute of Molecular Oncology Foundation, Via Adamello 16, 20139 Milan, Italy
4 Dipartimento di Medicina, Chirurgia ed Odontoiatria, Universita degli Studi di Milano, 20142 Milan, Italy
Abstract:Myosin XVa (MyoXVa) and its cargo whirlin are implicated in deafness and vestibular dysfunction and have been shown to localize at stereocilia tips and to be essential for the elongation of these actin protrusions 1-4]. Given that whirlin has no known actin-regulatory activity, it remains unclear how these proteins work together to influence stereocilia length. Here we show that the actin-regulatory protein Eps8 5] interacts with MyoXVa and that mice lacking Eps8 show short stereocilia compared to MyoXVa- and whirlin-deficient mice. We show that Eps8 fails to accumulate at the tips of stereocilia in the absence of MyoXVa, that overexpression of MyoXVa results in both elongation of stereocilia and increased accumulation of Eps8 at stereocilia tips, and that the exogenous expression of MyoXVa in MyoXVa-deficient hair cells rescues Eps8 tip localization. We find that Eps8 also interacts with whirlin and that the expression of both Eps8 and MyoXVa at stereocilia tips is reduced in whirlin-deficient mice. We conclude that MyoXVa, whirlin, and Eps8 are integral components of the stereocilia tip complex, where Eps8 is a central actin-regulatory element for elongation of the stereocilia actin core.
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