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Myosin 7 and its adaptors link cadherins to actin

Cadherin linkages between adjacent stereocilia and microvilli are essential for mechanotransduction and maintaining their organization. They are anchored to actin through interaction of their cytoplasmic domains with related tripartite complexes consisting of a class VII myosin and adaptor proteins:...

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Autores principales: Yu, I-Mei, Planelles-Herrero, Vicente J., Sourigues, Yannick, Moussaoui, Dihia, Sirkia, Helena, Kikuti, Carlos, Stroebel, David, Titus, Margaret A., Houdusse, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493754/
https://www.ncbi.nlm.nih.gov/pubmed/28660889
http://dx.doi.org/10.1038/ncomms15864
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author Yu, I-Mei
Planelles-Herrero, Vicente J.
Sourigues, Yannick
Moussaoui, Dihia
Sirkia, Helena
Kikuti, Carlos
Stroebel, David
Titus, Margaret A.
Houdusse, Anne
author_facet Yu, I-Mei
Planelles-Herrero, Vicente J.
Sourigues, Yannick
Moussaoui, Dihia
Sirkia, Helena
Kikuti, Carlos
Stroebel, David
Titus, Margaret A.
Houdusse, Anne
author_sort Yu, I-Mei
collection PubMed
description Cadherin linkages between adjacent stereocilia and microvilli are essential for mechanotransduction and maintaining their organization. They are anchored to actin through interaction of their cytoplasmic domains with related tripartite complexes consisting of a class VII myosin and adaptor proteins: Myo7a/SANS/Harmonin in stereocilia and Myo7b/ANKS4B/Harmonin in microvilli. Here, we determine high-resolution structures of Myo7a and Myo7b C-terminal MyTH4-FERM domain (MF2) and unveil how they recognize harmonin using a novel binding mode. Systematic definition of interactions between domains of the tripartite complex elucidates how the complex assembles and prevents possible self-association of harmonin-a. Several Myo7a deafness mutants that map to the surface of MF2 disrupt harmonin binding, revealing the molecular basis for how they impact the formation of the tripartite complex and disrupt mechanotransduction. Our results also suggest how switching between different harmonin isoforms can regulate the formation of networks with Myo7a motors and coordinate force sensing in stereocilia.
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spelling pubmed-54937542017-07-11 Myosin 7 and its adaptors link cadherins to actin Yu, I-Mei Planelles-Herrero, Vicente J. Sourigues, Yannick Moussaoui, Dihia Sirkia, Helena Kikuti, Carlos Stroebel, David Titus, Margaret A. Houdusse, Anne Nat Commun Article Cadherin linkages between adjacent stereocilia and microvilli are essential for mechanotransduction and maintaining their organization. They are anchored to actin through interaction of their cytoplasmic domains with related tripartite complexes consisting of a class VII myosin and adaptor proteins: Myo7a/SANS/Harmonin in stereocilia and Myo7b/ANKS4B/Harmonin in microvilli. Here, we determine high-resolution structures of Myo7a and Myo7b C-terminal MyTH4-FERM domain (MF2) and unveil how they recognize harmonin using a novel binding mode. Systematic definition of interactions between domains of the tripartite complex elucidates how the complex assembles and prevents possible self-association of harmonin-a. Several Myo7a deafness mutants that map to the surface of MF2 disrupt harmonin binding, revealing the molecular basis for how they impact the formation of the tripartite complex and disrupt mechanotransduction. Our results also suggest how switching between different harmonin isoforms can regulate the formation of networks with Myo7a motors and coordinate force sensing in stereocilia. Nature Publishing Group 2017-06-29 /pmc/articles/PMC5493754/ /pubmed/28660889 http://dx.doi.org/10.1038/ncomms15864 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yu, I-Mei
Planelles-Herrero, Vicente J.
Sourigues, Yannick
Moussaoui, Dihia
Sirkia, Helena
Kikuti, Carlos
Stroebel, David
Titus, Margaret A.
Houdusse, Anne
Myosin 7 and its adaptors link cadherins to actin
title Myosin 7 and its adaptors link cadherins to actin
title_full Myosin 7 and its adaptors link cadherins to actin
title_fullStr Myosin 7 and its adaptors link cadherins to actin
title_full_unstemmed Myosin 7 and its adaptors link cadherins to actin
title_short Myosin 7 and its adaptors link cadherins to actin
title_sort myosin 7 and its adaptors link cadherins to actin
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5493754/
https://www.ncbi.nlm.nih.gov/pubmed/28660889
http://dx.doi.org/10.1038/ncomms15864
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