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Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation

Stereocilia are actin-based cell protrusions of inner ear hair cells and are indispensable for mechanotransduction. Ankle links connect the ankle region of developing stereocilia, playing an essential role in stereocilia development. WHRN, PDZD7, ADGRV1 and USH2A have been identified to form the so-...

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Autores principales: Wang, Huang, Du, Haibo, Ren, Rui, Du, Tingting, Lin, Lin, Feng, Zhe, Zhao, Dange, Wei, Xiaoxi, Zhai, Xiaoyan, Wang, Hongyang, Dong, Tingting, Sun, Jin-Peng, Wu, Hao, Xu, Zhigang, Lu, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039067/
https://www.ncbi.nlm.nih.gov/pubmed/36964137
http://dx.doi.org/10.1038/s41467-023-37267-5
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author Wang, Huang
Du, Haibo
Ren, Rui
Du, Tingting
Lin, Lin
Feng, Zhe
Zhao, Dange
Wei, Xiaoxi
Zhai, Xiaoyan
Wang, Hongyang
Dong, Tingting
Sun, Jin-Peng
Wu, Hao
Xu, Zhigang
Lu, Qing
author_facet Wang, Huang
Du, Haibo
Ren, Rui
Du, Tingting
Lin, Lin
Feng, Zhe
Zhao, Dange
Wei, Xiaoxi
Zhai, Xiaoyan
Wang, Hongyang
Dong, Tingting
Sun, Jin-Peng
Wu, Hao
Xu, Zhigang
Lu, Qing
author_sort Wang, Huang
collection PubMed
description Stereocilia are actin-based cell protrusions of inner ear hair cells and are indispensable for mechanotransduction. Ankle links connect the ankle region of developing stereocilia, playing an essential role in stereocilia development. WHRN, PDZD7, ADGRV1 and USH2A have been identified to form the so-called ankle link complex (ALC); however, the detailed mechanism underlying the temporal emergence and degeneration of ankle links remains elusive. Here we show that WHRN and PDZD7 orchestrate ADGRV1 and USH2A to assemble the ALC through liquid-liquid phase separation (LLPS). Disruption of the ALC multivalency for LLPS largely abolishes the distribution of WHRN at the ankle region of stereocilia. Interestingly, high concentration of ADGRV1 inhibits LLPS, providing a potential mechanism for ALC disassembly. Moreover, certain deafness mutations of ALC genes weaken the multivalent interactions of ALC and impair LLPS. In conclusion, our study demonstrates that LLPS mediates ALC formation, providing essential clues for understanding the pathogenesis of deafness.
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spelling pubmed-100390672023-03-26 Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation Wang, Huang Du, Haibo Ren, Rui Du, Tingting Lin, Lin Feng, Zhe Zhao, Dange Wei, Xiaoxi Zhai, Xiaoyan Wang, Hongyang Dong, Tingting Sun, Jin-Peng Wu, Hao Xu, Zhigang Lu, Qing Nat Commun Article Stereocilia are actin-based cell protrusions of inner ear hair cells and are indispensable for mechanotransduction. Ankle links connect the ankle region of developing stereocilia, playing an essential role in stereocilia development. WHRN, PDZD7, ADGRV1 and USH2A have been identified to form the so-called ankle link complex (ALC); however, the detailed mechanism underlying the temporal emergence and degeneration of ankle links remains elusive. Here we show that WHRN and PDZD7 orchestrate ADGRV1 and USH2A to assemble the ALC through liquid-liquid phase separation (LLPS). Disruption of the ALC multivalency for LLPS largely abolishes the distribution of WHRN at the ankle region of stereocilia. Interestingly, high concentration of ADGRV1 inhibits LLPS, providing a potential mechanism for ALC disassembly. Moreover, certain deafness mutations of ALC genes weaken the multivalent interactions of ALC and impair LLPS. In conclusion, our study demonstrates that LLPS mediates ALC formation, providing essential clues for understanding the pathogenesis of deafness. Nature Publishing Group UK 2023-03-24 /pmc/articles/PMC10039067/ /pubmed/36964137 http://dx.doi.org/10.1038/s41467-023-37267-5 Text en © The Author(s) 2023 https://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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Huang
Du, Haibo
Ren, Rui
Du, Tingting
Lin, Lin
Feng, Zhe
Zhao, Dange
Wei, Xiaoxi
Zhai, Xiaoyan
Wang, Hongyang
Dong, Tingting
Sun, Jin-Peng
Wu, Hao
Xu, Zhigang
Lu, Qing
Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation
title Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation
title_full Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation
title_fullStr Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation
title_full_unstemmed Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation
title_short Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation
title_sort temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10039067/
https://www.ncbi.nlm.nih.gov/pubmed/36964137
http://dx.doi.org/10.1038/s41467-023-37267-5
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