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Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia

Mechanoreceptor cells develop a specialized cytoskeleton that plays structural and sensory roles at the site of mechanotransduction. However, little is known about how the cytoskeleton is organized and formed. Using electron tomography and live-cell imaging, we resolve the 3D structure and dynamics...

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Autores principales: Sun, Landi, Cui, Lihong, Liu, Zhen, Wang, Qixuan, Xue, Zhaoyu, Wu, Menghua, Sun, Tianhui, Mao, Decai, Ni, Jianquan, Pastor-Pareja, José Carlos, Liang, Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Rockefeller University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717695/
https://www.ncbi.nlm.nih.gov/pubmed/33263729
http://dx.doi.org/10.1083/jcb.202004184
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author Sun, Landi
Cui, Lihong
Liu, Zhen
Wang, Qixuan
Xue, Zhaoyu
Wu, Menghua
Sun, Tianhui
Mao, Decai
Ni, Jianquan
Pastor-Pareja, José Carlos
Liang, Xin
author_facet Sun, Landi
Cui, Lihong
Liu, Zhen
Wang, Qixuan
Xue, Zhaoyu
Wu, Menghua
Sun, Tianhui
Mao, Decai
Ni, Jianquan
Pastor-Pareja, José Carlos
Liang, Xin
author_sort Sun, Landi
collection PubMed
description Mechanoreceptor cells develop a specialized cytoskeleton that plays structural and sensory roles at the site of mechanotransduction. However, little is known about how the cytoskeleton is organized and formed. Using electron tomography and live-cell imaging, we resolve the 3D structure and dynamics of the microtubule-based cytoskeleton in fly campaniform mechanosensory cilia. Investigating the formation of the cytoskeleton, we find that katanin p60-like 1 (kat-60L1), a neuronal type of microtubule-severing enzyme, serves two functions. First, it amplifies the mass of microtubules to form the dense microtubule arrays inside the sensory cilia. Second, it generates short microtubules that are required to build the nanoscopic cytoskeleton at the mechanotransduction site. Additional analyses further reveal the functional roles of Patronin and other potential factors in the local regulatory network. In all, our results characterize the specialized cytoskeleton in fly external mechanosensory cilia at near-molecular resolution and provide mechanistic insights into how it is formed.
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spelling pubmed-77176952021-07-04 Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia Sun, Landi Cui, Lihong Liu, Zhen Wang, Qixuan Xue, Zhaoyu Wu, Menghua Sun, Tianhui Mao, Decai Ni, Jianquan Pastor-Pareja, José Carlos Liang, Xin J Cell Biol Article Mechanoreceptor cells develop a specialized cytoskeleton that plays structural and sensory roles at the site of mechanotransduction. However, little is known about how the cytoskeleton is organized and formed. Using electron tomography and live-cell imaging, we resolve the 3D structure and dynamics of the microtubule-based cytoskeleton in fly campaniform mechanosensory cilia. Investigating the formation of the cytoskeleton, we find that katanin p60-like 1 (kat-60L1), a neuronal type of microtubule-severing enzyme, serves two functions. First, it amplifies the mass of microtubules to form the dense microtubule arrays inside the sensory cilia. Second, it generates short microtubules that are required to build the nanoscopic cytoskeleton at the mechanotransduction site. Additional analyses further reveal the functional roles of Patronin and other potential factors in the local regulatory network. In all, our results characterize the specialized cytoskeleton in fly external mechanosensory cilia at near-molecular resolution and provide mechanistic insights into how it is formed. Rockefeller University Press 2020-12-02 /pmc/articles/PMC7717695/ /pubmed/33263729 http://dx.doi.org/10.1083/jcb.202004184 Text en © 2020 Sun et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Sun, Landi
Cui, Lihong
Liu, Zhen
Wang, Qixuan
Xue, Zhaoyu
Wu, Menghua
Sun, Tianhui
Mao, Decai
Ni, Jianquan
Pastor-Pareja, José Carlos
Liang, Xin
Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia
title Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia
title_full Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia
title_fullStr Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia
title_full_unstemmed Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia
title_short Katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia
title_sort katanin p60-like 1 sculpts the cytoskeleton in mechanosensory cilia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7717695/
https://www.ncbi.nlm.nih.gov/pubmed/33263729
http://dx.doi.org/10.1083/jcb.202004184
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