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Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis
Distal appendages (DAs) of the mother centriole are essential for the initial steps of ciliogenesis in G1/G0 phase of the cell cycle. DAs are released from centrosomes in mitosis by an undefined mechanism. Here, we show that specific DAs lose their centrosomal localization at the G2/M transition in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055001/ https://www.ncbi.nlm.nih.gov/pubmed/32211891 http://dx.doi.org/10.1083/jcb.201907136 |
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author | Viol, Linda Hata, Shoji Pastor-Peidro, Ana Neuner, Annett Murke, Florian Wuchter, Patrick Ho, Anthony D. Giebel, Bernd Pereira, Gislene |
author_facet | Viol, Linda Hata, Shoji Pastor-Peidro, Ana Neuner, Annett Murke, Florian Wuchter, Patrick Ho, Anthony D. Giebel, Bernd Pereira, Gislene |
author_sort | Viol, Linda |
collection | PubMed |
description | Distal appendages (DAs) of the mother centriole are essential for the initial steps of ciliogenesis in G1/G0 phase of the cell cycle. DAs are released from centrosomes in mitosis by an undefined mechanism. Here, we show that specific DAs lose their centrosomal localization at the G2/M transition in a manner that relies upon Nek2 kinase activity to ensure low DA levels at mitotic centrosomes. Overexpression of active Nek2A, but not kinase-dead Nek2A, prematurely displaced DAs from the interphase centrosomes of immortalized retina pigment epithelial (RPE1) cells. This dramatic impact was also observed in mammary epithelial cells with constitutively high levels of Nek2. Conversely, Nek2 knockout led to incomplete dissociation of DAs and cilia in mitosis. As a consequence, we observed the presence of a cilia remnant that promoted the asymmetric inheritance of ciliary signaling components and supported cilium reassembly after cell division. Together, our data establish Nek2 as an important kinase that regulates DAs before mitosis. |
format | Online Article Text |
id | pubmed-7055001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70550012020-09-02 Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis Viol, Linda Hata, Shoji Pastor-Peidro, Ana Neuner, Annett Murke, Florian Wuchter, Patrick Ho, Anthony D. Giebel, Bernd Pereira, Gislene J Cell Biol Article Distal appendages (DAs) of the mother centriole are essential for the initial steps of ciliogenesis in G1/G0 phase of the cell cycle. DAs are released from centrosomes in mitosis by an undefined mechanism. Here, we show that specific DAs lose their centrosomal localization at the G2/M transition in a manner that relies upon Nek2 kinase activity to ensure low DA levels at mitotic centrosomes. Overexpression of active Nek2A, but not kinase-dead Nek2A, prematurely displaced DAs from the interphase centrosomes of immortalized retina pigment epithelial (RPE1) cells. This dramatic impact was also observed in mammary epithelial cells with constitutively high levels of Nek2. Conversely, Nek2 knockout led to incomplete dissociation of DAs and cilia in mitosis. As a consequence, we observed the presence of a cilia remnant that promoted the asymmetric inheritance of ciliary signaling components and supported cilium reassembly after cell division. Together, our data establish Nek2 as an important kinase that regulates DAs before mitosis. Rockefeller University Press 2020-02-14 /pmc/articles/PMC7055001/ /pubmed/32211891 http://dx.doi.org/10.1083/jcb.201907136 Text en © 2020 Viol 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 Viol, Linda Hata, Shoji Pastor-Peidro, Ana Neuner, Annett Murke, Florian Wuchter, Patrick Ho, Anthony D. Giebel, Bernd Pereira, Gislene Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis |
title | Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis |
title_full | Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis |
title_fullStr | Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis |
title_full_unstemmed | Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis |
title_short | Nek2 kinase displaces distal appendages from the mother centriole prior to mitosis |
title_sort | nek2 kinase displaces distal appendages from the mother centriole prior to mitosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7055001/ https://www.ncbi.nlm.nih.gov/pubmed/32211891 http://dx.doi.org/10.1083/jcb.201907136 |
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