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A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice
The cilia and cell cycles are inextricably linked. Centrioles in the basal body of cilia nucleate the ciliary axoneme and sequester pericentriolar matrix (PCM) at the centrosome to organize the mitotic spindle. Cilia themselves respond to growth signals, prompting cilia resorption and cell cycle re-...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251972/ https://www.ncbi.nlm.nih.gov/pubmed/30458140 http://dx.doi.org/10.1016/j.devcel.2018.10.027 |
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author | Ford, Matthew J. Yeyati, Patricia L. Mali, Girish R. Keighren, Margaret A. Waddell, Scott H. Mjoseng, Heidi K. Douglas, Adam T. Hall, Emma A. Sakaue-Sawano, Asako Miyawaki, Atsushi Meehan, Richard R. Boulter, Luke Jackson, Ian J. Mill, Pleasantine Mort, Richard L. |
author_facet | Ford, Matthew J. Yeyati, Patricia L. Mali, Girish R. Keighren, Margaret A. Waddell, Scott H. Mjoseng, Heidi K. Douglas, Adam T. Hall, Emma A. Sakaue-Sawano, Asako Miyawaki, Atsushi Meehan, Richard R. Boulter, Luke Jackson, Ian J. Mill, Pleasantine Mort, Richard L. |
author_sort | Ford, Matthew J. |
collection | PubMed |
description | The cilia and cell cycles are inextricably linked. Centrioles in the basal body of cilia nucleate the ciliary axoneme and sequester pericentriolar matrix (PCM) at the centrosome to organize the mitotic spindle. Cilia themselves respond to growth signals, prompting cilia resorption and cell cycle re-entry. We describe a fluorescent cilia and cell cycle biosensor allowing live imaging of cell cycle progression and cilia assembly and disassembly kinetics in cells and inducible mice. We define assembly and disassembly in relation to cell cycle stage with single-cell resolution and explore the intercellular heterogeneity in cilia kinetics. In all cells and tissues analyzed, we observed cilia that persist through the G1/S transition and into S/G2/M-phase. We conclude that persistence of cilia after the G1/S transition is a general property. This resource will shed light at an individual cell level on the interplay between the cilia and cell cycles in development, regeneration, and disease. |
format | Online Article Text |
id | pubmed-6251972 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62519722018-12-03 A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice Ford, Matthew J. Yeyati, Patricia L. Mali, Girish R. Keighren, Margaret A. Waddell, Scott H. Mjoseng, Heidi K. Douglas, Adam T. Hall, Emma A. Sakaue-Sawano, Asako Miyawaki, Atsushi Meehan, Richard R. Boulter, Luke Jackson, Ian J. Mill, Pleasantine Mort, Richard L. Dev Cell Article The cilia and cell cycles are inextricably linked. Centrioles in the basal body of cilia nucleate the ciliary axoneme and sequester pericentriolar matrix (PCM) at the centrosome to organize the mitotic spindle. Cilia themselves respond to growth signals, prompting cilia resorption and cell cycle re-entry. We describe a fluorescent cilia and cell cycle biosensor allowing live imaging of cell cycle progression and cilia assembly and disassembly kinetics in cells and inducible mice. We define assembly and disassembly in relation to cell cycle stage with single-cell resolution and explore the intercellular heterogeneity in cilia kinetics. In all cells and tissues analyzed, we observed cilia that persist through the G1/S transition and into S/G2/M-phase. We conclude that persistence of cilia after the G1/S transition is a general property. This resource will shed light at an individual cell level on the interplay between the cilia and cell cycles in development, regeneration, and disease. Cell Press 2018-11-19 /pmc/articles/PMC6251972/ /pubmed/30458140 http://dx.doi.org/10.1016/j.devcel.2018.10.027 Text en © 2018 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Ford, Matthew J. Yeyati, Patricia L. Mali, Girish R. Keighren, Margaret A. Waddell, Scott H. Mjoseng, Heidi K. Douglas, Adam T. Hall, Emma A. Sakaue-Sawano, Asako Miyawaki, Atsushi Meehan, Richard R. Boulter, Luke Jackson, Ian J. Mill, Pleasantine Mort, Richard L. A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice |
title | A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice |
title_full | A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice |
title_fullStr | A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice |
title_full_unstemmed | A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice |
title_short | A Cell/Cilia Cycle Biosensor for Single-Cell Kinetics Reveals Persistence of Cilia after G1/S Transition Is a General Property in Cells and Mice |
title_sort | cell/cilia cycle biosensor for single-cell kinetics reveals persistence of cilia after g1/s transition is a general property in cells and mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6251972/ https://www.ncbi.nlm.nih.gov/pubmed/30458140 http://dx.doi.org/10.1016/j.devcel.2018.10.027 |
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