Cargando…
Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA
Cytokinesis is required to physically separate the daughter cells at the end of mitosis. This crucial process requires the assembly and ingression of an actomyosin ring, which must occur with high fidelity to avoid aneuploidy and cell fate changes. Most of our knowledge of mammalian cytokinesis was...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9683116/ https://www.ncbi.nlm.nih.gov/pubmed/36416720 http://dx.doi.org/10.1098/rsob.220247 |
_version_ | 1784835002642464768 |
---|---|
author | Husser, Mathieu C. Ozugergin, Imge Resta, Tiziana Martin, Vincent J. J. Piekny, Alisa J. |
author_facet | Husser, Mathieu C. Ozugergin, Imge Resta, Tiziana Martin, Vincent J. J. Piekny, Alisa J. |
author_sort | Husser, Mathieu C. |
collection | PubMed |
description | Cytokinesis is required to physically separate the daughter cells at the end of mitosis. This crucial process requires the assembly and ingression of an actomyosin ring, which must occur with high fidelity to avoid aneuploidy and cell fate changes. Most of our knowledge of mammalian cytokinesis was generated using over-expressed transgenes in HeLa cells. Over-expression can introduce artefacts, while HeLa are cancerous human cells that have lost their epithelial identity, and the mechanisms controlling cytokinesis in these cells could be vastly different from other cell types. Here, we tagged endogenous anillin, Ect2 and RhoA with mNeonGreen and characterized their localization during cytokinesis for the first time in live human cells. Comparing anillin localization in multiple cell types revealed cytokinetic diversity with differences in the duration and symmetry of ring closure, and the timing of cortical recruitment. Our findings show that the breadth of anillin correlates with the rate of ring closure, and support models where cell size or ploidy affects the cortical organization, and intrinsic mechanisms control the symmetry of ring closure. This work highlights the need to study cytokinesis in more diverse cell types, which will be facilitated by the reagents generated for this study. |
format | Online Article Text |
id | pubmed-9683116 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-96831162022-11-23 Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA Husser, Mathieu C. Ozugergin, Imge Resta, Tiziana Martin, Vincent J. J. Piekny, Alisa J. Open Biol Methods and Techniques Cytokinesis is required to physically separate the daughter cells at the end of mitosis. This crucial process requires the assembly and ingression of an actomyosin ring, which must occur with high fidelity to avoid aneuploidy and cell fate changes. Most of our knowledge of mammalian cytokinesis was generated using over-expressed transgenes in HeLa cells. Over-expression can introduce artefacts, while HeLa are cancerous human cells that have lost their epithelial identity, and the mechanisms controlling cytokinesis in these cells could be vastly different from other cell types. Here, we tagged endogenous anillin, Ect2 and RhoA with mNeonGreen and characterized their localization during cytokinesis for the first time in live human cells. Comparing anillin localization in multiple cell types revealed cytokinetic diversity with differences in the duration and symmetry of ring closure, and the timing of cortical recruitment. Our findings show that the breadth of anillin correlates with the rate of ring closure, and support models where cell size or ploidy affects the cortical organization, and intrinsic mechanisms control the symmetry of ring closure. This work highlights the need to study cytokinesis in more diverse cell types, which will be facilitated by the reagents generated for this study. The Royal Society 2022-11-23 /pmc/articles/PMC9683116/ /pubmed/36416720 http://dx.doi.org/10.1098/rsob.220247 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Methods and Techniques Husser, Mathieu C. Ozugergin, Imge Resta, Tiziana Martin, Vincent J. J. Piekny, Alisa J. Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA |
title | Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA |
title_full | Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA |
title_fullStr | Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA |
title_full_unstemmed | Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA |
title_short | Cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, Ect2 and RhoA |
title_sort | cytokinetic diversity in mammalian cells is revealed by the characterization of endogenous anillin, ect2 and rhoa |
topic | Methods and Techniques |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9683116/ https://www.ncbi.nlm.nih.gov/pubmed/36416720 http://dx.doi.org/10.1098/rsob.220247 |
work_keys_str_mv | AT hussermathieuc cytokineticdiversityinmammaliancellsisrevealedbythecharacterizationofendogenousanillinect2andrhoa AT ozugerginimge cytokineticdiversityinmammaliancellsisrevealedbythecharacterizationofendogenousanillinect2andrhoa AT restatiziana cytokineticdiversityinmammaliancellsisrevealedbythecharacterizationofendogenousanillinect2andrhoa AT martinvincentjj cytokineticdiversityinmammaliancellsisrevealedbythecharacterizationofendogenousanillinect2andrhoa AT pieknyalisaj cytokineticdiversityinmammaliancellsisrevealedbythecharacterizationofendogenousanillinect2andrhoa |