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Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo
The last stage of cell division involves two daughter cells remaining interconnected by a cytokinetic bridge that is cleaved during abscission. Conserved between the zebrafish embryo and human cells, we found that the oldest centrosome moves in a Rab11-dependent manner towards the cytokinetic bridge...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933627/ https://www.ncbi.nlm.nih.gov/pubmed/35304423 http://dx.doi.org/10.26508/lsa.202201362 |
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author | Krishnan, Nikhila Swoger, Maxx Rathbun, Lindsay I Fioramonti, Peter J Freshour, Judy Bates, Michael Patteson, Alison E Hehnly, Heidi |
author_facet | Krishnan, Nikhila Swoger, Maxx Rathbun, Lindsay I Fioramonti, Peter J Freshour, Judy Bates, Michael Patteson, Alison E Hehnly, Heidi |
author_sort | Krishnan, Nikhila |
collection | PubMed |
description | The last stage of cell division involves two daughter cells remaining interconnected by a cytokinetic bridge that is cleaved during abscission. Conserved between the zebrafish embryo and human cells, we found that the oldest centrosome moves in a Rab11-dependent manner towards the cytokinetic bridge sometimes followed by the youngest. Rab11-endosomes are organized in a Rab11-GTP dependent manner at the mother centriole during pre-abscission, with Rab11 endosomes at the oldest centrosome being more mobile compared with the youngest. The GTPase activity of Rab11 is necessary for the centrosome protein, Pericentrin, to be enriched at the centrosome. Reduction in Pericentrin expression or optogenetic disruption of Rab11-endosome function inhibited both centrosome movement towards the cytokinetic bridge and abscission, resulting in daughter cells prone to being binucleated and/or having supernumerary centrosomes. These studies suggest that Rab11-endosomes contribute to centrosome function during pre-abscission by regulating Pericentrin organization resulting in appropriate centrosome movement towards the cytokinetic bridge and subsequent abscission. |
format | Online Article Text |
id | pubmed-8933627 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-89336272022-03-25 Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo Krishnan, Nikhila Swoger, Maxx Rathbun, Lindsay I Fioramonti, Peter J Freshour, Judy Bates, Michael Patteson, Alison E Hehnly, Heidi Life Sci Alliance Research Articles The last stage of cell division involves two daughter cells remaining interconnected by a cytokinetic bridge that is cleaved during abscission. Conserved between the zebrafish embryo and human cells, we found that the oldest centrosome moves in a Rab11-dependent manner towards the cytokinetic bridge sometimes followed by the youngest. Rab11-endosomes are organized in a Rab11-GTP dependent manner at the mother centriole during pre-abscission, with Rab11 endosomes at the oldest centrosome being more mobile compared with the youngest. The GTPase activity of Rab11 is necessary for the centrosome protein, Pericentrin, to be enriched at the centrosome. Reduction in Pericentrin expression or optogenetic disruption of Rab11-endosome function inhibited both centrosome movement towards the cytokinetic bridge and abscission, resulting in daughter cells prone to being binucleated and/or having supernumerary centrosomes. These studies suggest that Rab11-endosomes contribute to centrosome function during pre-abscission by regulating Pericentrin organization resulting in appropriate centrosome movement towards the cytokinetic bridge and subsequent abscission. Life Science Alliance LLC 2022-03-18 /pmc/articles/PMC8933627/ /pubmed/35304423 http://dx.doi.org/10.26508/lsa.202201362 Text en © 2022 Krishnan et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Krishnan, Nikhila Swoger, Maxx Rathbun, Lindsay I Fioramonti, Peter J Freshour, Judy Bates, Michael Patteson, Alison E Hehnly, Heidi Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo |
title | Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo |
title_full | Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo |
title_fullStr | Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo |
title_full_unstemmed | Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo |
title_short | Rab11 endosomes and Pericentrin coordinate centrosome movement during pre-abscission in vivo |
title_sort | rab11 endosomes and pericentrin coordinate centrosome movement during pre-abscission in vivo |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8933627/ https://www.ncbi.nlm.nih.gov/pubmed/35304423 http://dx.doi.org/10.26508/lsa.202201362 |
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