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Hydrodynamic Shape Changes Underpin Nuclear Rerouting in Branched Hyphae of an Oomycete Pathogen

Multinucleate fungi and oomycetes are phylogenetically distant but structurally similar. To address whether they share similar nuclear dynamics, we carried out time-lapse imaging of fluorescently labeled Phytophthora palmivora nuclei. Nuclei underwent coordinated bidirectional movements during plant...

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Autores principales: Evangelisti, Edouard, Shenhav, Liron, Yunusov, Temur, Le Naour–Vernet, Marie, Rink, Philipp, Schornack, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775453/
https://www.ncbi.nlm.nih.gov/pubmed/31575765
http://dx.doi.org/10.1128/mBio.01516-19
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author Evangelisti, Edouard
Shenhav, Liron
Yunusov, Temur
Le Naour–Vernet, Marie
Rink, Philipp
Schornack, Sebastian
author_facet Evangelisti, Edouard
Shenhav, Liron
Yunusov, Temur
Le Naour–Vernet, Marie
Rink, Philipp
Schornack, Sebastian
author_sort Evangelisti, Edouard
collection PubMed
description Multinucleate fungi and oomycetes are phylogenetically distant but structurally similar. To address whether they share similar nuclear dynamics, we carried out time-lapse imaging of fluorescently labeled Phytophthora palmivora nuclei. Nuclei underwent coordinated bidirectional movements during plant infection. Within hyphal networks growing in planta or in axenic culture, nuclei either are dragged passively with the cytoplasm or actively become rerouted toward nucleus-depleted hyphal sections and often display a very stretched shape. Benomyl-induced depolymerization of microtubules reduced active movements and the occurrence of stretched nuclei. A centrosome protein localized at the leading end of stretched nuclei, suggesting that, as in fungi, astral microtubule-guided movements contribute to nuclear distribution within oomycete hyphae. The remarkable hydrodynamic shape adaptations of Phytophthora nuclei contrast with those in fungi and likely enable them to migrate over longer distances. Therefore, our work summarizes mechanisms which enable a near-equal nuclear distribution in an oomycete. We provide a basis for computational modeling of hydrodynamic nuclear deformation within branched tubular networks.
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spelling pubmed-67754532019-10-15 Hydrodynamic Shape Changes Underpin Nuclear Rerouting in Branched Hyphae of an Oomycete Pathogen Evangelisti, Edouard Shenhav, Liron Yunusov, Temur Le Naour–Vernet, Marie Rink, Philipp Schornack, Sebastian mBio Research Article Multinucleate fungi and oomycetes are phylogenetically distant but structurally similar. To address whether they share similar nuclear dynamics, we carried out time-lapse imaging of fluorescently labeled Phytophthora palmivora nuclei. Nuclei underwent coordinated bidirectional movements during plant infection. Within hyphal networks growing in planta or in axenic culture, nuclei either are dragged passively with the cytoplasm or actively become rerouted toward nucleus-depleted hyphal sections and often display a very stretched shape. Benomyl-induced depolymerization of microtubules reduced active movements and the occurrence of stretched nuclei. A centrosome protein localized at the leading end of stretched nuclei, suggesting that, as in fungi, astral microtubule-guided movements contribute to nuclear distribution within oomycete hyphae. The remarkable hydrodynamic shape adaptations of Phytophthora nuclei contrast with those in fungi and likely enable them to migrate over longer distances. Therefore, our work summarizes mechanisms which enable a near-equal nuclear distribution in an oomycete. We provide a basis for computational modeling of hydrodynamic nuclear deformation within branched tubular networks. American Society for Microbiology 2019-10-01 /pmc/articles/PMC6775453/ /pubmed/31575765 http://dx.doi.org/10.1128/mBio.01516-19 Text en Copyright © 2019 Evangelisti et al. https://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Evangelisti, Edouard
Shenhav, Liron
Yunusov, Temur
Le Naour–Vernet, Marie
Rink, Philipp
Schornack, Sebastian
Hydrodynamic Shape Changes Underpin Nuclear Rerouting in Branched Hyphae of an Oomycete Pathogen
title Hydrodynamic Shape Changes Underpin Nuclear Rerouting in Branched Hyphae of an Oomycete Pathogen
title_full Hydrodynamic Shape Changes Underpin Nuclear Rerouting in Branched Hyphae of an Oomycete Pathogen
title_fullStr Hydrodynamic Shape Changes Underpin Nuclear Rerouting in Branched Hyphae of an Oomycete Pathogen
title_full_unstemmed Hydrodynamic Shape Changes Underpin Nuclear Rerouting in Branched Hyphae of an Oomycete Pathogen
title_short Hydrodynamic Shape Changes Underpin Nuclear Rerouting in Branched Hyphae of an Oomycete Pathogen
title_sort hydrodynamic shape changes underpin nuclear rerouting in branched hyphae of an oomycete pathogen
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6775453/
https://www.ncbi.nlm.nih.gov/pubmed/31575765
http://dx.doi.org/10.1128/mBio.01516-19
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