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Cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus

In the fungus Ustilago maydis, sexual pheromones elicit mating resulting in an infective filament able to infect corn plants. Along this process a G2 cell cycle arrest is mandatory. Such as cell cycle arrest is initiated upon the pheromone recognition in each mating partner, and sustained once cell...

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Autores principales: Bardetti, Paola, Castanheira, Sónia Marisa, Valerius, Oliver, Braus, Gerhard H, Pérez-Martín, José
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6887120/
https://www.ncbi.nlm.nih.gov/pubmed/31621584
http://dx.doi.org/10.7554/eLife.48943
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author Bardetti, Paola
Castanheira, Sónia Marisa
Valerius, Oliver
Braus, Gerhard H
Pérez-Martín, José
author_facet Bardetti, Paola
Castanheira, Sónia Marisa
Valerius, Oliver
Braus, Gerhard H
Pérez-Martín, José
author_sort Bardetti, Paola
collection PubMed
description In the fungus Ustilago maydis, sexual pheromones elicit mating resulting in an infective filament able to infect corn plants. Along this process a G2 cell cycle arrest is mandatory. Such as cell cycle arrest is initiated upon the pheromone recognition in each mating partner, and sustained once cell fusion occurred until the fungus enter the plant tissue. We describe that the initial cell cycle arrest resulted from inhibition of the nuclear transport of the mitotic inducer Cdc25 by targeting its importin, Kap123. Near cell fusion to take place, the increase on pheromone signaling promotes Cdc25 degradation, which seems to be important to ensure the maintenance of the G2 cell cycle arrest to lead the formation of the infective filament. This way, premating cell cycle arrest is linked to the subsequent steps required for establishment of the infection. Disabling this connection resulted in the inability of fungal cells to infect plants.
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spelling pubmed-68871202019-12-04 Cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus Bardetti, Paola Castanheira, Sónia Marisa Valerius, Oliver Braus, Gerhard H Pérez-Martín, José eLife Developmental Biology In the fungus Ustilago maydis, sexual pheromones elicit mating resulting in an infective filament able to infect corn plants. Along this process a G2 cell cycle arrest is mandatory. Such as cell cycle arrest is initiated upon the pheromone recognition in each mating partner, and sustained once cell fusion occurred until the fungus enter the plant tissue. We describe that the initial cell cycle arrest resulted from inhibition of the nuclear transport of the mitotic inducer Cdc25 by targeting its importin, Kap123. Near cell fusion to take place, the increase on pheromone signaling promotes Cdc25 degradation, which seems to be important to ensure the maintenance of the G2 cell cycle arrest to lead the formation of the infective filament. This way, premating cell cycle arrest is linked to the subsequent steps required for establishment of the infection. Disabling this connection resulted in the inability of fungal cells to infect plants. eLife Sciences Publications, Ltd 2019-10-17 /pmc/articles/PMC6887120/ /pubmed/31621584 http://dx.doi.org/10.7554/eLife.48943 Text en © 2019, Bardetti et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Bardetti, Paola
Castanheira, Sónia Marisa
Valerius, Oliver
Braus, Gerhard H
Pérez-Martín, José
Cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus
title Cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus
title_full Cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus
title_fullStr Cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus
title_full_unstemmed Cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus
title_short Cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus
title_sort cytoplasmic retention and degradation of a mitotic inducer enable plant infection by a pathogenic fungus
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6887120/
https://www.ncbi.nlm.nih.gov/pubmed/31621584
http://dx.doi.org/10.7554/eLife.48943
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