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Haspin Modulates the G2/M Transition Delay in Response to Polarization Failures in Budding Yeast
Symmetry breaking by cellular polarization is an exquisite requirement for the cell-cycle of Saccharomyces cerevisiae cells, as it allows bud emergence and growth. This process is based on the formation of polarity clusters at the incipient bud site, first, and the bud tip later in the cell-cycle, t...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876276/ https://www.ncbi.nlm.nih.gov/pubmed/33585466 http://dx.doi.org/10.3389/fcell.2020.625717 |
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author | Galli, Martina Diani, Laura Quadri, Roberto Nespoli, Alessandro Galati, Elena Panigada, Davide Plevani, Paolo Muzi-Falconi, Marco |
author_facet | Galli, Martina Diani, Laura Quadri, Roberto Nespoli, Alessandro Galati, Elena Panigada, Davide Plevani, Paolo Muzi-Falconi, Marco |
author_sort | Galli, Martina |
collection | PubMed |
description | Symmetry breaking by cellular polarization is an exquisite requirement for the cell-cycle of Saccharomyces cerevisiae cells, as it allows bud emergence and growth. This process is based on the formation of polarity clusters at the incipient bud site, first, and the bud tip later in the cell-cycle, that overall promote bud emission and growth. Given the extreme relevance of this process, a surveillance mechanism, known as the morphogenesis checkpoint, has evolved to coordinate the formation of the bud and cell cycle progression, delaying mitosis in the presence of morphogenetic problems. The atypical protein kinase haspin is responsible for histone H3-T3 phosphorylation and, in yeast, for resolution of polarity clusters in mitosis. Here, we report a novel role for haspin in the regulation of the morphogenesis checkpoint in response to polarity insults. Particularly, we show that cells lacking the haspin ortholog Alk1 fail to achieve sustained checkpoint activation and enter mitosis even in the absence of a bud. In alk1Δ cells, we report a reduced phosphorylation of Cdc28-Y19, which stems from a premature activation of the Mih1 phosphatase. Overall, the data presented in this work define yeast haspin as a novel regulator of the morphogenesis checkpoint in Saccharomyces cerevisiae, where it monitors polarity establishment and it couples bud emergence to the G2/M cell cycle transition. |
format | Online Article Text |
id | pubmed-7876276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78762762021-02-12 Haspin Modulates the G2/M Transition Delay in Response to Polarization Failures in Budding Yeast Galli, Martina Diani, Laura Quadri, Roberto Nespoli, Alessandro Galati, Elena Panigada, Davide Plevani, Paolo Muzi-Falconi, Marco Front Cell Dev Biol Cell and Developmental Biology Symmetry breaking by cellular polarization is an exquisite requirement for the cell-cycle of Saccharomyces cerevisiae cells, as it allows bud emergence and growth. This process is based on the formation of polarity clusters at the incipient bud site, first, and the bud tip later in the cell-cycle, that overall promote bud emission and growth. Given the extreme relevance of this process, a surveillance mechanism, known as the morphogenesis checkpoint, has evolved to coordinate the formation of the bud and cell cycle progression, delaying mitosis in the presence of morphogenetic problems. The atypical protein kinase haspin is responsible for histone H3-T3 phosphorylation and, in yeast, for resolution of polarity clusters in mitosis. Here, we report a novel role for haspin in the regulation of the morphogenesis checkpoint in response to polarity insults. Particularly, we show that cells lacking the haspin ortholog Alk1 fail to achieve sustained checkpoint activation and enter mitosis even in the absence of a bud. In alk1Δ cells, we report a reduced phosphorylation of Cdc28-Y19, which stems from a premature activation of the Mih1 phosphatase. Overall, the data presented in this work define yeast haspin as a novel regulator of the morphogenesis checkpoint in Saccharomyces cerevisiae, where it monitors polarity establishment and it couples bud emergence to the G2/M cell cycle transition. Frontiers Media S.A. 2021-01-28 /pmc/articles/PMC7876276/ /pubmed/33585466 http://dx.doi.org/10.3389/fcell.2020.625717 Text en Copyright © 2021 Galli, Diani, Quadri, Nespoli, Galati, Panigada, Plevani and Muzi-Falconi. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cell and Developmental Biology Galli, Martina Diani, Laura Quadri, Roberto Nespoli, Alessandro Galati, Elena Panigada, Davide Plevani, Paolo Muzi-Falconi, Marco Haspin Modulates the G2/M Transition Delay in Response to Polarization Failures in Budding Yeast |
title | Haspin Modulates the G2/M Transition Delay in Response to Polarization Failures in Budding Yeast |
title_full | Haspin Modulates the G2/M Transition Delay in Response to Polarization Failures in Budding Yeast |
title_fullStr | Haspin Modulates the G2/M Transition Delay in Response to Polarization Failures in Budding Yeast |
title_full_unstemmed | Haspin Modulates the G2/M Transition Delay in Response to Polarization Failures in Budding Yeast |
title_short | Haspin Modulates the G2/M Transition Delay in Response to Polarization Failures in Budding Yeast |
title_sort | haspin modulates the g2/m transition delay in response to polarization failures in budding yeast |
topic | Cell and Developmental Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876276/ https://www.ncbi.nlm.nih.gov/pubmed/33585466 http://dx.doi.org/10.3389/fcell.2020.625717 |
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