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Prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis
We investigated how Saccharomyces cerevisiae coordinate polarization, budding, and anaphase during a unique developmental program called return to growth (RTG) in which cells in meiosis return to mitosis upon nutrient shift. Cells reentering mitosis from prophase I deviate from the normal cell cycle...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Rockefeller University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028541/ https://www.ncbi.nlm.nih.gov/pubmed/29743192 http://dx.doi.org/10.1083/jcb.201708153 |
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author | Gihana, Gabriel M. Musser, Tiffany R. Thompson, Oscar Lacefield, Soni |
author_facet | Gihana, Gabriel M. Musser, Tiffany R. Thompson, Oscar Lacefield, Soni |
author_sort | Gihana, Gabriel M. |
collection | PubMed |
description | We investigated how Saccharomyces cerevisiae coordinate polarization, budding, and anaphase during a unique developmental program called return to growth (RTG) in which cells in meiosis return to mitosis upon nutrient shift. Cells reentering mitosis from prophase I deviate from the normal cell cycle by budding in G2 instead of G1. We found that cells do not maintain the bipolar budding pattern, a characteristic of diploid cells. Furthermore, strict temporal regulation of M-phase cyclin-dependent kinase (CDK; M-CDK) is important for polarity establishment and morphogenesis. Cells with premature M-CDK activity caused by loss of checkpoint kinase Swe1 failed to polarize and underwent anaphase without budding. Mutants with increased Swe1-dependent M-CDK inhibition showed additional or more penetrant phenotypes in RTG than mitosis, including elongated buds, multiple buds, spindle mispositioning, and septin perturbation. Surprisingly, the enhanced and additional phenotypes were not exclusive to RTG but also occurred with prolonged Swe1-dependent CDK inhibition in mitosis. Our analysis reveals that prolonged activation of the Swe1-dependent checkpoint can be detrimental instead of beneficial. |
format | Online Article Text |
id | pubmed-6028541 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-60285412019-01-02 Prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis Gihana, Gabriel M. Musser, Tiffany R. Thompson, Oscar Lacefield, Soni J Cell Biol Research Articles We investigated how Saccharomyces cerevisiae coordinate polarization, budding, and anaphase during a unique developmental program called return to growth (RTG) in which cells in meiosis return to mitosis upon nutrient shift. Cells reentering mitosis from prophase I deviate from the normal cell cycle by budding in G2 instead of G1. We found that cells do not maintain the bipolar budding pattern, a characteristic of diploid cells. Furthermore, strict temporal regulation of M-phase cyclin-dependent kinase (CDK; M-CDK) is important for polarity establishment and morphogenesis. Cells with premature M-CDK activity caused by loss of checkpoint kinase Swe1 failed to polarize and underwent anaphase without budding. Mutants with increased Swe1-dependent M-CDK inhibition showed additional or more penetrant phenotypes in RTG than mitosis, including elongated buds, multiple buds, spindle mispositioning, and septin perturbation. Surprisingly, the enhanced and additional phenotypes were not exclusive to RTG but also occurred with prolonged Swe1-dependent CDK inhibition in mitosis. Our analysis reveals that prolonged activation of the Swe1-dependent checkpoint can be detrimental instead of beneficial. Rockefeller University Press 2018-07-02 /pmc/articles/PMC6028541/ /pubmed/29743192 http://dx.doi.org/10.1083/jcb.201708153 Text en © 2018 Gihana et al. http://www.rupress.org/terms/https://creativecommons.org/licenses/by-nc-sa/4.0/This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms/). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Research Articles Gihana, Gabriel M. Musser, Tiffany R. Thompson, Oscar Lacefield, Soni Prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis |
title | Prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis |
title_full | Prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis |
title_fullStr | Prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis |
title_full_unstemmed | Prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis |
title_short | Prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis |
title_sort | prolonged cyclin-dependent kinase inhibition results in septin perturbations during return to growth and mitosis |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028541/ https://www.ncbi.nlm.nih.gov/pubmed/29743192 http://dx.doi.org/10.1083/jcb.201708153 |
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