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Molecular mechanisms creating bistable switches at cell cycle transitions
Progression through the eukaryotic cell cycle is characterized by specific transitions, where cells move irreversibly from stage i−1 of the cycle into stage i. These irreversible cell cycle transitions are regulated by underlying bistable switches, which share some common features. An inhibitory pro...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718337/ https://www.ncbi.nlm.nih.gov/pubmed/23486222 http://dx.doi.org/10.1098/rsob.120179 |
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author | Verdugo, Anael Vinod, P. K. Tyson, John J. Novak, Bela |
author_facet | Verdugo, Anael Vinod, P. K. Tyson, John J. Novak, Bela |
author_sort | Verdugo, Anael |
collection | PubMed |
description | Progression through the eukaryotic cell cycle is characterized by specific transitions, where cells move irreversibly from stage i−1 of the cycle into stage i. These irreversible cell cycle transitions are regulated by underlying bistable switches, which share some common features. An inhibitory protein stalls progression, and an activatory protein promotes progression. The inhibitor and activator are locked in a double-negative feedback loop, creating a one-way toggle switch that guarantees an irreversible commitment to move forward through the cell cycle, and it opposes regression from stage i to stage i−1. In many cases, the activator is an enzyme that modifies the inhibitor in multiple steps, whereas the hypo-modified inhibitor binds strongly to the activator and resists its enzymatic activity. These interactions are the basis of a reaction motif that provides a simple and generic account of many characteristic properties of cell cycle transitions. To demonstrate this assertion, we apply the motif in detail to the G1/S transition in budding yeast and to the mitotic checkpoint in mammalian cells. Variations of the motif might support irreversible cellular decision-making in other contexts. |
format | Online Article Text |
id | pubmed-3718337 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-37183372013-07-26 Molecular mechanisms creating bistable switches at cell cycle transitions Verdugo, Anael Vinod, P. K. Tyson, John J. Novak, Bela Open Biol Research Progression through the eukaryotic cell cycle is characterized by specific transitions, where cells move irreversibly from stage i−1 of the cycle into stage i. These irreversible cell cycle transitions are regulated by underlying bistable switches, which share some common features. An inhibitory protein stalls progression, and an activatory protein promotes progression. The inhibitor and activator are locked in a double-negative feedback loop, creating a one-way toggle switch that guarantees an irreversible commitment to move forward through the cell cycle, and it opposes regression from stage i to stage i−1. In many cases, the activator is an enzyme that modifies the inhibitor in multiple steps, whereas the hypo-modified inhibitor binds strongly to the activator and resists its enzymatic activity. These interactions are the basis of a reaction motif that provides a simple and generic account of many characteristic properties of cell cycle transitions. To demonstrate this assertion, we apply the motif in detail to the G1/S transition in budding yeast and to the mitotic checkpoint in mammalian cells. Variations of the motif might support irreversible cellular decision-making in other contexts. The Royal Society 2013-03 /pmc/articles/PMC3718337/ /pubmed/23486222 http://dx.doi.org/10.1098/rsob.120179 Text en http://creativecommons.org/licenses/by/3.0/ © 2013 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Verdugo, Anael Vinod, P. K. Tyson, John J. Novak, Bela Molecular mechanisms creating bistable switches at cell cycle transitions |
title | Molecular mechanisms creating bistable switches at cell cycle transitions |
title_full | Molecular mechanisms creating bistable switches at cell cycle transitions |
title_fullStr | Molecular mechanisms creating bistable switches at cell cycle transitions |
title_full_unstemmed | Molecular mechanisms creating bistable switches at cell cycle transitions |
title_short | Molecular mechanisms creating bistable switches at cell cycle transitions |
title_sort | molecular mechanisms creating bistable switches at cell cycle transitions |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718337/ https://www.ncbi.nlm.nih.gov/pubmed/23486222 http://dx.doi.org/10.1098/rsob.120179 |
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