Cargando…
Cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches
The start-transition (START) in the G1 phase marks the point in the cell cycle at which a yeast cell initiates a new round of cell division. Once made, this decision is irreversible and the cell is committed to progressing through the entire cell cycle, irrespective of arrest signals such as pheromo...
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352082/ https://www.ncbi.nlm.nih.gov/pubmed/22645649 http://dx.doi.org/10.1098/rsob.110009 |
_version_ | 1782232844052987904 |
---|---|
author | Zhang, Tongli Schmierer, Bernhard Novák, Béla |
author_facet | Zhang, Tongli Schmierer, Bernhard Novák, Béla |
author_sort | Zhang, Tongli |
collection | PubMed |
description | The start-transition (START) in the G1 phase marks the point in the cell cycle at which a yeast cell initiates a new round of cell division. Once made, this decision is irreversible and the cell is committed to progressing through the entire cell cycle, irrespective of arrest signals such as pheromone. How commitment emerges from the underlying molecular interaction network is poorly understood. Here, we perform a dynamical systems analysis of an established cell cycle model, which has never been analysed from a commitment perspective. We show that the irreversibility of the START transition and subsequent commitment can be consistently explained in terms of the interplay of multiple bistable molecular switches. By applying an existing mathematical model to a novel problem and by expanding the model in a self-consistent manner, we achieve several goals: we bring together a large number of experimental findings into a coherent theoretical framework; we increase the scope and the applicability of the original model; we give a systems level explanation of how the START transition and the cell cycle commitment arise from the dynamical features of the underlying molecular interaction network; and we make clear, experimentally testable predictions. |
format | Online Article Text |
id | pubmed-3352082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-33520822012-05-29 Cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches Zhang, Tongli Schmierer, Bernhard Novák, Béla Open Biol Research The start-transition (START) in the G1 phase marks the point in the cell cycle at which a yeast cell initiates a new round of cell division. Once made, this decision is irreversible and the cell is committed to progressing through the entire cell cycle, irrespective of arrest signals such as pheromone. How commitment emerges from the underlying molecular interaction network is poorly understood. Here, we perform a dynamical systems analysis of an established cell cycle model, which has never been analysed from a commitment perspective. We show that the irreversibility of the START transition and subsequent commitment can be consistently explained in terms of the interplay of multiple bistable molecular switches. By applying an existing mathematical model to a novel problem and by expanding the model in a self-consistent manner, we achieve several goals: we bring together a large number of experimental findings into a coherent theoretical framework; we increase the scope and the applicability of the original model; we give a systems level explanation of how the START transition and the cell cycle commitment arise from the dynamical features of the underlying molecular interaction network; and we make clear, experimentally testable predictions. The Royal Society 2011-11 /pmc/articles/PMC3352082/ /pubmed/22645649 http://dx.doi.org/10.1098/rsob.110009 Text en http://creativecommons.org/licenses/by/3.0/ © 2011 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 Zhang, Tongli Schmierer, Bernhard Novák, Béla Cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches |
title | Cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches |
title_full | Cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches |
title_fullStr | Cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches |
title_full_unstemmed | Cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches |
title_short | Cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches |
title_sort | cell cycle commitment in budding yeast emerges from the cooperation of multiple bistable switches |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3352082/ https://www.ncbi.nlm.nih.gov/pubmed/22645649 http://dx.doi.org/10.1098/rsob.110009 |
work_keys_str_mv | AT zhangtongli cellcyclecommitmentinbuddingyeastemergesfromthecooperationofmultiplebistableswitches AT schmiererbernhard cellcyclecommitmentinbuddingyeastemergesfromthecooperationofmultiplebistableswitches AT novakbela cellcyclecommitmentinbuddingyeastemergesfromthecooperationofmultiplebistableswitches |