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...

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Main Authors: Verdugo, A, Vinod, P, Tyson, J, Novak, B
Format: Journal article
Language:English
Published: 2013
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author Verdugo, A
Vinod, P
Tyson, J
Novak, B
author_facet Verdugo, A
Vinod, P
Tyson, J
Novak, B
author_sort Verdugo, A
collection OXFORD
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.
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spelling oxford-uuid:dc87eb8b-8b78-48ec-a1bc-5f83367990c12022-03-27T09:18:26ZMolecular mechanisms creating bistable switches at cell cycle transitions.Journal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:dc87eb8b-8b78-48ec-a1bc-5f83367990c1EnglishSymplectic Elements at Oxford2013Verdugo, AVinod, PTyson, JNovak, BProgression 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.
spellingShingle Verdugo, A
Vinod, P
Tyson, J
Novak, B
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
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AT vinodp molecularmechanismscreatingbistableswitchesatcellcycletransitions
AT tysonj molecularmechanismscreatingbistableswitchesatcellcycletransitions
AT novakb molecularmechanismscreatingbistableswitchesatcellcycletransitions