Molecular mechanisms creating bistable switches at cell cycle transitions
dc.contributor.author | Verdugo, Anael | en |
dc.contributor.author | Vinod, P. K. | en |
dc.contributor.author | Tyson, John J. | en |
dc.contributor.author | Novak, Bela | en |
dc.contributor.department | Biological Sciences | en |
dc.date.accessioned | 2016-12-09T21:40:52Z | en |
dc.date.available | 2016-12-09T21:40:52Z | en |
dc.date.issued | 2013-03-01 | en |
dc.description.abstract | Progression through the eukaryotic cell cycle is characterized by specific transitions, where cells move irreversibly from stage i 21 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 2 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. | en |
dc.description.version | Published version | en |
dc.format.extent | 14 pages | en |
dc.format.mimetype | application/pdf | en |
dc.identifier.doi | https://doi.org/10.1098/rsob.120179 | en |
dc.identifier.issn | 2046-2441 | en |
dc.identifier.uri | http://hdl.handle.net/10919/73642 | en |
dc.identifier.volume | 3 | en |
dc.language.iso | en | en |
dc.publisher | Royal Society | en |
dc.relation.uri | http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000318268500002&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=930d57c9ac61a043676db62af60056c1 | en |
dc.rights | Creative Commons Attribution 3.0 Unported | en |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/ | en |
dc.subject | Biochemistry & Molecular Biology | en |
dc.subject | cell cycle | en |
dc.subject | checkpoints | en |
dc.subject | bistability | en |
dc.subject | network motifs | en |
dc.subject | SPINDLE-ASSEMBLY CHECKPOINT | en |
dc.subject | SYSTEMS-LEVEL FEEDBACK | en |
dc.subject | MULTISITE PHOSPHORYLATION | en |
dc.subject | SACCHAROMYCES-CEREVISIAE | en |
dc.subject | RESTRICTION POINT | en |
dc.subject | ANAPHASE SWITCH | en |
dc.subject | MITOTIC ARREST | en |
dc.subject | CDK INHIBITOR | en |
dc.subject | S PHASE | en |
dc.subject | DESTRUCTION | en |
dc.title | Molecular mechanisms creating bistable switches at cell cycle transitions | en |
dc.title.serial | Open Biology | en |
dc.type | Article - Refereed | en |
dc.type.dcmitype | Text | en |
pubs.organisational-group | /Virginia Tech | en |
pubs.organisational-group | /Virginia Tech/All T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/Faculty of Health Sciences | en |
pubs.organisational-group | /Virginia Tech/Science | en |
pubs.organisational-group | /Virginia Tech/Science/Biological Sciences | en |
pubs.organisational-group | /Virginia Tech/Science/COS T&R Faculty | en |
pubs.organisational-group | /Virginia Tech/University Distinguished Professors | en |
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