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spelling todo:paper_00928674_v160_n6_p1182_Doncic2023-10-03T14:55:22Z Compartmentalization of a bistable switch enables memory to cross a feedback-driven transition Doncic, A. Atay, O. Valk, E. Grande, A. Bush, A. Vasen, G. Colman-Lerner, A. Loog, M. Skotheim, J.M. pheromone CDC24 protein, S cerevisiae cell cycle protein CLN2 protein, S cerevisiae cyclin dependent kinase inhibitor cycline FAR1 protein, S cerevisiae guanine nucleotide exchange factor pheromone Saccharomyces cerevisiae protein Article cell compartmentalization cell cycle G1 phase cell cycle S phase cytoplasm feedback system molecular dynamics nonhuman priority journal protein binding signal transduction cytology feedback system metabolism physiology Saccharomyces cerevisiae Eukaryota Cell Cycle Proteins Cyclin-Dependent Kinase Inhibitor Proteins Cyclins Cytoplasm Feedback, Physiological Guanine Nucleotide Exchange Factors Pheromones Saccharomyces cerevisiae Saccharomyces cerevisiae Proteins Signal Transduction Cells make accurate decisions in the face of molecular noise and environmental fluctuations by relying not only on present pathway activity, but also on their memory of past signaling dynamics. Once a decision is made, cellular transitions are often rapid and switch-like due to positive feedback loops in the regulatory network. While positive feedback loops are good at promoting switch-like transitions, they are not expected to retain information to inform subsequent decisions. However, this expectation is based on our current understanding of network motifs that accounts for temporal, but not spatial, dynamics. Here, we show how spatial organization of the feedback-driven yeast G1/S switch enables the transmission of memory of past pheromone exposure across this transition. We expect this to be one of many examples where the exquisite spatial organization of the eukaryotic cell enables previously well-characterized network motifs to perform new and unexpected signal processing functions. © 2015 Elsevier Inc. JOUR info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by/2.5/ar http://hdl.handle.net/20.500.12110/paper_00928674_v160_n6_p1182_Doncic
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic pheromone
CDC24 protein, S cerevisiae
cell cycle protein
CLN2 protein, S cerevisiae
cyclin dependent kinase inhibitor
cycline
FAR1 protein, S cerevisiae
guanine nucleotide exchange factor
pheromone
Saccharomyces cerevisiae protein
Article
cell compartmentalization
cell cycle G1 phase
cell cycle S phase
cytoplasm
feedback system
molecular dynamics
nonhuman
priority journal
protein binding
signal transduction
cytology
feedback system
metabolism
physiology
Saccharomyces cerevisiae
Eukaryota
Cell Cycle Proteins
Cyclin-Dependent Kinase Inhibitor Proteins
Cyclins
Cytoplasm
Feedback, Physiological
Guanine Nucleotide Exchange Factors
Pheromones
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Signal Transduction
spellingShingle pheromone
CDC24 protein, S cerevisiae
cell cycle protein
CLN2 protein, S cerevisiae
cyclin dependent kinase inhibitor
cycline
FAR1 protein, S cerevisiae
guanine nucleotide exchange factor
pheromone
Saccharomyces cerevisiae protein
Article
cell compartmentalization
cell cycle G1 phase
cell cycle S phase
cytoplasm
feedback system
molecular dynamics
nonhuman
priority journal
protein binding
signal transduction
cytology
feedback system
metabolism
physiology
Saccharomyces cerevisiae
Eukaryota
Cell Cycle Proteins
Cyclin-Dependent Kinase Inhibitor Proteins
Cyclins
Cytoplasm
Feedback, Physiological
Guanine Nucleotide Exchange Factors
Pheromones
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Signal Transduction
Doncic, A.
Atay, O.
Valk, E.
Grande, A.
Bush, A.
Vasen, G.
Colman-Lerner, A.
Loog, M.
Skotheim, J.M.
Compartmentalization of a bistable switch enables memory to cross a feedback-driven transition
topic_facet pheromone
CDC24 protein, S cerevisiae
cell cycle protein
CLN2 protein, S cerevisiae
cyclin dependent kinase inhibitor
cycline
FAR1 protein, S cerevisiae
guanine nucleotide exchange factor
pheromone
Saccharomyces cerevisiae protein
Article
cell compartmentalization
cell cycle G1 phase
cell cycle S phase
cytoplasm
feedback system
molecular dynamics
nonhuman
priority journal
protein binding
signal transduction
cytology
feedback system
metabolism
physiology
Saccharomyces cerevisiae
Eukaryota
Cell Cycle Proteins
Cyclin-Dependent Kinase Inhibitor Proteins
Cyclins
Cytoplasm
Feedback, Physiological
Guanine Nucleotide Exchange Factors
Pheromones
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Signal Transduction
description Cells make accurate decisions in the face of molecular noise and environmental fluctuations by relying not only on present pathway activity, but also on their memory of past signaling dynamics. Once a decision is made, cellular transitions are often rapid and switch-like due to positive feedback loops in the regulatory network. While positive feedback loops are good at promoting switch-like transitions, they are not expected to retain information to inform subsequent decisions. However, this expectation is based on our current understanding of network motifs that accounts for temporal, but not spatial, dynamics. Here, we show how spatial organization of the feedback-driven yeast G1/S switch enables the transmission of memory of past pheromone exposure across this transition. We expect this to be one of many examples where the exquisite spatial organization of the eukaryotic cell enables previously well-characterized network motifs to perform new and unexpected signal processing functions. © 2015 Elsevier Inc.
format JOUR
author Doncic, A.
Atay, O.
Valk, E.
Grande, A.
Bush, A.
Vasen, G.
Colman-Lerner, A.
Loog, M.
Skotheim, J.M.
author_facet Doncic, A.
Atay, O.
Valk, E.
Grande, A.
Bush, A.
Vasen, G.
Colman-Lerner, A.
Loog, M.
Skotheim, J.M.
author_sort Doncic, A.
title Compartmentalization of a bistable switch enables memory to cross a feedback-driven transition
title_short Compartmentalization of a bistable switch enables memory to cross a feedback-driven transition
title_full Compartmentalization of a bistable switch enables memory to cross a feedback-driven transition
title_fullStr Compartmentalization of a bistable switch enables memory to cross a feedback-driven transition
title_full_unstemmed Compartmentalization of a bistable switch enables memory to cross a feedback-driven transition
title_sort compartmentalization of a bistable switch enables memory to cross a feedback-driven transition
url http://hdl.handle.net/20.500.12110/paper_00928674_v160_n6_p1182_Doncic
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AT vaseng compartmentalizationofabistableswitchenablesmemorytocrossafeedbackdriventransition
AT colmanlernera compartmentalizationofabistableswitchenablesmemorytocrossafeedbackdriventransition
AT loogm compartmentalizationofabistableswitchenablesmemorytocrossafeedbackdriventransition
AT skotheimjm compartmentalizationofabistableswitchenablesmemorytocrossafeedbackdriventransition
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