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Phase-Locked Signals Elucidate Circuit Architecture of an Oscillatory Pathway

This paper introduces the concept of phase-locking analysis of oscillatory cellular signaling systems to elucidate biochemical circuit architecture. Phase-locking is a physical phenomenon that refers to a response mode in which system output is synchronized to a periodic stimulus; in some instances,...

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Autores principales: Jovic, Andreja, Howell, Bryan, Cote, Michelle, Wade, Susan M., Mehta, Khamir, Miyawaki, Atsushi, Neubig, Richard R., Linderman, Jennifer J., Takayama, Shuichi
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009597/
https://www.ncbi.nlm.nih.gov/pubmed/21203481
http://dx.doi.org/10.1371/journal.pcbi.1001040
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author Jovic, Andreja
Howell, Bryan
Cote, Michelle
Wade, Susan M.
Mehta, Khamir
Miyawaki, Atsushi
Neubig, Richard R.
Linderman, Jennifer J.
Takayama, Shuichi
author_facet Jovic, Andreja
Howell, Bryan
Cote, Michelle
Wade, Susan M.
Mehta, Khamir
Miyawaki, Atsushi
Neubig, Richard R.
Linderman, Jennifer J.
Takayama, Shuichi
author_sort Jovic, Andreja
collection PubMed
description This paper introduces the concept of phase-locking analysis of oscillatory cellular signaling systems to elucidate biochemical circuit architecture. Phase-locking is a physical phenomenon that refers to a response mode in which system output is synchronized to a periodic stimulus; in some instances, the number of responses can be fewer than the number of inputs, indicative of skipped beats. While the observation of phase-locking alone is largely independent of detailed mechanism, we find that the properties of phase-locking are useful for discriminating circuit architectures because they reflect not only the activation but also the recovery characteristics of biochemical circuits. Here, this principle is demonstrated for analysis of a G-protein coupled receptor system, the M3 muscarinic receptor-calcium signaling pathway, using microfluidic-mediated periodic chemical stimulation of the M3 receptor with carbachol and real-time imaging of resulting calcium transients. Using this approach we uncovered the potential importance of basal IP3 production, a finding that has important implications on calcium response fidelity to periodic stimulation. Based upon our analysis, we also negated the notion that the Gq-PLC interaction is switch-like, which has a strong influence upon how extracellular signals are filtered and interpreted downstream. Phase-locking analysis is a new and useful tool for model revision and mechanism elucidation; the method complements conventional genetic and chemical tools for analysis of cellular signaling circuitry and should be broadly applicable to other oscillatory pathways.
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spelling pubmed-30095972011-01-03 Phase-Locked Signals Elucidate Circuit Architecture of an Oscillatory Pathway Jovic, Andreja Howell, Bryan Cote, Michelle Wade, Susan M. Mehta, Khamir Miyawaki, Atsushi Neubig, Richard R. Linderman, Jennifer J. Takayama, Shuichi PLoS Comput Biol Research Article This paper introduces the concept of phase-locking analysis of oscillatory cellular signaling systems to elucidate biochemical circuit architecture. Phase-locking is a physical phenomenon that refers to a response mode in which system output is synchronized to a periodic stimulus; in some instances, the number of responses can be fewer than the number of inputs, indicative of skipped beats. While the observation of phase-locking alone is largely independent of detailed mechanism, we find that the properties of phase-locking are useful for discriminating circuit architectures because they reflect not only the activation but also the recovery characteristics of biochemical circuits. Here, this principle is demonstrated for analysis of a G-protein coupled receptor system, the M3 muscarinic receptor-calcium signaling pathway, using microfluidic-mediated periodic chemical stimulation of the M3 receptor with carbachol and real-time imaging of resulting calcium transients. Using this approach we uncovered the potential importance of basal IP3 production, a finding that has important implications on calcium response fidelity to periodic stimulation. Based upon our analysis, we also negated the notion that the Gq-PLC interaction is switch-like, which has a strong influence upon how extracellular signals are filtered and interpreted downstream. Phase-locking analysis is a new and useful tool for model revision and mechanism elucidation; the method complements conventional genetic and chemical tools for analysis of cellular signaling circuitry and should be broadly applicable to other oscillatory pathways. Public Library of Science 2010-12-23 /pmc/articles/PMC3009597/ /pubmed/21203481 http://dx.doi.org/10.1371/journal.pcbi.1001040 Text en Jovic et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Jovic, Andreja
Howell, Bryan
Cote, Michelle
Wade, Susan M.
Mehta, Khamir
Miyawaki, Atsushi
Neubig, Richard R.
Linderman, Jennifer J.
Takayama, Shuichi
Phase-Locked Signals Elucidate Circuit Architecture of an Oscillatory Pathway
title Phase-Locked Signals Elucidate Circuit Architecture of an Oscillatory Pathway
title_full Phase-Locked Signals Elucidate Circuit Architecture of an Oscillatory Pathway
title_fullStr Phase-Locked Signals Elucidate Circuit Architecture of an Oscillatory Pathway
title_full_unstemmed Phase-Locked Signals Elucidate Circuit Architecture of an Oscillatory Pathway
title_short Phase-Locked Signals Elucidate Circuit Architecture of an Oscillatory Pathway
title_sort phase-locked signals elucidate circuit architecture of an oscillatory pathway
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009597/
https://www.ncbi.nlm.nih.gov/pubmed/21203481
http://dx.doi.org/10.1371/journal.pcbi.1001040
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