Signal response sensitivity in the yeast mitogen-activated protein kinase cascade.

The yeast pheromone response pathway is a canonical three-step mitogen activated protein kinase (MAPK) cascade which requires a scaffold protein for proper signal transduction. Recent experimental studies into the role the scaffold plays in modulating the character of the transduced signal, show tha...

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Main Authors: Craig J Thalhauser, Natalia L Komarova
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2010-07-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC2909145?pdf=render
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spelling doaj-8073cbf136c24717a1f96daaa8e1f7ef2020-11-25T01:23:38ZengPublic Library of Science (PLoS)PLoS ONE1932-62032010-07-0157e1156810.1371/journal.pone.0011568Signal response sensitivity in the yeast mitogen-activated protein kinase cascade.Craig J ThalhauserNatalia L KomarovaThe yeast pheromone response pathway is a canonical three-step mitogen activated protein kinase (MAPK) cascade which requires a scaffold protein for proper signal transduction. Recent experimental studies into the role the scaffold plays in modulating the character of the transduced signal, show that the presence of the scaffold increases the biphasic nature of the signal response. This runs contrary to prior theoretical investigations into how scaffolds function. We describe a mathematical model of the yeast MAPK cascade specifically designed to capture the experimental conditions and results of these empirical studies. We demonstrate how the system can exhibit either graded or ultrasensitive (biphasic) response dynamics based on the binding kinetics of enzymes to the scaffold. At the basis of our theory is an analytical result that weak interactions make the response biphasic while tight interactions lead to a graded response. We then show via an analysis of the kinetic binding rate constants how the results of experimental manipulations, modeled as changes to certain of these binding constants, lead to predictions of pathway output consistent with experimental observations. We demonstrate how the results of these experimental manipulations are consistent within the framework of our theoretical treatment of this scaffold-dependent MAPK cascades, and how future efforts in this style of systems biology can be used to interpret the results of other signal transduction observations.http://europepmc.org/articles/PMC2909145?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Craig J Thalhauser
Natalia L Komarova
spellingShingle Craig J Thalhauser
Natalia L Komarova
Signal response sensitivity in the yeast mitogen-activated protein kinase cascade.
PLoS ONE
author_facet Craig J Thalhauser
Natalia L Komarova
author_sort Craig J Thalhauser
title Signal response sensitivity in the yeast mitogen-activated protein kinase cascade.
title_short Signal response sensitivity in the yeast mitogen-activated protein kinase cascade.
title_full Signal response sensitivity in the yeast mitogen-activated protein kinase cascade.
title_fullStr Signal response sensitivity in the yeast mitogen-activated protein kinase cascade.
title_full_unstemmed Signal response sensitivity in the yeast mitogen-activated protein kinase cascade.
title_sort signal response sensitivity in the yeast mitogen-activated protein kinase cascade.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2010-07-01
description The yeast pheromone response pathway is a canonical three-step mitogen activated protein kinase (MAPK) cascade which requires a scaffold protein for proper signal transduction. Recent experimental studies into the role the scaffold plays in modulating the character of the transduced signal, show that the presence of the scaffold increases the biphasic nature of the signal response. This runs contrary to prior theoretical investigations into how scaffolds function. We describe a mathematical model of the yeast MAPK cascade specifically designed to capture the experimental conditions and results of these empirical studies. We demonstrate how the system can exhibit either graded or ultrasensitive (biphasic) response dynamics based on the binding kinetics of enzymes to the scaffold. At the basis of our theory is an analytical result that weak interactions make the response biphasic while tight interactions lead to a graded response. We then show via an analysis of the kinetic binding rate constants how the results of experimental manipulations, modeled as changes to certain of these binding constants, lead to predictions of pathway output consistent with experimental observations. We demonstrate how the results of these experimental manipulations are consistent within the framework of our theoretical treatment of this scaffold-dependent MAPK cascades, and how future efforts in this style of systems biology can be used to interpret the results of other signal transduction observations.
url http://europepmc.org/articles/PMC2909145?pdf=render
work_keys_str_mv AT craigjthalhauser signalresponsesensitivityintheyeastmitogenactivatedproteinkinasecascade
AT natalialkomarova signalresponsesensitivityintheyeastmitogenactivatedproteinkinasecascade
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