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ERK Signals: Scaffolding Scaffolds?

ERK1/2 MAP Kinases become activated in response to multiple intra- and extra-cellular stimuli through a signaling module composed of sequential tiers of cytoplasmic kinases. Scaffold proteins regulate ERK signals by connecting the different components of the module into a multi-enzymatic complex by...

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Detalles Bibliográficos
Autores principales: Casar, Berta, Crespo, Piero
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885846/
https://www.ncbi.nlm.nih.gov/pubmed/27303664
http://dx.doi.org/10.3389/fcell.2016.00049
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author Casar, Berta
Crespo, Piero
author_facet Casar, Berta
Crespo, Piero
author_sort Casar, Berta
collection PubMed
description ERK1/2 MAP Kinases become activated in response to multiple intra- and extra-cellular stimuli through a signaling module composed of sequential tiers of cytoplasmic kinases. Scaffold proteins regulate ERK signals by connecting the different components of the module into a multi-enzymatic complex by which signal amplitude and duration are fine-tuned, and also provide signal fidelity by isolating this complex from external interferences. In addition, scaffold proteins play a central role as spatial regulators of ERKs signals. In this respect, depending on the subcellular localization from which the activating signals emanate, defined scaffolds specify which substrates are amenable to be phosphorylated. Recent evidence has unveiled direct interactions among different scaffold protein species. These scaffold-scaffold macro-complexes could constitute an additional level of regulation for ERK signals and may serve as nodes for the integration of incoming signals and the subsequent diversification of the outgoing signals with respect to substrate engagement.
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spelling pubmed-48858462016-06-14 ERK Signals: Scaffolding Scaffolds? Casar, Berta Crespo, Piero Front Cell Dev Biol Signaling ERK1/2 MAP Kinases become activated in response to multiple intra- and extra-cellular stimuli through a signaling module composed of sequential tiers of cytoplasmic kinases. Scaffold proteins regulate ERK signals by connecting the different components of the module into a multi-enzymatic complex by which signal amplitude and duration are fine-tuned, and also provide signal fidelity by isolating this complex from external interferences. In addition, scaffold proteins play a central role as spatial regulators of ERKs signals. In this respect, depending on the subcellular localization from which the activating signals emanate, defined scaffolds specify which substrates are amenable to be phosphorylated. Recent evidence has unveiled direct interactions among different scaffold protein species. These scaffold-scaffold macro-complexes could constitute an additional level of regulation for ERK signals and may serve as nodes for the integration of incoming signals and the subsequent diversification of the outgoing signals with respect to substrate engagement. Frontiers Media S.A. 2016-05-31 /pmc/articles/PMC4885846/ /pubmed/27303664 http://dx.doi.org/10.3389/fcell.2016.00049 Text en Copyright © 2016 Casar and Crespo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Signaling
Casar, Berta
Crespo, Piero
ERK Signals: Scaffolding Scaffolds?
title ERK Signals: Scaffolding Scaffolds?
title_full ERK Signals: Scaffolding Scaffolds?
title_fullStr ERK Signals: Scaffolding Scaffolds?
title_full_unstemmed ERK Signals: Scaffolding Scaffolds?
title_short ERK Signals: Scaffolding Scaffolds?
title_sort erk signals: scaffolding scaffolds?
topic Signaling
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4885846/
https://www.ncbi.nlm.nih.gov/pubmed/27303664
http://dx.doi.org/10.3389/fcell.2016.00049
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