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A theoretical framework for specificity in cell signaling
Different cellular signal transduction pathways are often interconnected, so that the potential for undesirable crosstalk between pathways exists. Nevertheless, signaling networks have evolved that maintain specificity from signal to cellular response. Here, we develop a framework for the analysis o...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1681467/ https://www.ncbi.nlm.nih.gov/pubmed/16729058 http://dx.doi.org/10.1038/msb4100031 |
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author | Komarova, Natalia L Zou, Xiufen Nie, Qing Bardwell, Lee |
author_facet | Komarova, Natalia L Zou, Xiufen Nie, Qing Bardwell, Lee |
author_sort | Komarova, Natalia L |
collection | PubMed |
description | Different cellular signal transduction pathways are often interconnected, so that the potential for undesirable crosstalk between pathways exists. Nevertheless, signaling networks have evolved that maintain specificity from signal to cellular response. Here, we develop a framework for the analysis of networks containing two or more interconnected signaling pathways. We define two properties, specificity and fidelity, that all pathways in a network must possess in order to avoid paradoxical situations where one pathway activates another pathway's output, or responds to another pathway's input, more than its own. In unembellished networks that share components, it is impossible for all pathways to have both mutual specificity and mutual fidelity. However, inclusion of either of two related insulating mechanisms—compartmentalization or the action of a scaffold protein—allows both properties to be achieved, provided deactivation rates are fast compared to exchange rates. |
format | Text |
id | pubmed-1681467 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
record_format | MEDLINE/PubMed |
spelling | pubmed-16814672007-01-25 A theoretical framework for specificity in cell signaling Komarova, Natalia L Zou, Xiufen Nie, Qing Bardwell, Lee Mol Syst Biol Report Different cellular signal transduction pathways are often interconnected, so that the potential for undesirable crosstalk between pathways exists. Nevertheless, signaling networks have evolved that maintain specificity from signal to cellular response. Here, we develop a framework for the analysis of networks containing two or more interconnected signaling pathways. We define two properties, specificity and fidelity, that all pathways in a network must possess in order to avoid paradoxical situations where one pathway activates another pathway's output, or responds to another pathway's input, more than its own. In unembellished networks that share components, it is impossible for all pathways to have both mutual specificity and mutual fidelity. However, inclusion of either of two related insulating mechanisms—compartmentalization or the action of a scaffold protein—allows both properties to be achieved, provided deactivation rates are fast compared to exchange rates. 2005-10-18 /pmc/articles/PMC1681467/ /pubmed/16729058 http://dx.doi.org/10.1038/msb4100031 Text en Copyright © 2005, EMBO and Nature Publishing Group |
spellingShingle | Report Komarova, Natalia L Zou, Xiufen Nie, Qing Bardwell, Lee A theoretical framework for specificity in cell signaling |
title | A theoretical framework for specificity in cell signaling |
title_full | A theoretical framework for specificity in cell signaling |
title_fullStr | A theoretical framework for specificity in cell signaling |
title_full_unstemmed | A theoretical framework for specificity in cell signaling |
title_short | A theoretical framework for specificity in cell signaling |
title_sort | theoretical framework for specificity in cell signaling |
topic | Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1681467/ https://www.ncbi.nlm.nih.gov/pubmed/16729058 http://dx.doi.org/10.1038/msb4100031 |
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