Charting the NF-κB pathway interactome map.

Inflammation is part of a complex physiological response to harmful stimuli and pathogenic stress. The five components of the Nuclear Factor κB (NF-κB) family are prominent mediators of inflammation, acting as key transcriptional regulators of hundreds of genes. Several signaling pathways activated...

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Main Authors: Paolo Tieri, Alberto Termanini, Elena Bellavista, Stefano Salvioli, Miriam Capri, Claudio Franceschi
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3293857?pdf=render
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spelling doaj-baa0212e6fc343ef883e0cef425fbcec2020-11-25T01:45:55ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-0173e3267810.1371/journal.pone.0032678Charting the NF-κB pathway interactome map.Paolo TieriAlberto TermaniniElena BellavistaStefano SalvioliMiriam CapriClaudio FranceschiInflammation is part of a complex physiological response to harmful stimuli and pathogenic stress. The five components of the Nuclear Factor κB (NF-κB) family are prominent mediators of inflammation, acting as key transcriptional regulators of hundreds of genes. Several signaling pathways activated by diverse stimuli converge on NF-κB activation, resulting in a regulatory system characterized by high complexity. It is increasingly recognized that the number of components that impinges upon phenotypic outcomes of signal transduction pathways may be higher than those taken into consideration from canonical pathway representations. Scope of the present analysis is to provide a wider, systemic picture of the NF-κB signaling system. Data from different sources such as literature, functional enrichment web resources, protein-protein interaction and pathway databases have been gathered, curated, integrated and analyzed in order to reconstruct a single, comprehensive picture of the proteins that interact with, and participate to the NF-κB activation system. Such a reconstruction shows that the NF-κB interactome is substantially different in quantity and quality of components with respect to canonical representations. The analysis highlights that several neglected but topologically central proteins may play a role in the activation of NF-κB mediated responses. Moreover the interactome structure fits with the characteristics of a bow tie architecture. This interactome is intended as an open network resource available for further development, refinement and analysis.http://europepmc.org/articles/PMC3293857?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Paolo Tieri
Alberto Termanini
Elena Bellavista
Stefano Salvioli
Miriam Capri
Claudio Franceschi
spellingShingle Paolo Tieri
Alberto Termanini
Elena Bellavista
Stefano Salvioli
Miriam Capri
Claudio Franceschi
Charting the NF-κB pathway interactome map.
PLoS ONE
author_facet Paolo Tieri
Alberto Termanini
Elena Bellavista
Stefano Salvioli
Miriam Capri
Claudio Franceschi
author_sort Paolo Tieri
title Charting the NF-κB pathway interactome map.
title_short Charting the NF-κB pathway interactome map.
title_full Charting the NF-κB pathway interactome map.
title_fullStr Charting the NF-κB pathway interactome map.
title_full_unstemmed Charting the NF-κB pathway interactome map.
title_sort charting the nf-κb pathway interactome map.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2012-01-01
description Inflammation is part of a complex physiological response to harmful stimuli and pathogenic stress. The five components of the Nuclear Factor κB (NF-κB) family are prominent mediators of inflammation, acting as key transcriptional regulators of hundreds of genes. Several signaling pathways activated by diverse stimuli converge on NF-κB activation, resulting in a regulatory system characterized by high complexity. It is increasingly recognized that the number of components that impinges upon phenotypic outcomes of signal transduction pathways may be higher than those taken into consideration from canonical pathway representations. Scope of the present analysis is to provide a wider, systemic picture of the NF-κB signaling system. Data from different sources such as literature, functional enrichment web resources, protein-protein interaction and pathway databases have been gathered, curated, integrated and analyzed in order to reconstruct a single, comprehensive picture of the proteins that interact with, and participate to the NF-κB activation system. Such a reconstruction shows that the NF-κB interactome is substantially different in quantity and quality of components with respect to canonical representations. The analysis highlights that several neglected but topologically central proteins may play a role in the activation of NF-κB mediated responses. Moreover the interactome structure fits with the characteristics of a bow tie architecture. This interactome is intended as an open network resource available for further development, refinement and analysis.
url http://europepmc.org/articles/PMC3293857?pdf=render
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