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绘制 NF-κB 通路互作图谱。

Charting the NF-κB pathway interactome map.

机构信息

CIG Luigi Galvani Interdept Center, University of Bologna, Bologna, Italy.

出版信息

PLoS One. 2012;7(3):e32678. doi: 10.1371/journal.pone.0032678. Epub 2012 Mar 5.

DOI:10.1371/journal.pone.0032678
PMID:22403694
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3293857/
Abstract

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.

摘要

炎症是对有害刺激和致病应激的复杂生理反应的一部分。核因子 kappa B(NF-κB)家族的五个成分是炎症的主要介质,作为数百个基因的关键转录调节因子发挥作用。多种刺激激活的几条信号通路汇集到 NF-κB 的激活,导致一个以高度复杂性为特征的调节系统。人们越来越认识到,影响信号转导途径表型结果的组件数量可能高于从经典途径表示中考虑的数量。本分析的范围是提供 NF-κB 信号系统更广泛、系统的图片。从文献、功能富集网络资源、蛋白质-蛋白质相互作用和途径数据库等不同来源收集、整理、整合和分析数据,以便重建与 NF-κB 激活系统相互作用和参与的蛋白质的单一、综合图片。这种重建表明,与经典表示相比,NF-κB 相互作用组在数量和质量上的成分有很大的不同。该分析强调了几个被忽视但拓扑中心的蛋白质可能在 NF-κB 介导的反应的激活中发挥作用。此外,相互作用组的结构与蝴蝶结结构的特征相吻合。该相互作用组旨在作为一个开放的网络资源,可用于进一步的开发、改进和分析。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c67b/3293857/9820d242b89b/pone.0032678.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c67b/3293857/f0840b17f5bd/pone.0032678.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c67b/3293857/0e9c4ab44acc/pone.0032678.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c67b/3293857/9820d242b89b/pone.0032678.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c67b/3293857/f0840b17f5bd/pone.0032678.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c67b/3293857/0e9c4ab44acc/pone.0032678.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c67b/3293857/9820d242b89b/pone.0032678.g003.jpg

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