Signaling to NF- B: Regulation by Ubiquitination
- 7 October 2009
- journal article
- review article
- Published by Cold Spring Harbor Laboratory in Cold Spring Harbor Perspectives in Biology
- Vol. 2 (3), a003350
- https://doi.org/10.1101/cshperspect.a003350
Abstract
The NF-κB pathway is a ubiquitous stress response that activates the NF-κB family of transcription factors. Antigen receptors, receptors of the innate immune system, and certain intracellular stressors are potent activators of this pathway. The transcriptional program that is activated is both antiapoptotic and highly proinflammatory. Indeed, any compromise in engagement of the pathway results in immunodeficiency, whereas constitutive activation generates a sustained inflammatory response that may promote malignancy. As such, NF-κB activation is under tight regulation by a number of post-translational modifications, including phosphorylation and ubiquitination. This article attempts to synthesize our current knowledge regarding the regulation of NF-κB signaling by ubiquitination, specifically highlighting the biochemical basis for both positive and negative feedback loops that function in unison to generate coordinated signals that are essential for the viability of metazoan animals.Keywords
This publication has 90 references indexed in Scilit:
- NOD-like receptors (NLRs): bona fide intracellular microbial sensorsCurrent Opinion in Immunology, 2008
- Multifunctional roles for MALT1 in T-cell activationNature Reviews Immunology, 2008
- From endoplasmic-reticulum stress to the inflammatory responseNature, 2008
- Cutting Edge: K63-Linked Polyubiquitination of NEMO Modulates TLR Signaling and Inflammation In VivoThe Journal of Immunology, 2008
- cIAP1 and cIAP2 Facilitate Cancer Cell Survival by Functioning as E3 Ligases that Promote RIP1 UbiquitinationMolecular Cell, 2008
- Atypical ubiquitin chains: new molecular signalsEMBO Reports, 2008
- (Un)expected roles of c-IAPs in apoptotic and NFκB signaling pathwaysCell Cycle, 2008
- Lys63-Linked Polyubiquitination of IRAK-1 Is Required for Interleukin-1 Receptor- and Toll-Like Receptor-Mediated NF-κB ActivationMolecular and Cellular Biology, 2008
- TIPE2, a Negative Regulator of Innate and Adaptive Immunity that Maintains Immune HomeostasisCell, 2008
- IAPs: What's in a Name?Molecular Cell, 2008