Signaling to NF-κB: Regulation by Ubiquitination

被引:238
作者
Wertz, Ingrid E. [2 ]
Dixit, Vishva M. [1 ]
机构
[1] Genentech Inc, Dept Physiol Chem, San Francisco, CA 94080 USA
[2] Genentech Inc, Dept Prot Engn, San Francisco, CA 94080 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2010年 / 2卷 / 03期
关键词
TOLL-LIKE-RECEPTOR; T-CELL-ACTIVATION; EDITING ENZYME A20; CONJUGATING ENZYME; TNF-ALPHA; DEUBIQUITINATING ENZYMES; POLYUBIQUITIN BINDING; NEGATIVE REGULATOR; KINASE ACTIVATION; ADAPTIVE IMMUNITY;
D O I
10.1101/cshperspect.a003350
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The NF-kappa B pathway is a ubiquitous stress response that activates the NF-kappa B 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-kappa B 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-kappa B 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.
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页数:19
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