The Role of Ubiquitin in NF-κB Regulatory Pathways

被引:415
作者
Skaug, Brian [1 ]
Jiang, Xiaomo [1 ]
Chen, Zhijian J. [1 ,2 ]
机构
[1] Univ Texas SW Med Ctr Dallas, Dept Mol Biol, Dallas, TX 75390 USA
[2] Univ Texas SW Med Ctr Dallas, Howard Hughes Med Inst, Dallas, TX 75390 USA
关键词
apoptosis; deubiquitination; IKK; TAK1; TOLL-LIKE-RECEPTOR; NECROSIS-FACTOR-ALPHA; NF-KAPPA-B1 PRECURSOR PROTEIN; DEUBIQUITINATING ENZYME CYLD; ZINC-FINGER PROTEIN; INDUCED CELL-DEATH; CONJUGATING ENZYME; TNF RECEPTOR; SIGNALING PATHWAYS; JNK ACTIVATION;
D O I
10.1146/annurev.biochem.78.070907.102750
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nuclear factor kappa enhancer binding protein (NF-kappa B) regulates diverse biological processes including immunity, inflammation, and apoptosis. A vast array of cellular stimuli converges on NF-kappa B, and ubiquitination plays an essential role in the coordination of these signals to regulate NF-kappa B activity. At least three steps in NF-kappa B activation directly involve ubiquitination: proteasomal degradation of inhibitor of NF-kappa B (I kappa B), processing of NF-kappa B precursors, and activation of the transforming growth factor (TGF)-beta-activated kinase (TAK1) and I kappa B kinase (IKK) complexes. In this review, we discuss recent advances in the identification and characterization of ubiquitination and deubiquitination machinery that regulate NF-kappa B. Particular emphasis is given to proteasome-independent functions of ubiquitin, specifically its role in the activation of protein kinase complexes and in coordination of cell survival and apoptosis signals downstream of tumor necrosis factor alpha (TNF alpha).
引用
收藏
页码:769 / 796
页数:28
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