The NF-κB Family of Transcription Factors and Its Regulation

被引:2098
作者
Oeckinghaus, Andrea [1 ,2 ,3 ]
Ghosh, Sankar [1 ,2 ,3 ]
机构
[1] Yale Univ, Dept Immunobiol, Sch Med, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Mol Biophys & Biochem, New Haven, CT 06520 USA
[3] Columbia Univ, Coll Phys & Surg, Dept Microbiol & Immunol, New York, NY 10032 USA
来源
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY | 2009年 / 1卷 / 04期
关键词
INDUCIBLE NUCLEAR-PROTEIN; IKK-ALPHA; GENE-EXPRESSION; KINASE-ALPHA; BETA-TRCP; DEPENDENT DEGRADATION; CRYSTAL-STRUCTURE; SIGNALING MODULE; UBIQUITIN LIGASE; DNA-BINDING;
D O I
10.1101/cshperspect.a000034
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Nuclear factor-kappa B (NF-kappa B) consists of a family of transcription factors that play critical roles in inflammation, immunity, cell proliferation, differentiation, and survival. Inducible NF-kappa B activation depends on phosphorylation-induced proteosomal degradation of the inhibitor of NF-kappa B proteins (I kappa Bs), which retain inactive NF-kappa B dimers in the cytosol in unstimulated cells. The majority of the diverse signaling pathways that lead to NF-kappa B activation converge on the I kappa B kinase (IKK) complex, which is responsible for I kappa B phosphorylation and is essential for signal transduction to NF-kappa B. Additional regulation of NF-kappa B activity is achieved through various post-translational modifications of the core components of the NF-kappa B signaling pathways. In addition to cytosolic modifications of IKK and I kappa B proteins, as well as other pathway-specific mediators, the transcription factors are themselves extensively modified. Tremendous progress has been made over the last two decades in unraveling the elaborate regulatory networks that control the NF-kappa B response. This has made the NF-kappa B pathway a paradigm for understanding general principles of signal transduction and gene regulation.
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页数:14
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共 106 条
[101]   Identification of the receptor component of the IκBα-ubiquitin ligase [J].
Yaron, A ;
Hatzubai, A ;
Davis, M ;
Lavon, I ;
Amit, S ;
Manning, AM ;
Andersen, JS ;
Mann, M ;
Mercurio, F ;
Ben-Neriah, Y .
NATURE, 1998, 396 (6711) :590-594
[102]   Modulation of NF-κB-dependent transcription and cell survival by the SIRT1 deacetylase [J].
Yeung, F ;
Hoberg, JE ;
Ramsey, CS ;
Keller, MD ;
Jones, DR ;
Frye, RA ;
Mayo, MW .
EMBO JOURNAL, 2004, 23 (12) :2369-2380
[103]   The I kappa B kinase complex (IKK) contains two kinase subunits, IKK alpha and IKK beta, necessary for I kappa B phosphorylation and NF-kappa B activation [J].
Zandi, E ;
Rothwarf, DM ;
Delhase, M ;
Hayakawa, M ;
Karin, M .
CELL, 1997, 91 (02) :243-252
[104]   Direct phosphorylation of IκB by IKKα and IKKβ:: Discrimination between free and NF-κB-bound substrate [J].
Zandi, E ;
Chen, Y ;
Karin, M .
SCIENCE, 1998, 281 (5381) :1360-1363
[105]   Phosphorylation of NF-κB p65 by PKA stimulates transcriptional activity by promoting a novel bivalent interaction with the coactivator CBP/p300 [J].
Zhong, HH ;
Voll, RE ;
Ghosh, S .
MOLECULAR CELL, 1998, 1 (05) :661-671
[106]   The phosphorylation status of nuclear NF-κB determines its association with CBP/p300 or HDAC-1 [J].
Zhong, HH ;
May, MJ ;
Jimi, E ;
Ghosh, S .
MOLECULAR CELL, 2002, 9 (03) :625-636