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.
引用
收藏
页数:14
相关论文
共 106 条
[1]   Mechanism of processing of the NF-κB2 p100 precursor:: identification of the specific polyubiquitin chain-anchoring lysine residue and analysis of the role of NEDD8-modification on the SCFβ-TrCP ubiquitin ligase [J].
Amir, RE ;
Haecker, H ;
Karin, M ;
Ciechanover, A .
ONCOGENE, 2004, 23 (14) :2540-2547
[2]   A nucleosomal function for IκB kinase-α in NF-κB-dependent gene expression [J].
Anest, V ;
Hanson, JL ;
Cogswell, PC ;
Steinbrecher, KA ;
Strahl, BD ;
Baldwin, AS .
NATURE, 2003, 423 (6940) :659-663
[3]  
BAEUERLE PA, 1994, ANNU REV IMMUNOL, V12, P141, DOI 10.1146/annurev.immunol.12.1.141
[4]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[5]   A fourth IκB protein within the NF-κB signaling module [J].
Basak, Soumen ;
Kim, Hana ;
Kearns, Jeffrey D. ;
Tergaonkar, Vinay ;
O'Dea, Ellen ;
Werner, Shannon L. ;
Benedict, Chris A. ;
Ware, Carl F. ;
Ghosh, Gourisankar ;
Verma, Inder M. ;
Hoffmann, Alexander .
CELL, 2007, 128 (02) :369-381
[6]   EMBRYONIC LETHALITY AND LIVER DEGENERATION IN MICE LACKING THE RELA COMPONENT OF NF-KAPPA-B [J].
BEG, AA ;
SHA, WC ;
BRONSON, RT ;
GHOSH, S ;
BALTIMORE, D .
NATURE, 1995, 376 (6536) :167-170
[7]   THE ONCOPROTEIN BCL-3 DIRECTLY TRANSACTIVATES THROUGH KAPPA-B MOTIFS VIA ASSOCIATION WITH DNA-BINDING P50B HOMODIMERS [J].
BOURS, V ;
FRANZOSO, G ;
AZARENKO, V ;
PARK, S ;
KANNO, T ;
BROWN, K ;
SIEBENLIST, U .
CELL, 1993, 72 (05) :729-739
[8]   In vitro selection of optimal RelB/p52 DNA-binding motifs [J].
Britanova, Liudmila V. ;
Makeev, Vsevolod J. ;
Kuprash, Dmitry V. .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 365 (03) :583-588
[9]   Diverse effects of BCL3 phosphorylation on its modulation of NF-κB p52 homodimer binding to DNA [J].
Bundy, DL ;
McKeithan, TW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (52) :33132-33139
[10]   Negative regulation of Toll-like receptor signaling by NF-κB p50 ubiquitination blockade [J].
Carmody, Ruaidhri J. ;
Ruan, Qingguo ;
Palmer, Scott ;
Hilliard, Brendan ;
Chen, Youhai H. .
SCIENCE, 2007, 317 (5838) :675-678