Post-translational modifications regulating the activity and function of the nuclear factor kappa B pathway

被引:568
作者
Perkins, N. D. [1 ]
机构
[1] Univ Dundee, Sch Life Sci, Div Gene Regulat & Express, Dundee DD1 5EH, Scotland
基金
英国惠康基金;
关键词
NF-kappa B; IKK; I kappa B; phosphorylation; ubiquitination; modification;
D O I
10.1038/sj.onc.1209937
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
The diverse cellular and biological functions of the nuclear factor kappa B (NF-kappa B) pathway, together with the catastrophic consequences of its aberrant regulation, demand specific and highly regulated control of its activity. As described in this review, regulation of the NF-kappa B pathway is brought about through multiple post-translational modi. cations that control the activity of the core components of NF-kappa B signaling: the I kappa B kinase (IKK) complex, the I kappa B proteins and the NF-kappa B subunits themselves. These regulatory modi. cations, which include phosphorylation, ubiquitination, acetylation, sumoylation and nitrosylation, can vary, depending on the nature of the NF-kappa B-inducing stimulus. Moreover, they frequently have distinct, sometimes antagonistic, functional consequences and the same modi. cation can have different effects depending on the context. Given the important role of NF-kappa B in human health and disease, understanding these pathways will not only provide valuable insights into mechanism and function, but could also lead to new drug targets and the development of diagnostic and prognostic biomarkers for many pathological conditions.
引用
收藏
页码:6717 / 6730
页数:14
相关论文
共 141 条
[11]   Constitutive and interleukin-1-inducible phosphorylation of p65 NF-κB at serine 536 is mediated by multiple protein kinases including IκB kinase (IKK)-α, IKKβ, IKKε, TRAF family member-associated (TANK)-binding kinase 1 (TBK1), and an unknown kinase and couples p65 to TATA-binding protein-associated factor II31-mediated interleukin-8 transcription [J].
Buss, H ;
Dörrie, A ;
Schmitz, ML ;
Hoffmann, E ;
Resch, K ;
Kracht, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (53) :55633-55643
[12]   Phosphorylation of serine 468 by GSK-3β negatively regulates basal p65 NF-κB activity [J].
Buss, H ;
Dörrie, A ;
Schmitz, ML ;
Frank, R ;
Livingstone, M ;
Resch, K ;
Kracht, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (48) :49571-49574
[13]   Cisplatin mimics ARF tumor suppressor regulation of RelA (p65) nuclear factor-κB transactivation [J].
Campbell, KJ ;
Witty, JM ;
Rocha, S ;
Perkins, ND .
CANCER RESEARCH, 2006, 66 (02) :929-935
[14]   Site-specific monoubiquitination of IκB kinase IKKβ regulates its phosphorylation and persistent activation [J].
Carter, RS ;
Pennington, KN ;
Arrate, P ;
Oltz, EM ;
Ballard, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (52) :43272-43279
[15]   In vivo identification of inducible phosphoacceptors in the IKKγ/NEMO subunit of human IκB kinase [J].
Carter, RS ;
Pennington, KN ;
Ungurait, BJ ;
Ballard, DW .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (22) :19642-19648
[16]   Degradation of proto-oncoprotein c-Rel by the ubiquitin-proteasome pathway [J].
Chen, E ;
Hrdlickova, R ;
Nehyba, J ;
Longo, DL ;
Bose, HR ;
Li, CCH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (52) :35201-35207
[17]   Shaping the nuclear action of NF-κB [J].
Chen, LF ;
Greene, WC .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2004, 5 (05) :392-401
[18]   Acetylation of ReIA at discrete sites regulates distinct nuclear functions of NF-κB [J].
Chen, LF ;
Mu, YJ ;
Greene, WC .
EMBO JOURNAL, 2002, 21 (23) :6539-6548
[19]   NF-κB RelA phosphorylation regulates RelA acetylation [J].
Chen, LF ;
Williams, SA ;
Mu, YJ ;
Nakano, H ;
Duerr, JM ;
Buckbinder, L ;
Greene, WC .
MOLECULAR AND CELLULAR BIOLOGY, 2005, 25 (18) :7966-7975
[20]   Ubiquitin, TAK1 and IKK: is there a connection? [J].
Chen, ZJ ;
Bhoj, V ;
Seth, RB .
CELL DEATH AND DIFFERENTIATION, 2006, 13 (05) :687-692