COMMD proteins, a novel family of structural and functional homologs of MURR1

被引:223
作者
Burstein, E
Hoberg, JE
Wilkinson, AS
Rumble, JM
Csomos, RA
Komarck, CM
Maine, GN
Wilkinson, JC
Mayo, MW
Duckett, CS
机构
[1] Univ Michigan, Sch Med, Dept Internal Med, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Sch Med, Dept Pathol, Ann Arbor, MI 48109 USA
[3] Univ Virginia, Dept Mol Genet & Biochem, Charlottesville, VA 22908 USA
[4] Ann Arbor Vet Affairs MEd Ctr, Gastroenterol Sect, Ann Arbor, MI 48105 USA
关键词
D O I
10.1074/jbc.M501928200
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
MURR1 is a multifunctional protein that inhibits nuclear factor kB (NF-kB), a transcription factor with pleiotropic functions affecting innate and adaptive immunity, apoptosis, cell cycle regulation, and oncogenesis. Here we report the discovery of a new family of proteins with homology to MURR1. These proteins form multimeric complexes and were identified in a biochemical screen for MURR1-associated factors. The family is defined by the presence of a conserved and unique motif termed the COMM ( copper metabolism gene MURR1) domain, which functions as an interface for protein-protein interactions. Like MURR1, several of these factors also associate with and inhibit NF-kB. The proteins designated as COMMD or COMM domain containing 1-10 are extensively conserved in multicellular eukaryotic organisms and define a novel family of structural and functional homologs of MURR1. The prototype of this family, MURR1/COMMD1, suppresses NF-kB not by affecting nuclear translocation or binding of NF-kB to cognate motifs; rather, it functions in the nucleus by affecting the association of NF-kB with chromatin.
引用
收藏
页码:22222 / 22232
页数:11
相关论文
共 40 条
[1]   ABSOLUTE DEPENDENCE ON KAPPA-B RESPONSIVE ELEMENTS FOR INITIATION AND TAT-MEDIATED AMPLIFICATION OF HIV TRANSCRIPTION IN BLOOD CD4 T-LYMPHOCYTES [J].
ALCAMI, J ;
DELERA, TL ;
FOLGUEIRA, L ;
PEDRAZA, MA ;
JACQUE, JM ;
BACHELERIE, F ;
NORIEGA, AR ;
HAY, RT ;
HARRICH, D ;
GAYNOR, RB ;
VIRELIZIER, JL ;
ARENZANASEISDEDOS, F .
EMBO JOURNAL, 1995, 14 (07) :1552-1560
[2]   The NF-kappa B and I kappa B proteins: New discoveries and insights [J].
Baldwin, AS .
ANNUAL REVIEW OF IMMUNOLOGY, 1996, 14 :649-683
[3]   Control of oncogenesis and cancer therapy resistance by the transcription factor NF-κB [J].
Baldwin, AS .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 107 (03) :241-246
[4]   THE SAME INDUCIBLE NUCLEAR PROTEINS REGULATES MITOGEN ACTIVATION OF BOTH THE INTERLEUKIN-2 RECEPTOR-ALPHA GENE AND TYPE-1 HIV [J].
BOHNLEIN, E ;
LOWENTHAL, JW ;
SIEKEVITZ, M ;
BALLARD, DW ;
FRANZA, BR ;
GREENE, WC .
CELL, 1988, 53 (05) :827-836
[5]   Activation of IKKα target genes depends on recognition of specific κB binding sites by RelB:p52 dimers [J].
Bonizzi, G ;
Bebien, M ;
Otero, DC ;
Johnson-Vroom, KE ;
Cao, YX ;
Vu, D ;
Jegga, AG ;
Aronow, BJ ;
Ghosh, G ;
Rickert, RC ;
Karin, M .
EMBO JOURNAL, 2004, 23 (21) :4202-4210
[6]   A novel role for XIAP in copper homeostasis through regulation of MURR1 [J].
Burstein, E ;
Ganesh, L ;
Dick, RD ;
van de Sluis, B ;
Wilkinson, JC ;
Klomp, LWJ ;
Wijmenga, C ;
Brewer, GJ ;
Nabel, GJ ;
Duckett, CS .
EMBO JOURNAL, 2004, 23 (01) :244-254
[7]   Crystal structure of p50/p65 heterodimer of transcription factor NF-κB bound to DNA [J].
Chen, FE ;
Huang, DB ;
Chen, YQ ;
Ghosh, G .
NATURE, 1998, 391 (6665) :410-413
[8]   SIGNAL-INDUCED SITE-SPECIFIC PHOSPHORYLATION TARGETS I-KAPPA-B-ALPHA TO THE UBIQUITIN-PROTEASOME PATHWAY [J].
CHEN, ZJ ;
HAGLER, J ;
PALOMBELLA, VJ ;
MELANDRI, F ;
SCHERER, D ;
BALLARD, D ;
MANIATIS, T .
GENES & DEVELOPMENT, 1995, 9 (13) :1586-1597
[9]   Induction of nuclear factor kappa B by the CD30 receptor is mediated by TRAF1 and TRAF2 [J].
Duckett, CS ;
Gedrich, RW ;
Gilfillan, MC ;
Thompson, CB .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (03) :1535-1542
[10]   DIMERIZATION OF NF-KB2 WITH RELA(P65) REGULATES DNA-BINDING, TRANSCRIPTIONAL ACTIVATION, AND INHIBITION BY AN IKB-ALPHA (MAD-3) [J].
DUCKETT, CS ;
PERKINS, ND ;
KOWALIK, TF ;
SCHMID, RM ;
HUANG, ES ;
BALDWIN, AS ;
NABEL, GJ .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (03) :1315-1322