T2BP, a novel TRAF2 binding protein, can activate NF-κB and AP-1 without TNF stimulation

被引:55
作者
Kanamori, M
Suzuki, H
Saito, R
Muramatsu, M
Hayashizaki, Y
机构
[1] RIKEN, GSC, Lab Genome Explorat Res Grp, Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] RIKEN, Genome Sci Lab, Wako, Saitama 3510198, Japan
关键词
TNF; TRAF2; FHA; two-hybrid; protein-protein interactions; NF-kappa B; AP-1;
D O I
10.1006/bbrc.2001.6315
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
TRAF2 is a key molecule involved in TNF signaling, which is crucial for the regulation of inflammatory processes. We have identified a novel TRAF2 binding protein, designated as T2BP (TRAF2 binding protein), by a mammalian two-hybrid screening approach. T2BP is a relatively small protein of 184 amino acids, which includes a forkhead-associated domain, the phosphopeptide binding motif. The interaction domain search showed that the TRAF domain in TRAF2 is required for the binding to T2BP whereas almost the entire protein in T2BP binds to TRAF2. The interaction was further confirmed by co-immunoprecipitation. Expression profiling for T2BP and TRAF2 revealed an ubiquitous expression in adult mouse tissues. Overexpression of T2BP in HEK293 cells activated NF-kappaB and AP-1 in a dose dependent manner as well as seen in the TNF-treated control cells. Our results suggest that T2BP is involved in the TNF-mediated signaling by its interaction with TRAF2. (C) 2002 Elsevier Science (USA).
引用
收藏
页码:1108 / 1113
页数:6
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