NEDD8 recruits E2-ubiquitin to SCF E3 ligase

被引:251
作者
Kawakami, T
Chiba, T
Suzuki, T
Iwai, K
Yamanaka, K
Minato, N
Suzuki, H
Shimbara, N
Hidaka, Y
Osaka, F
Omata, M
Tanaka, K
机构
[1] Tokyo Metropolitan Inst Med Sci, Bunkyo Ku, Tokyo 1138613, Japan
[2] Japan Sci & Technol Corp, JST, CREST, Tokyo 1138613, Japan
[3] Univ Tokyo, Fac Med, Dept Gastroenterol, Bunkyo Ku, Tokyo 1138655, Japan
[4] Kyoto Univ, Grad Sch Biostudies, Dept Mol & Syst Biol, Kyoto 6068501, Japan
[5] Yamanouchi Pharmaceut Co Ltd, Inst Drug Discovery Res, Tsukuba, Ibaraki 3058585, Japan
[6] Sumitomo Elect Ind Ltd, Sakae Ku, Yokohama, Kanagawa 2448588, Japan
[7] Sagami Chem Res Ctr, Japan Sci & Technol Corp, ERATO, Kato Cytoprot Network Project, Sagamihara, Kanagawa 2290012, Japan
关键词
I kappa B alpha; NEDD8; ROC1-SCF; ubiquitylation; ubiquitin ligase;
D O I
10.1093/emboj/20.15.4003
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
NEDD8/Rub1 is a ubiquitin (Ub)-like post-translational modifier that is covalently linked to cullin (Cul)-family proteins in a manner analogous to ubiquitylation. NEDD8 is known to enhance the ubiquitylating activity of the SCF complex (composed of Skp1, Cul-1, ROC1 and F-box protein), but the mechanistic role is largely unknown. Using an in vitro reconstituted system, we report here that NEDD8 modification of Cull enhances recruitment of Ub-conjugating enzyme Ubc4 (E2) to the SCF complex (E3). This recruitment requires thioester linkage of Ub to Ubc4. Our findings indicate that the NEDD8-modifying system accelerates the formation of the E2-E3 complex, which stimulates protein polyubiquitylation.
引用
收藏
页码:4003 / 4012
页数:10
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