NEDD8 Overexpression Results in Neddylation of Ubiquitin Substrates by the Ubiquitin Pathway

被引:55
作者
Hjerpe, Roland [1 ]
Thomas, Yann [1 ]
Kurz, Thimo [1 ]
机构
[1] Univ Dundee, Scottish Inst Cell Signalling, Prot Ubiquitylat Unit, Dundee DD1 5EH, Scotland
关键词
NEDD8; ubiquitin; p53; Caspase; 7; ubiquitin E1 enzyme;
D O I
10.1016/j.jmb.2012.05.013
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Ubiquitin and ubiquitin-like proteins use unique E1, E2, and E3 enzymes for conjugation to their substrates. We and others have recently reported that increases in the relative concentration of the ubiquitin-like protein NEDD8 over ubiquitin lead to activation of NEDD8 by the ubiquitin E1 enzyme. We now show that this results in erroneous conjugation of NEDD8 to ubiquitin substrates, such as p53, Caspase 7, and Hif1 alpha, demonstrating that overexpression of NEDD8 is not appropriate for identification of substrates of the NEDD8 pathway. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:27 / 29
页数:3
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