Cic1, an adaptor protein specifically linking the 26S proteasome to its substrate, the SCF component Cdc4

被引:42
作者
Jäger, S [1 ]
Strayle, J [1 ]
Heinemeyer, W [1 ]
Wolf, DH [1 ]
机构
[1] Univ Stuttgart, Inst Biochem, D-70569 Stuttgart, Germany
关键词
Cdc4; Cic1; proteasome; protein degradation; SCF;
D O I
10.1093/emboj/20.16.4423
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
In eukaryotes, the ubiquitin-proteasome system plays a major role in selective protein breakdown for cellular regulation. Here we report the discovery of a new essential component of this degradation machinery. We found the Saccharomyces cerevisiae protein Cic1 attached to 26S proteasomes playing a crucial role in substrate specificity for proteasomal destruction. Whereas degradation of short-lived test proteins is not affected, cic1 mutants stabilize the F-box proteins Cdc4 and Grr1, substrate recognition subunits of the SCF complex. Cic1 interacts in vitro and in vivo with Cdc4, suggesting a function as a new kind of substrate recruiting factor or adaptor associated with the proteasome.
引用
收藏
页码:4423 / 4431
页数:9
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