Association of the mammalian proto-oncoprotein Int-6 with the three protein complexes eIF3, COP9 signalosome and 26S proteasome

被引:56
作者
Alves, KH [1 ]
Bochard, V [1 ]
Réty, S [1 ]
Jalinot, P [1 ]
机构
[1] Ecole Normale Super Lyon, Lab Biol Mol & Cellulaire, UMR5665, CNRS, F-69364 Lyon 07, France
关键词
Int-6; COP9; signalosome; 26S proteasome; eIF3; two-hybrid;
D O I
10.1016/S0014-5793(02)03147-2
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
The mammalian Int-6 protein has been characterized as a subunit of the eIF3 translation initiation factor and also as a transforming protein when its C-terminal part is deleted. It includes a protein domain, which also exists in various subunits of eIF3, of the 26S proteasome and of the CON signalosome (CSN). By performing a two-hybrid screen with Int-6 as bait, we have isolated subunits belonging to all three complexes, namely eIF3-p110, Rpt4, CSN3 and CSN6. The results of transient expression experiments in COS7 cells confirmed the interaction of Int-6 with Rpt4, CSN3 and CSN6, but also showed that Int-6 is able to bind another subunit of the CSN: CSN7a. Immunoprecipitation experiments performed with the endogenous proteins showed that Int-6 binds the entire CSN, but in low amount, and also that Int-6 is associated with the 26S proteasome. Taken together these results show that the Int-6 protein can bind the three complexes with various efficiencies, possibly exerting a regulatory activity in both protein translation and degradation. (C) 2002 Federation of European Biochemical Societies.
引用
收藏
页码:15 / 21
页数:7
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