4.8 Article

NEDD8 recruits E2-ubiquitin to SCF E3 ligase

Journal

EMBO JOURNAL
Volume 20, Issue 15, Pages 4003-4012

Publisher

WILEY
DOI: 10.1093/emboj/20.15.4003

Keywords

I kappa B alpha; NEDD8; ROC1-SCF; ubiquitylation; ubiquitin ligase

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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.

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