The Cyclophilin-like Domain of Ran-binding Protein-2 Modulates Selectively the Activity of the Ubiquitin-Proteasome System and Protein Biogenesis

• Published in: The Journal of biological chemistry Vol. 282; no. 48; pp. 34770 - 34778
• Main Authors: Yi, Haiqing, Friedman, Julie L., A. Ferreira, Paulo
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 30-11-2007; American Society for Biochemistry and Molecular Biology
• Subjects: Amino Acid Motifs; Animals; Bacterial Proteins - chemistry; Cattle; Cell Line; Chlorocebus aethiops; COS Cells; Cyclophilins - chemistry; Enzyme Inhibitors - pharmacology; Luminescent Proteins - chemistry; Models, Genetic; Molecular Chaperones - chemistry; Molecular Chaperones - physiology; Nuclear Pore Complex Proteins - chemistry; Nuclear Pore Complex Proteins - physiology; Proteasome Endopeptidase Complex - chemistry; Proteasome Endopeptidase Complex - metabolism; Proteasome Inhibitors; Protein Structure, Tertiary; Proteins - chemistry; Recombinant Fusion Proteins - chemistry; Ubiquitin - chemistry
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M706903200

The ubiquitin-proteasome system (UPS) plays a critical role in protein degradation. The 19S regulatory particle (RP) of the 26S proteasome mediates the recognition, deubiquitylation, unfolding, and channeling of ubiquitylated substrates to the 20S proteasome. Several subunits of the 19S RP interact with a growing number of factors. The cyclophilin-like domain (CLD) of Ran-binding protein-2 (RanBP2/Nup358) associates specifically with at least one subunit, S1, of the base subcomplex of the 19S RP, but the functional implications of this interaction on the UPS activity are elusive. This study shows the CLD of RanBP2 promotes selectively the accumulation of a subset of reporter substrates of the UPS, such as the ubiquitin (Ub)-fusion yellow fluorescent protein (YFP) degradation substrate, UbG76V-YFP, and the N-end rule substrate, Ub-R-YFP. Conversely, the degradation of endoplasmic reticulum and misfolded proteins, and of those linked to UPS-independent degradation, is not affected by CLD. The selective effect of CLD on the UPS in vivo is independent of, and synergistic with, proteasome inhibitors, and CLD does not affect the intrinsic proteolytic activity of the 20S proteasome. The inhibitory activity of CLD on the UPS resides in a purported SUMO binding motif. We also found two RanBP2 substrates, RanGTPase-activating protein and retinitis pigmentosa GTPase regulator interacting protein-1α1, whose steady-state levels are selectively modulated by CLD. Hence, the CLD of RanBP2 acts as a novel auxiliary modulator of the UPS activity; it may contribute to the molecular and subcellular compartmentation of the turnover of properly folded proteins and modulation of the expressivity of several neurological diseases.