The structure and regulation of Cullin 2 based E3 ubiquitin ligases and their biological functions. Issue 1 (March 2016)

• Record Type: Journal Article
• Authors: Cai, Weijia; Yang, Haifeng
• Is Part Of: Cell division. Volume 11:Issue 1(2016)
• Page Start: 1
• Page End: 11
• Publication Date: 2016-03
• Subjects: Cullin-2 -- Elongin -- E3 ubiquitin ligase -- VHL -- Hypoxia inducible factor -- Rack1 -- E4orf6 -- Viral host defense; Cell division -- Periodicals; 571.844
• DOI: 10.1186/s13008-016-0020-7
• Languages: English
• ISSNs: 1747-1028

Abstract

Abstract Background Cullin-RING E3 ubiquitin ligase complexes play a central role in targeting cellular proteins for ubiquitination-dependent protein turnover through 26S proteasome. Cullin-2 is a member of the Cullin family, and it serves as a scaffold protein for Elongin B and C, Rbx1 and various substrate recognition receptors to form E3 ubiquitin ligases. Main body of the abstract First, the composition, structure and the regulation of Cullin-2 based E3 ubiquitin ligases were introduced. Then the targets, the biological functions of complexes that use VHL, Lrr-1, Fem1b, Prame, Zyg-11, BAF250, Rack1 as substrate targeting subunits were described, and their involvement in diseases was discussed. A small molecule inhibitor of Cullins as a potential anti-cancer drug was introduced. Furthermore, proteins with VHL box that might bind to Cullin-2 were described. Finally, how different viral proteins form E3 ubiquitin ligase complexes with Cullin-2 to counter host viral defense were explained. Conclusions Cullin-2 based E3 ubiquitin ligases, using many different substrate recognition receptors, recognize a number of substrates and regulate their protein stability. These complexes play critical roles in biological processes and diseases such as cancer, germline differentiation and viral defense. Through the better understanding of their biology, we can devise and develop new therapeutic strategies to treat cancers, inherited diseases and viral infections.