Tumour suppressor CYLD is a negative regulator of the mitotic kinase Aurora-B

• Published in: The Journal of pathology 2010-08, Vol.221 (4), p.425-432
• Main Authors: Sun, Lei, Gao, Jinmin, Huo, Lihong, Sun, Xiaoou, Shi, Xingjuan, Liu, Min, Li, Dengwen, Zhang, Chuanmao, Zhou, Jun
• Format: Article
• Language: English
• Subjects: Aurora Kinase B; Aurora Kinases; Aurora-B; Biological and medical sciences; Cell survival; Cells, Cultured; CYLD; deubiquitinase; Deubiquitinating Enzyme CYLD; Gene Knockdown Techniques; HeLa Cells; Humans; Investigative techniques, diagnostic techniques (general aspects); kinase activity; Medical sciences; Microscopy, Fluorescence; Mutation; Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques; Phosphoprotein phosphatase; Phosphorylation; PP2A; Protein Phosphatase 2 - metabolism; Protein-Serine-Threonine Kinases - metabolism; Tumor Suppressor Proteins - genetics; Tumor Suppressor Proteins - metabolism; Tumor Suppressor Proteins - physiology
• ISSN: 0022-3417; 1096-9896
• DOI: 10.1002/path.2723

The familial cylindromatosis tumour suppressor CYLD contains three cytoskeleton-associated protein glycine-rich (CAP-Gly) domains and a deubiquitinase domain. The tumour-suppressing function of CYLD has been attributed to its deubiquitinase domain, which removes lysine-63-linked polyubiquitin chains from target proteins, leading to the inhibition of cell survival and proliferation. In this study, we have detected an interaction of CYLD with the mitotic kinase Aurora-B. The interaction is mediated by the third CAP-Gly domain of CYLD and results in suppression of Aurora-B activity. Mechanistic studies reveal that the inhibition of Aurora-B activity by CYLD is independent of its deubiquitinase activity. Instead, CYLD interacts with protein phosphatase 2A (PP2A) and promotes the ability of PP2A to bind and dephosphorylate Aurora-B at threonine-232. Cylindromatosis-associated truncating mutations of CYLD abolish its interaction with PP2A, its enhancing effect on the PP2A/Aurora-B interaction, and its inhibitory effect on Aurora-B activity. These findings uncover Aurora-B and PP2A as novel binding partners of CYLD and suggest that CYLD negatively regulates Aurora-B activity through acting on the PP2A axis. Copyright © 2010 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.