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SCF (Fbxl17) ubiquitylation of Sufu regulates Hedgehog signaling and medulloblastoma development

Raducu, Madalina; Fung, Ella; Serres, Sebastien; Infante, Paola; Barberis, Alessandro; Fischer, Roman; Bristow, Claire; Th�z�nas, Marie?La�titia; Finta, Csaba; Christianson, John C.; Buffa, Francesca M.; Kessler, Benedikt M.; Sibson, Nicola R.; Di Marcotullio, Lucia; Toftg�rd, Rune; D'Angiolella, Vincenzo

SCF (Fbxl17) ubiquitylation of Sufu regulates Hedgehog signaling and medulloblastoma development Thumbnail


Authors

Madalina Raducu

Ella Fung

SEBASTIEN SERRES Sebastien.Serres@nottingham.ac.uk
Assistant Professor in Metabolic Biochemistry

Paola Infante

Alessandro Barberis

Roman Fischer

Claire Bristow

Marie?La�titia Th�z�nas

Csaba Finta

John C. Christianson

Francesca M. Buffa

Benedikt M. Kessler

Nicola R. Sibson

Lucia Di Marcotullio

Rune Toftg�rd

Vincenzo D'Angiolella



Abstract

Skp1‐Cul1‐F‐box protein (SCF) ubiquitin ligases direct cell survival decisions by controlling protein ubiquitylation and degradation. Sufu (Suppressor of fused) is a central regulator of Hh (Hedgehog) signaling and acts as a tumor suppressor by maintaining the Gli (Glioma‐associated oncogene homolog) transcription factors inactive. Although Sufu has a pivotal role in Hh signaling, the players involved in controlling Sufu levels and their role in tumor growth are unknown. Here, we show that Fbxl17 (F‐box and leucine‐rich repeat protein 17) targets Sufu for proteolysis in the nucleus. The ubiquitylation of Sufu, mediated by Fbxl17, allows the release of Gli1 from Sufu for proper Hh signal transduction. Depletion of Fbxl17 leads to defective Hh signaling associated with an impaired cancer cell proliferation and medulloblastoma tumor growth. Furthermore, we identify a mutation in Sufu, occurring in medulloblastoma of patients with Gorlin syndrome, which increases Sufu turnover through Fbxl17‐mediated polyubiquitylation and leads to a sustained Hh signaling activation. In summary, our findings reveal Fbxl17 as a novel regulator of Hh pathway and highlight the perturbation of the Fbxl17–Sufu axis in the pathogenesis of medulloblastoma.

Citation

Raducu, M., Fung, E., Serres, S., Infante, P., Barberis, A., Fischer, R., …D'Angiolella, V. (2016). SCF (Fbxl17) ubiquitylation of Sufu regulates Hedgehog signaling and medulloblastoma development. EMBO Journal, 35(13), 1400-1416. https://doi.org/10.15252/embj.201593374

Journal Article Type Article
Acceptance Date Apr 29, 2016
Online Publication Date May 27, 2016
Publication Date Jul 1, 2016
Deposit Date Mar 8, 2017
Publicly Available Date Nov 26, 2019
Print ISSN 0261-4189
Electronic ISSN 1460-2075
Publisher EMBO Press
Peer Reviewed Peer Reviewed
Volume 35
Issue 13
Pages 1400-1416
DOI https://doi.org/10.15252/embj.201593374
Public URL http://www.ncbi.nlm.nih.gov/pubmed/27234298
Publisher URL http://emboj.embopress.org/content/35/13/1400

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