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The E3 Ubiquitin Ligase MID1 Catalyzes Ubiquitination and Cleavage of Fu

Authors :
Sybille Krauß
Eva-Christina Müller
Frank Matthes
Melanie Fuchs
Andrea Köhler
Stephanie Dorn
Rainer Schneider
Susann Schweiger
Erich E. Wanker
Source :
The journal of biological chemistry 289(46), 31805-31817 (2014). doi:10.1074/jbc.M113.541219
Publication Year :
2014
Publisher :
Elsevier BV, 2014.

Abstract

Sonic Hedgehog (SHH)-GLI signalling plays an important role during embryogenesis and in tumorigenesis. The survival and growth of several types of cancer depend on autonomously activated SHH-GLI signalling. A protein complex containing the ubiquitin-ligase MID1 and protein phosphatase 2A (PP2A) regulates the nuclear localization and transcriptional activity of GLI3, a transcriptional effector molecule of SHH, in cancer cell lines with autonomously activated SHH signalling. However, the exact molecular mechanisms that mediate the interaction between MID1 and GLI3 remained unknown. Here, we show that MID1 catalyses the ubiquitination and proteasomal cleavage of the GLI3-regulator Fu. Our data suggest that Fu ubiquitination and cleavage is one of the key elements connecting the MID1/PP2A protein complex with GLI3 activity control.

Details

ISSN :
00219258
Volume :
289
Database :
OpenAIRE
Journal :
Journal of Biological Chemistry
Accession number :
edsair.doi.dedup.....9689225db772ca0bd39e977d475f56d2
Full Text :
https://doi.org/10.1074/jbc.m113.541219