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The E3 Ubiquitin Ligase MID1 Catalyzes Ubiquitination and Cleavage of Fu
- 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.
- Subjects :
- metabolism [Microtubule Proteins]
Ubiquitin-conjugating enzyme
Biochemistry
metabolism [Protein Serine-Threonine Kinases]
Ubiquitin
metabolism [Transcription Factors]
Nuclear protein
Sonic hedgehog
biology
metabolism [Protein-Serine-Threonine Kinases]
Nuclear Proteins
respiratory system
Protein-Serine-Threonine Kinases
Ubiquitin ligase
Gene Expression Regulation, Neoplastic
GLI3 protein, human
ddc:540
embryonic structures
Microtubule Proteins
metabolism [Hedgehog Proteins]
Function and Dysfunction of the Nervous System
metabolism [Nuclear Proteins]
Signal Transduction
metabolism [Kruppel-Like Transcription Factors]
Proteasome Endopeptidase Complex
animal structures
STK36 protein, human
Ubiquitin-Protein Ligases
Kruppel-Like Transcription Factors
Nerve Tissue Proteins
Protein Serine-Threonine Kinases
chemistry [Ubiquitin-Protein Ligases]
Catalysis
Zinc Finger Protein Gli3
Cell Line, Tumor
GLI3
Humans
Hedgehog Proteins
metabolism [Proteasome Endopeptidase Complex]
metabolism [Cell Nucleus]
Molecular Biology
chemistry [Lysine]
DNA Primers
Cell Nucleus
metabolism [Nerve Tissue Proteins]
Lysine
Ubiquitination
Cell Biology
Protein phosphatase 2
chemistry [Ubiquitin]
Proteasome
biology.protein
SHH protein, human
human activities
Mid1 protein, human
HeLa Cells
Transcription Factors
Subjects
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