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Chibby, a nuclear beta-catenin-associated antagonist of the Wnt/Wingless pathway
- Source :
- Nature. 422(6934)
- Publication Year :
- 2002
-
Abstract
- Inappropriate activation of downstream target genes by the oncoprotein beta-catenin is implicated in development of numerous human cancers. beta-catenin and its fruitfly counterpart Armadillo act as a coactivator in the canonical Wnt/Wingless pathway by binding to Tcf/Lef transcription factors. Here we report a conserved nuclear protein, named Chibby, which was identified in a screen for proteins that directly interact with the C-terminal region of beta-catenin. In mammalian cultured cells we demonstrate that Chibby inhibits beta-catenin-mediated transcriptional activation by competing with Lef-1 to bind to beta-catenin. Inhibition of Drosophila Chibby by RNA interference results in segment polarity defects that mimick a wingless gain-of-function phenotype, and overexpression of the wingless target genes engrailed and Ultrabithorax. In addition, epistasis experiments indicate that chibby acts downstream of wingless and upstream of armadillo.
- Subjects :
- Transcriptional Activation
animal structures
Beta-catenin
Lymphoid Enhancer-Binding Factor 1
Molecular Sequence Data
Wnt1 Protein
Cell Line
Proto-Oncogene Proteins
Coactivator
Animals
Drosophila Proteins
Humans
RNA, Messenger
Nuclear protein
Transcription factor
Ultrabithorax
Conserved Sequence
beta Catenin
Genetics
Armadillo Domain Proteins
Homeodomain Proteins
Multidisciplinary
Binding Sites
integumentary system
biology
fungi
Wnt signaling pathway
Nuclear Proteins
Epistasis, Genetic
Zebrafish Proteins
engrailed
Cell biology
DNA-Binding Proteins
Wnt Proteins
Cytoskeletal Proteins
Drosophila melanogaster
Phenotype
Catenin
embryonic structures
COS Cells
biology.protein
Trans-Activators
RNA Interference
Carrier Proteins
Protein Binding
Signal Transduction
Transcription Factors
Subjects
Details
- ISSN :
- 00280836
- Volume :
- 422
- Issue :
- 6934
- Database :
- OpenAIRE
- Journal :
- Nature
- Accession number :
- edsair.doi.dedup.....4913c5eab2571dd261882917f1c2da48