PUBLICATION

Functional Genomic Analysis of the Wnt-Wingless Signaling Pathway

Authors
Dasgupta, R., Kaykas, A., Moon, R.T., and Perrimon, N.
ID
ZDB-PUB-050413-18
Date
2005
Source
Science (New York, N.Y.)   308(5723): 826-833 (Journal)
Registered Authors
Moon, Randall T.
Keywords
none
MeSH Terms
  • Wnt3 Protein
  • Phosphorylation
  • Transcription Factors/chemistry
  • Transcription Factors/genetics
  • Transcription Factors/metabolism
  • Cloning, Molecular
  • Proto-Oncogene Proteins/genetics
  • Proto-Oncogene Proteins/metabolism*
  • Animals
  • Zebrafish
  • Protein Kinases/metabolism
  • beta Catenin
  • Genes, Reporter
  • Genes, Insect
  • Drosophila Proteins/chemistry
  • Drosophila Proteins/genetics
  • Drosophila Proteins/metabolism*
  • Genomics*
  • Wnt Proteins
  • Binding Sites
  • Computational Biology
  • Cell Line
  • Epistasis, Genetic
  • Signal Transduction*
  • Embryonic Development
  • Embryo, Nonmammalian/metabolism
  • Mutation
  • Drosophila melanogaster/genetics*
  • Drosophila melanogaster/metabolism
  • Transfection
  • Gene Expression Regulation*
  • Cytoskeletal Proteins/metabolism
  • Phenotype
  • RNA Interference*
  • Wnt1 Protein
  • Trans-Activators/metabolism
  • rab5 GTP-Binding Proteins/genetics
  • rab5 GTP-Binding Proteins/metabolism
  • Zebrafish Proteins
  • Proteins/metabolism
PubMed
15817814 Full text @ Science
Abstract
The Wnt-Wingless (Wg) pathway is one of a core set of evolutionarily conserved signaling pathways that regulates many aspects of metazoan development. Aberrant Wnt signaling has been linked to human disease. In the present study we used a genomewide RNA interference (RNAi) screen in Drosophila cells to screen for regulators of the Wnt pathway. We identified 238 potential regulators, which include known pathway components, genes with functions not previously linked to this pathway, and genes with no previously assigned functions. Reciprocal-Best-Blast analyses reveal that 50% of the genes identified in the screen have human orthologs of which ~18% are associated with human disease. Functional assays of selected genes from the cell-based screen in Drosophila, mammalian cells, and zebrafish embryos demonstrated that these genes have evolutionarily conserved functions in Wnt signaling. High throughput RNAi screens in cultured cells, followed by functional analyses in model organisms, proves to be a rapid means of identifying regulators of signaling pathways implicated in development and disease.
Genes / Markers
Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping