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PMID: 9187151 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Negative regulation of Armadillo, a Wingless effector in Drosophila.

Development (Cambridge, England) ·Vol. 124 ·No. 11 ·1997-06-00 ·Pages 2255-66

Pai LM, Orsulic S, Bejsovec A, Peifer M

Abstract

Drosophila Armadillo and its vertebrate homolog beta-catenin play essential roles both in the transduction of Wingless/Wnt cell-cell signals and in the function of cell-cell adherens junctions. Wingless and Wnts direct numerous cell fate choices during development. We generated a mutant protein, Armadillo(S10), with a 54 amino acid deletion in its N-terminal domain. This mutant is constitutively active in Wingless signaling; its activity is independent of both Wingless signal and endogenous wild-type Armadillo. Armadillo's role in signal transduction is normally negatively regulated by Zeste-white 3 kinase, which modulates Armadillo protein stability. Armadillo(S10) is more stable than wild-type Armadillo, suggesting that it is less rapidly targeted for degradation. We show that Armadillo(S10) has escaped from negative regulation by Zeste white-3 kinase, and thus accumulates outside junctions even in the absence of Wingless signal. Finally, we present data implicating kinases in addition to Zeste white-3 in Armadillo phosphorylation. We discuss two models for the negative regulation of Armadillo in normal development and discuss how escape from this regulation contributes to tumorigenesis.

MeSH Terms
Amino Acid Sequence Animals Armadillo Domain Proteins Cell Adhesion Cell Membrane/chemistry Cell Nucleus/chemistry Cytoplasm/chemistry Drosophila/embryology Drosophila Proteins Gene Expression Regulation, Developmental/physiology Glycogen Synthase Kinase 3 Homeodomain Proteins/analysis Insect Proteins/analysis,genetics,metabolism Intercellular Junctions/chemistry Molecular Sequence Data Phosphorylation Protein Serine-Threonine Kinases/genetics,physiology Proto-Oncogene Proteins/analysis,physiology Recombinant Fusion Proteins Sequence Deletion Signal Transduction/physiology Trans-Activators Transcription Factors Wnt1 Protein
Chemicals
ARM protein, Drosophila Armadillo Domain Proteins Drosophila Proteins Homeodomain Proteins Insect Proteins Proto-Oncogene Proteins Recombinant Fusion Proteins Trans-Activators Transcription Factors Wnt1 Protein engrailed homeobox proteins wg protein, Drosophila Protein Serine-Threonine Kinases Sgg protein, Drosophila Glycogen Synthase Kinase 3
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Pai L M
Department of Biology and Curriculum in Genetics and Molecular Biology, University of North Carolina, Chapel Hill 27599-3280, USA.
Orsulic S
Bejsovec A
Peifer M
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1997-06-00
Pages
2255-66
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · GM47857 · United States
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