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Negative regulation of Armadillo, a Wingless effector in Drosophila

  • Li Mei Pai
  • , Sandra Orsulic
  • , Amy Bejsovec
  • , Mark Peifer*
  • *此作品的通信作者
  • University of North Carolina at Chapel Hill
  • Max Planck Institute of Immunobiology and Epigenetics
  • Northwestern University

研究成果: 期刊稿件文章同行評審

264 引文 斯高帕斯(Scopus)

摘要

Drosophila Armadillo and its vertebrate homolog β-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 rated 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.

原文英語
頁(從 - 到)2255-2266
頁數12
期刊Development (Cambridge)
124
發行號11
出版狀態已出版 - 06 1997
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