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The dishevelled protein is modified by wingless signaling in Drosophila.

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Yanagawa, S, van Leeuwen, F, Wodarz, A, Klingensmith, J, Nusse, R·1995·Genes & Development

Abstract

Wingless (Wg) is an important signaling molecule in the development of Drosophila, but little is known about its signal transduction pathway. Genetic evidence indicates that another segment polarity gene, dishevelled (dsh) is required for Wg signaling. We have recently developed a cell culture system for Wg protein activity, and using this in vitro system as well as intact Drosophila embryos, we have analyzed biochemical changes in the Dsh protein as a consequence of Wg signaling. We find that Dsh is a phosphoprotein, normally present in the cytoplasm. Wg signaling generates a hyperphosphorylated form of Dsh, which is associated with a membrane fraction. Overexpressed Dsh becomes hyperphosphorylated in the absence of extracellular Wg and increases levels of the Armadillo protein, thereby mimicking the Wg signal. A deletional analysis of Dsh identifies several conserved domains essential for activity, among which is a so-called GLGF/DHR motif. We conclude that dsh, a highly conserved gene, is not merely a permissive factor in Wg signaling but encodes a novel signal transduction molecule, which may function between the Wg receptor and more downstream signaling molecules.

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Authors
Yanagawa, S., van Leeuwen, F., Wodarz, A., Klingensmith, J., & Nusse, R.
Venue
Genes & Development
Published
1995-05-01
Volume
9
Issue
9
Pages
1087-1097
ISSN
  • 0890-9369 (ISSN-L)
  • 1549-5477
OpenAlex
W2102512027
Cited by
388
References
0
Type
posted content
Language
en
Open access
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