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PMID: 1335365 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

wingless signaling acts through zeste-white 3, the Drosophila homolog of glycogen synthase kinase-3, to regulate engrailed and establish cell fate.

Cell ·Vol. 71 ·No. 7 ·1992-12-24 ·Pages 1167-79

Siegfried E, Chou TB, Perrimon N

Abstract

Intrasegmental patterning in the Drosophila embryo is regulated by cell-cell communication. One of the signaling pathways that operates to specify positional information throughout the segment is mediated by the wingless (wg) protein, which is the homolog of the proto-oncogene Wnt-1. The early role of wg is to stabilize engrailed (en) expression by initiating a phase of en autoregulation in the adjacent more posterior cells. Here, we report that the segment polarity gene zeste-white 3 (zw3; also known as shaggy) acts as a repressor of en autoregulation. Genetic epistasis experiments indicate that wg signaling operates by inactivating the zw3 repression of en autoactivation. In addition, we demonstrate that zw3 encodes the Drosophila homolog of mammalian glycogen synthase kinase-3.

Related Genes
MeSH Terms
Amino Acid Sequence Animals Calcium-Calmodulin-Dependent Protein Kinases Cell Communication Drosophila/embryology,genetics Gene Expression Regulation Glycogen Synthase Kinases Molecular Sequence Data Protein Kinases/genetics Sequence Homology, Amino Acid Signal Transduction
Chemicals
Protein Kinases Glycogen Synthase Kinases Calcium-Calmodulin-Dependent Protein Kinases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Siegfried E
Department of Genetics, Harvard Medical School, Boston, Massachusetts 02115.
Chou T B
Perrimon N
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1992-12-24
Pages
1167-79
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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