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PMID: 10949042 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Drosophila segment borders result from unilateral repression of hedgehog activity by wingless signaling.

Molecular cell ·Vol. 6 ·No. 1 ·2000-07-00 ·Pages 203-9

Piepenburg O, Vorbrüggen G, Jäckle H

Abstract

Body structures of Drosophila develop through transient developmental units, termed parasegments, with boundaries lying between the adjacent expression domains of wingless and engrailed. Parasegments are transformed into the morphologically distinct segments that remain fixed. Segment borders are established adjacent and posterior to each engrailed domain. They are marked by single rows of stripe expressing cells that develop into epidermal muscle attachment sites. We show that the positioning of these cells is achieved through repression of Hedgehog signal transduction by Wingless signaling at the parasegment boundary. The nuclear mediators of the two signaling pathways, Cubitus interruptus and Pangolin, function as activator and symmetry-breaking repressor of stripe expression, respectively.

MeSH Terms
Animals Animals, Genetically Modified Base Sequence DNA/genetics DNA Primers/genetics Drosophila/genetics,growth & development,physiology Drosophila Proteins Gene Expression Regulation, Developmental Genes, Insect Genes, Reporter Hedgehog Proteins Insect Proteins/genetics,physiology Proto-Oncogene Proteins/genetics,physiology Signal Transduction Transcriptional Activation Wnt1 Protein
Chemicals
DNA Primers Drosophila Proteins Hedgehog Proteins Insect Proteins Proto-Oncogene Proteins Wnt1 Protein wg protein, Drosophila hh protein, Drosophila DNA
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Piepenburg O
Max-Planck-Institut für biophysikalische Chemie, Abteilung Molekulare Entwicklungsbiologie, Göttingen, Germany.
Vorbrüggen G
Jäckle H
Article Info
Journal
Molecular cell
Abbr.
Mol Cell
ISSN
1097-2765
Published
2000-07-00
Pages
203-9
Language
English
Region
United States
NLM ID
9802571
Subset
IM
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