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PMID: 10903184 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

The canonical Wg and JNK signaling cascades collaborate to promote both dorsal closure and ventral patterning.

Development (Cambridge, England) ·Vol. 127 ·No. 16 ·2000-08-00 ·Pages 3607-17

McEwen DG, Cox RT, Peifer M

Abstract

Elaboration of the Drosophila body plan depends on a series of cell-identity decisions and morphogenetic movements regulated by intercellular signals. For example, Jun N-terminal kinase signaling regulates cell fate decisions and morphogenesis during dorsal closure, while Wingless signaling regulates segmental patterning of the larval cuticle via Armadillo. wingless or armadillo mutant embryos secrete a lawn of ventral denticles; armadillo mutants also exhibit dorsal closure defects. We found that mutations in puckered, a phosphatase that antagonizes Jun N-terminal kinase, suppress in a dose-sensitive manner both the dorsal and ventral armadillo cuticle defects. Furthermore, we found that activation of the Jun N-terminal kinase signaling pathway suppresses armadillo-associated defects. Jun N-terminal kinase signaling promotes dorsal closure, in part, by regulating decapentaplegic expression in the dorsal epidermis. We demonstrate that Wingless signaling is also required to activate decapentaplegic expression and to coordinate cell shape changes during dorsal closure. Together, these results demonstrate that MAP-Kinase and Wingless signaling cooperate in both the dorsal and ventral epidermis, and suggest that Wingless may activate both the Wingless and the Jun N-terminal kinase signaling cascades.

MeSH Terms
Animals Armadillo Domain Proteins Body Patterning/physiology Drosophila/embryology,genetics,physiology Drosophila Proteins Enzyme Activation Insect Proteins/genetics,metabolism,physiology Mitogen-Activated Protein Kinase Kinases/genetics,metabolism Mutagenesis Phosphoprotein Phosphatases/genetics,physiology Proto-Oncogene Proteins/genetics,metabolism Signal Transduction/physiology Trans-Activators Transcription Factors Wnt1 Protein
Chemicals
ARM protein, Drosophila Armadillo Domain Proteins Drosophila Proteins Insect Proteins Proto-Oncogene Proteins Trans-Activators Transcription Factors Wnt1 Protein dpp protein, Drosophila wg protein, Drosophila Hep protein, Drosophila Mitogen-Activated Protein Kinase Kinases puc protein, Drosophila Phosphoprotein Phosphatases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
McEwen D G
Lineberger Comprehensive Cancer Center, Curriculum in Genetics and Molecular Biology, Department of Biology, The University of North Carolina, Chapel Hill, NC 27599-3280, USA.
Cox R T
Peifer M
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
2000-08-00
Pages
3607-17
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · 1F32GM19824 · United States
NCI NIH HHS · 5T32CA09156 · United States
NIGMS NIH HHS · R01GM47857 · United States
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