Dpp signaling promotes the cuboidal-to-columnar shape transition of Drosophila wing disc epithelia by regulating Rho1

Research output: Contribution to journalResearch articleContributedpeer-review

Contributors

  • Thomas J. Widmann - , Max Planck Institute of Molecular Cell Biology and Genetics (First author)
  • Christian Dahmann - , Chair of Systems Biology and Genetics, Max Planck Institute of Molecular Cell Biology and Genetics (Author)

Abstract

Morphogenesis is largely driven by changes in the shape of individual cells. However, how cell shape is regulated in developing animals is not well understood. Here, we show that the onset of TGFbeta/Dpp signaling activity correlates with the transition from cuboidal to columnar cell shape in developing Drosophila melanogaster wing disc epithelia. Dpp signaling is necessary for maintaining this elongated columnar cell shape and overactivation of the Dpp signaling pathway results in precocious cell elongation. Moreover, we provide evidence that Dpp signaling controls the subcellular distribution of the activities of the small GTPase Rho1 and the regulatory light chain of non-muscle myosin II (MRLC). Alteration of Rho1 or MRLC activity has a profound effect on apical-basal cell length. Finally, we demonstrate that a decrease in Rho1 or MRLC activity rescues the shortening of cells with compromised Dpp signaling. Our results identify a cell-autonomous role for Dpp signaling in promoting and maintaining the elongated columnar shape of wing disc cells and suggest that Dpp signaling acts by regulating Rho1 and MRLC.

Details

Original languageEnglish
Pages (from-to)1362-1373
Number of pages12
JournalJournal of Cell Science
Volume122
Issue number9
Publication statusPublished - 1 May 2009
Peer-reviewedYes

External IDs

Scopus 67650541310

Keywords

DFG Classification of Subject Areas according to Review Boards

Subject groups, research areas, subject areas according to Destatis

Keywords

  • Drosophila, Wing imaginal disc, Cell shape, Cell extrusion, Dpp, Tkv, Brk, Rho1, RhoGEF2, Myosin II

Library keywords