Pentagone internalises glypicans to fine-tune multiple signalling pathways
Mark Norman,
Robin Vuilleumier,
Alexander Springhorn,
Jennifer Gawlik,
George Pyrowolakis
Affiliations
Mark Norman
Centre for Biological Signalling Studies, Albert-Ludwigs-University of Freiburg, Breisgau, Germany
Robin Vuilleumier
Institute for Biology I, Albert-Ludwigs-University of Freiburg, Breisgau, Germany
Alexander Springhorn
Institute for Biology I, Albert-Ludwigs-University of Freiburg, Breisgau, Germany; Spemann Graduate School of Biology and Medicine, Albert-Ludwigs-University of Freiburg, Breisgau, Germany
Jennifer Gawlik
Centre for Biological Signalling Studies, Albert-Ludwigs-University of Freiburg, Breisgau, Germany; Spemann Graduate School of Biology and Medicine, Albert-Ludwigs-University of Freiburg, Breisgau, Germany
Centre for Biological Signalling Studies, Albert-Ludwigs-University of Freiburg, Breisgau, Germany; Institute for Biology I, Albert-Ludwigs-University of Freiburg, Breisgau, Germany
Tight regulation of signalling activity is crucial for proper tissue patterning and growth. Here we investigate the function of Pentagone (Pent), a secreted protein that acts in a regulatory feedback during establishment and maintenance of BMP/Dpp morphogen signalling during Drosophila wing development. We show that Pent internalises the Dpp co-receptors, the glypicans Dally and Dally-like protein (Dlp), and propose that this internalisation is important in the establishment of a long range Dpp gradient. Pent-induced endocytosis and degradation of glypicans requires dynamin- and Rab5, but not clathrin or active BMP signalling. Thus, Pent modifies the ability of cells to trap and transduce BMP by fine-tuning the levels of the BMP reception system at the plasma membrane. In addition, and in accordance with the role of glypicans in multiple signalling pathways, we establish a requirement of Pent for Wg signalling. Our data propose a novel mechanism by which morphogen signalling is regulated.