The GTPase Rab8 differentially controls the long- and short-range activity of the Hedgehog morphogen gradient by regulating Hedgehog apico-basal distribution

Development. 2021 Mar 9;148(5):dev191791. doi: 10.1242/dev.191791.

Abstract

The Hedgehog (Hh) morphogen gradient is required for patterning during metazoan development, yet the mechanisms involved in Hh apical and basolateral release and how this influences short- and long-range target induction are poorly understood. We found that depletion of the GTPase Rab8 in Hh-producing cells induces an imbalance between the level of apically and laterally released Hh. This leads to non-cell-autonomous differential effects on the expression of Hh target genes, namely an increase in its short-range targets and a concomitant decrease in long-range targets. We further found that Rab8 regulates the endocytosis and apico-basal distribution of Ihog, a transmembrane protein known to bind to Hh and to be crucial for establishment of the Hh gradient. Our data provide new insights into morphogen gradient formation, whereby morphogen activity is functionally distributed between apically and basolaterally secreted pools.

Keywords: Hedgehog; Interference-of-Hedgehog; Morphogen gradient; Polarized secretion; Rab8; Trafficking.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Genetically Modified / metabolism
  • Drosophila / metabolism*
  • Drosophila Proteins / antagonists & inhibitors
  • Drosophila Proteins / genetics
  • Drosophila Proteins / metabolism*
  • Endocytosis
  • Endosomes / metabolism
  • GTP Phosphohydrolases / antagonists & inhibitors
  • GTP Phosphohydrolases / genetics
  • GTP Phosphohydrolases / metabolism*
  • Gene Expression Regulation
  • Hedgehog Proteins / genetics
  • Hedgehog Proteins / metabolism*
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Mutagenesis
  • Protein Stability
  • RNA Interference
  • RNA, Double-Stranded / metabolism
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / metabolism
  • Signal Transduction

Substances

  • Drosophila Proteins
  • Hedgehog Proteins
  • Membrane Glycoproteins
  • RNA, Double-Stranded
  • Receptors, Cell Surface
  • dpp protein, Drosophila
  • iHog protein, Drosophila
  • hh protein, Drosophila
  • GTP Phosphohydrolases
  • Rab8 protein, Drosophila