Patched1-ArhGAP36-PKA-Inversin axis determines the ciliary translocation of Smoothened for Sonic Hedgehog pathway activation

Proc Natl Acad Sci U S A. 2019 Jan 15;116(3):874-879. doi: 10.1073/pnas.1804042116. Epub 2018 Dec 31.

Abstract

The Sonic Hedgehog (Shh) pathway conducts primarily in the primary cilium and plays important roles in cell proliferation, individual development, and tumorigenesis. Shh ligand binding with its ciliary membrane-localized transmembrane receptor Patched1 results in the removal of Patched1 from and the translocation of the transmembrane oncoprotein Smoothened into the cilium, leading to Shh signaling activation. However, how these processes are coupled remains unknown. Here, we show that the Patched1-ArhGAP36-PKA-Inversin axis determines the ciliary translocation of Smoothened. We find that Patched1 interacts with and stabilizes the PKA negative regulator ArhGAP36 to the centrosome. Activating the Shh pathway results in the removal of ArhGAP36 from the mother centriole and the centrosomal PKA accumulation. This PKA then phosphorylates Inversin and promotes its interaction with and the ciliary translocation of Smoothened. Knockdown of Inversin disrupts the ciliary translocation of Smoothened and Shh pathway activation. These findings reveal a regulatory molecular mechanism for the initial step of Shh pathway activation.

Keywords: Inversin; PKA; Patched1; Smoothened; Sonic Hedgehog pathway.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cilia / metabolism*
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • GTPase-Activating Proteins / metabolism
  • HEK293 Cells
  • Hedgehog Proteins / metabolism*
  • Humans
  • Mice
  • Patched-1 Receptor / metabolism*
  • Phosphorylation
  • Signal Transduction
  • Smoothened Receptor / metabolism*
  • Transcription Factors / metabolism*

Substances

  • ARHGAP36 protein, human
  • GTPase-Activating Proteins
  • Hedgehog Proteins
  • INVS protein, human
  • Patched-1 Receptor
  • Smoothened Receptor
  • Transcription Factors
  • Cyclic AMP-Dependent Protein Kinases