Regulation of axon guidance by compartmentalized nonsense-mediated mRNA decay. Academic Article uri icon

Overview

abstract

  • Growth cones enable axons to navigate toward their targets by responding to extracellular signaling molecules. Growth-cone responses are mediated in part by the local translation of axonal messenger RNAs (mRNAs). However, the mechanisms that regulate local translation are poorly understood. Here we show that Robo3.2, a receptor for the Slit family of guidance cues, is synthesized locally within axons of commissural neurons. Robo3.2 translation is induced by floor-plate-derived signals as axons cross the spinal cord midline. Robo3.2 is also a predicted target of the nonsense-mediated mRNA decay (NMD) pathway. We find that NMD regulates Robo3.2 synthesis by inducing the degradation of Robo3.2 transcripts in axons that encounter the floor plate. Commissural neurons deficient in NMD proteins exhibit aberrant axonal trajectories after crossing the midline, consistent with misregulation of Robo3.2 expression. These data show that local translation is regulated by mRNA stability and that NMD acts locally to influence axonal pathfinding.

publication date

  • June 6, 2013

Research

keywords

  • Axons
  • Embryo, Mammalian
  • Growth Cones
  • Membrane Proteins
  • Nerve Tissue Proteins
  • Nonsense Mediated mRNA Decay
  • Spinal Cord

Identity

PubMed Central ID

  • PMC3685487

Scopus Document Identifier

  • 84878888946

Digital Object Identifier (DOI)

  • 10.1016/j.cell.2013.04.056

PubMed ID

  • 23746841

Additional Document Info

volume

  • 153

issue

  • 6