Coupled local translation and degradation regulate growth cone collapse. Academic Article uri icon

Overview

abstract

  • Local translation mediates axonal responses to Semaphorin3A (Sema3A) and other guidance cues. However, only a subset of the axonal proteome is locally synthesized, whereas most proteins are trafficked from the soma. The reason why only specific proteins are locally synthesized is unknown. Here we show that local protein synthesis and degradation are linked events in growth cones. We find that growth cones exhibit high levels of ubiquitination and that local signalling pathways trigger the ubiquitination and degradation of RhoA, a mediator of Sema3A-induced growth cone collapse. Inhibition of RhoA degradation is sufficient to remove the protein-synthesis requirement for Sema3A-induced growth cone collapse. In addition to RhoA, we find that locally translated proteins are the main targets of the ubiquitin-proteasome system in growth cones. Thus, local protein degradation is a major feature of growth cones and creates a requirement for local translation to replenish proteins needed to maintain growth cone responses.

publication date

  • April 22, 2015

Research

keywords

  • Growth Cones
  • Neurons
  • RNA, Messenger
  • Ubiquitin-Protein Ligases
  • rhoA GTP-Binding Protein

Identity

PubMed Central ID

  • PMC4408908

Scopus Document Identifier

  • 84928800989

Digital Object Identifier (DOI)

  • 10.1038/ncomms7888

PubMed ID

  • 25901863

Additional Document Info

volume

  • 6