Title | Coupled local translation and degradation regulate growth cone collapse. |
Publication Type | Journal Article |
Year of Publication | 2015 |
Authors | Deglincerti A, Liu Y, Colak D, Hengst U, Xu G, Jaffrey SR |
Journal | Nat Commun |
Volume | 6 |
Pagination | 6888 |
Date Published | 2015 Apr 22 |
ISSN | 2041-1723 |
Keywords | Animals, Axons, Blotting, Western, Electroporation, Embryo, Mammalian, Ganglia, Spinal, Growth Cones, HEK293 Cells, Hippocampus, Humans, Mice, Nerve Growth Factor, Neurons, PC12 Cells, Proteasome Endopeptidase Complex, Protein Biosynthesis, Rats, Rats, Sprague-Dawley, rhoA GTP-Binding Protein, RNA, Messenger, Semaphorin-3A, Spinal Cord, Ubiquitin-Protein Ligases, Ubiquitination |
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. |
DOI | 10.1038/ncomms7888 |
Alternate Journal | Nat Commun |
PubMed ID | 25901863 |
PubMed Central ID | PMC4408908 |
Grant List | R01 MH096702 / MH / NIMH NIH HHS / United States R01 NS056306 / NS / NINDS NIH HHS / United States K99/R00MH081058 / MH / NIMH NIH HHS / United States R21 MH086128 / MH / NIMH NIH HHS / United States R00 MH081058 / MH / NIMH NIH HHS / United States NS056306 / NS / NINDS NIH HHS / United States K99 MH081058 / MH / NIMH NIH HHS / United States MH086128 / MH / NIMH NIH HHS / United States |