Cargando…

Commissureless Regulation of Axon Outgrowth across the Midline Is Independent of Rab Function

Nervous system function requires that neurons within neural circuits are connected together precisely. These connections form during the process of axon guidance whereby each neuron extends an axon that migrates, often large distances, through a complex environment to reach its synaptic target. This...

Descripción completa

Detalles Bibliográficos
Autores principales: van den Brink, Daan M., Banerji, Oishik, Tear, Guy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655966/
https://www.ncbi.nlm.nih.gov/pubmed/23696892
http://dx.doi.org/10.1371/journal.pone.0064427
_version_ 1782269958897532928
author van den Brink, Daan M.
Banerji, Oishik
Tear, Guy
author_facet van den Brink, Daan M.
Banerji, Oishik
Tear, Guy
author_sort van den Brink, Daan M.
collection PubMed
description Nervous system function requires that neurons within neural circuits are connected together precisely. These connections form during the process of axon guidance whereby each neuron extends an axon that migrates, often large distances, through a complex environment to reach its synaptic target. This task can be simplified by utilising intermediate targets to divide the route into smaller sections. This requires that axons adapt their behaviour as they migrate towards and away from intermediate targets. In the central nervous system the midline acts as an intermediate target for commissural axons. In Drosophila commissural axons switch from attraction towards to extension away from the midline by regulating the levels of the Roundabout receptor on their cell surface. This is achieved by Commissureless which directs Roundabout to an intracellular compartment in the soma prior to reaching the midline. Once across the midline Roundabout is allowed to reach the surface and acts as a receptor for the repellent ligand Slit that is secreted by cells at the midline. Here we investigated candidate intracellular mechanisms that may facilitate the intracellular targeting of Commissureless and Roundabout within the soma of commissural neurons. Using modified forms of Commissureless or Rabs we show that neither ubiquitination nor Rab activity are necessary for the intracellular targeting of Commissureless. In addition we reveal that axon outgrowth of many populations of neurons within the Drosophila central nervous system is also independent of Rab activity.
format Online
Article
Text
id pubmed-3655966
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36559662013-05-21 Commissureless Regulation of Axon Outgrowth across the Midline Is Independent of Rab Function van den Brink, Daan M. Banerji, Oishik Tear, Guy PLoS One Research Article Nervous system function requires that neurons within neural circuits are connected together precisely. These connections form during the process of axon guidance whereby each neuron extends an axon that migrates, often large distances, through a complex environment to reach its synaptic target. This task can be simplified by utilising intermediate targets to divide the route into smaller sections. This requires that axons adapt their behaviour as they migrate towards and away from intermediate targets. In the central nervous system the midline acts as an intermediate target for commissural axons. In Drosophila commissural axons switch from attraction towards to extension away from the midline by regulating the levels of the Roundabout receptor on their cell surface. This is achieved by Commissureless which directs Roundabout to an intracellular compartment in the soma prior to reaching the midline. Once across the midline Roundabout is allowed to reach the surface and acts as a receptor for the repellent ligand Slit that is secreted by cells at the midline. Here we investigated candidate intracellular mechanisms that may facilitate the intracellular targeting of Commissureless and Roundabout within the soma of commissural neurons. Using modified forms of Commissureless or Rabs we show that neither ubiquitination nor Rab activity are necessary for the intracellular targeting of Commissureless. In addition we reveal that axon outgrowth of many populations of neurons within the Drosophila central nervous system is also independent of Rab activity. Public Library of Science 2013-05-16 /pmc/articles/PMC3655966/ /pubmed/23696892 http://dx.doi.org/10.1371/journal.pone.0064427 Text en © 2013 van den Brink et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
van den Brink, Daan M.
Banerji, Oishik
Tear, Guy
Commissureless Regulation of Axon Outgrowth across the Midline Is Independent of Rab Function
title Commissureless Regulation of Axon Outgrowth across the Midline Is Independent of Rab Function
title_full Commissureless Regulation of Axon Outgrowth across the Midline Is Independent of Rab Function
title_fullStr Commissureless Regulation of Axon Outgrowth across the Midline Is Independent of Rab Function
title_full_unstemmed Commissureless Regulation of Axon Outgrowth across the Midline Is Independent of Rab Function
title_short Commissureless Regulation of Axon Outgrowth across the Midline Is Independent of Rab Function
title_sort commissureless regulation of axon outgrowth across the midline is independent of rab function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655966/
https://www.ncbi.nlm.nih.gov/pubmed/23696892
http://dx.doi.org/10.1371/journal.pone.0064427
work_keys_str_mv AT vandenbrinkdaanm commissurelessregulationofaxonoutgrowthacrossthemidlineisindependentofrabfunction
AT banerjioishik commissurelessregulationofaxonoutgrowthacrossthemidlineisindependentofrabfunction
AT tearguy commissurelessregulationofaxonoutgrowthacrossthemidlineisindependentofrabfunction