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Neurexin directs partner-specific synaptic connectivity in C. elegans

In neural circuits, individual neurons often make projections onto multiple postsynaptic partners. Here, we investigate molecular mechanisms by which these divergent connections are generated, using dyadic synapses in C. elegans as a model. We report that C. elegans nrx-1/neurexin directs divergent...

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Autores principales: Philbrook, Alison, Ramachandran, Shankar, Lambert, Christopher M, Oliver, Devyn, Florman, Jeremy, Alkema, Mark J, Lemons, Michele, Francis, Michael M
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057746/
https://www.ncbi.nlm.nih.gov/pubmed/30039797
http://dx.doi.org/10.7554/eLife.35692
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author Philbrook, Alison
Ramachandran, Shankar
Lambert, Christopher M
Oliver, Devyn
Florman, Jeremy
Alkema, Mark J
Lemons, Michele
Francis, Michael M
author_facet Philbrook, Alison
Ramachandran, Shankar
Lambert, Christopher M
Oliver, Devyn
Florman, Jeremy
Alkema, Mark J
Lemons, Michele
Francis, Michael M
author_sort Philbrook, Alison
collection PubMed
description In neural circuits, individual neurons often make projections onto multiple postsynaptic partners. Here, we investigate molecular mechanisms by which these divergent connections are generated, using dyadic synapses in C. elegans as a model. We report that C. elegans nrx-1/neurexin directs divergent connectivity through differential actions at synapses with partnering neurons and muscles. We show that cholinergic outputs onto neurons are, unexpectedly, located at previously undefined spine-like protrusions from GABAergic dendrites. Both these spine-like features and cholinergic receptor clustering are strikingly disrupted in the absence of nrx-1. Excitatory transmission onto GABAergic neurons, but not neuromuscular transmission, is also disrupted. Our data indicate that NRX-1 located at presynaptic sites specifically directs postsynaptic development in GABAergic neurons. Our findings provide evidence that individual neurons can direct differential patterns of connectivity with their post-synaptic partners through partner-specific utilization of synaptic organizers, offering a novel view into molecular control of divergent connectivity.
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spelling pubmed-60577462018-07-25 Neurexin directs partner-specific synaptic connectivity in C. elegans Philbrook, Alison Ramachandran, Shankar Lambert, Christopher M Oliver, Devyn Florman, Jeremy Alkema, Mark J Lemons, Michele Francis, Michael M eLife Neuroscience In neural circuits, individual neurons often make projections onto multiple postsynaptic partners. Here, we investigate molecular mechanisms by which these divergent connections are generated, using dyadic synapses in C. elegans as a model. We report that C. elegans nrx-1/neurexin directs divergent connectivity through differential actions at synapses with partnering neurons and muscles. We show that cholinergic outputs onto neurons are, unexpectedly, located at previously undefined spine-like protrusions from GABAergic dendrites. Both these spine-like features and cholinergic receptor clustering are strikingly disrupted in the absence of nrx-1. Excitatory transmission onto GABAergic neurons, but not neuromuscular transmission, is also disrupted. Our data indicate that NRX-1 located at presynaptic sites specifically directs postsynaptic development in GABAergic neurons. Our findings provide evidence that individual neurons can direct differential patterns of connectivity with their post-synaptic partners through partner-specific utilization of synaptic organizers, offering a novel view into molecular control of divergent connectivity. eLife Sciences Publications, Ltd 2018-07-24 /pmc/articles/PMC6057746/ /pubmed/30039797 http://dx.doi.org/10.7554/eLife.35692 Text en © 2018, Philbrook et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Neuroscience
Philbrook, Alison
Ramachandran, Shankar
Lambert, Christopher M
Oliver, Devyn
Florman, Jeremy
Alkema, Mark J
Lemons, Michele
Francis, Michael M
Neurexin directs partner-specific synaptic connectivity in C. elegans
title Neurexin directs partner-specific synaptic connectivity in C. elegans
title_full Neurexin directs partner-specific synaptic connectivity in C. elegans
title_fullStr Neurexin directs partner-specific synaptic connectivity in C. elegans
title_full_unstemmed Neurexin directs partner-specific synaptic connectivity in C. elegans
title_short Neurexin directs partner-specific synaptic connectivity in C. elegans
title_sort neurexin directs partner-specific synaptic connectivity in c. elegans
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057746/
https://www.ncbi.nlm.nih.gov/pubmed/30039797
http://dx.doi.org/10.7554/eLife.35692
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