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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2018
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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. |
format | Online Article Text |
id | pubmed-6057746 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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