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miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development

SNAP-25 is a core component of the trimeric SNARE complex mediating vesicle exocytosis during membrane addition for neuronal growth, neuropeptide/growth factor secretion, and neurotransmitter release during synaptic transmission. Here, we report a novel microRNA mechanism of SNAP-25 regulation contr...

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Autores principales: Wei, Chunyao, Thatcher, Elizabeth J., Olena, Abigail F., Cha, Diana J., Perdigoto, Ana L., Marshall, Andrew F., Carter, Bruce D., Broadie, Kendal, Patton, James G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581580/
https://www.ncbi.nlm.nih.gov/pubmed/23451149
http://dx.doi.org/10.1371/journal.pone.0057080
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author Wei, Chunyao
Thatcher, Elizabeth J.
Olena, Abigail F.
Cha, Diana J.
Perdigoto, Ana L.
Marshall, Andrew F.
Carter, Bruce D.
Broadie, Kendal
Patton, James G.
author_facet Wei, Chunyao
Thatcher, Elizabeth J.
Olena, Abigail F.
Cha, Diana J.
Perdigoto, Ana L.
Marshall, Andrew F.
Carter, Bruce D.
Broadie, Kendal
Patton, James G.
author_sort Wei, Chunyao
collection PubMed
description SNAP-25 is a core component of the trimeric SNARE complex mediating vesicle exocytosis during membrane addition for neuronal growth, neuropeptide/growth factor secretion, and neurotransmitter release during synaptic transmission. Here, we report a novel microRNA mechanism of SNAP-25 regulation controlling motor neuron development, neurosecretion, synaptic activity, and movement in zebrafish. Loss of miR-153 causes overexpression of SNAP-25 and consequent hyperactive movement in early zebrafish embryos. Conversely, overexpression of miR-153 causes SNAP-25 down regulation resulting in near complete paralysis, mimicking the effects of treatment with Botulinum neurotoxin. miR-153-dependent changes in synaptic activity at the neuromuscular junction are consistent with the observed movement defects. Underlying the movement defects, perturbation of miR-153 function causes dramatic developmental changes in motor neuron patterning and branching. Together, our results indicate that precise control of SNAP-25 expression by miR-153 is critically important for proper neuronal patterning as well as neurotransmission.
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spelling pubmed-35815802013-02-28 miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development Wei, Chunyao Thatcher, Elizabeth J. Olena, Abigail F. Cha, Diana J. Perdigoto, Ana L. Marshall, Andrew F. Carter, Bruce D. Broadie, Kendal Patton, James G. PLoS One Research Article SNAP-25 is a core component of the trimeric SNARE complex mediating vesicle exocytosis during membrane addition for neuronal growth, neuropeptide/growth factor secretion, and neurotransmitter release during synaptic transmission. Here, we report a novel microRNA mechanism of SNAP-25 regulation controlling motor neuron development, neurosecretion, synaptic activity, and movement in zebrafish. Loss of miR-153 causes overexpression of SNAP-25 and consequent hyperactive movement in early zebrafish embryos. Conversely, overexpression of miR-153 causes SNAP-25 down regulation resulting in near complete paralysis, mimicking the effects of treatment with Botulinum neurotoxin. miR-153-dependent changes in synaptic activity at the neuromuscular junction are consistent with the observed movement defects. Underlying the movement defects, perturbation of miR-153 function causes dramatic developmental changes in motor neuron patterning and branching. Together, our results indicate that precise control of SNAP-25 expression by miR-153 is critically important for proper neuronal patterning as well as neurotransmission. Public Library of Science 2013-02-25 /pmc/articles/PMC3581580/ /pubmed/23451149 http://dx.doi.org/10.1371/journal.pone.0057080 Text en © 2013 Wei 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
Wei, Chunyao
Thatcher, Elizabeth J.
Olena, Abigail F.
Cha, Diana J.
Perdigoto, Ana L.
Marshall, Andrew F.
Carter, Bruce D.
Broadie, Kendal
Patton, James G.
miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development
title miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development
title_full miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development
title_fullStr miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development
title_full_unstemmed miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development
title_short miR-153 Regulates SNAP-25, Synaptic Transmission, and Neuronal Development
title_sort mir-153 regulates snap-25, synaptic transmission, and neuronal development
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3581580/
https://www.ncbi.nlm.nih.gov/pubmed/23451149
http://dx.doi.org/10.1371/journal.pone.0057080
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