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Localization and local translation of Arc/Arg3.1 mRNA at synapses: some observations and paradoxes

Arc is a unique immediate early gene whose expression is induced as synapses are being modified during learning. The uniqueness comes from the fact that newly synthesized Arc mRNA is rapidly transported throughout dendrites where it localizes near synapses that were recently activated. Here, we summ...

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Autores principales: Steward, Oswald, Farris, Shannon, Pirbhoy, Patricia S., Darnell, Jennifer, Driesche, Sarah J. Van
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290588/
https://www.ncbi.nlm.nih.gov/pubmed/25628532
http://dx.doi.org/10.3389/fnmol.2014.00101
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author Steward, Oswald
Farris, Shannon
Pirbhoy, Patricia S.
Darnell, Jennifer
Driesche, Sarah J. Van
author_facet Steward, Oswald
Farris, Shannon
Pirbhoy, Patricia S.
Darnell, Jennifer
Driesche, Sarah J. Van
author_sort Steward, Oswald
collection PubMed
description Arc is a unique immediate early gene whose expression is induced as synapses are being modified during learning. The uniqueness comes from the fact that newly synthesized Arc mRNA is rapidly transported throughout dendrites where it localizes near synapses that were recently activated. Here, we summarize aspects of Arc mRNA translation in dendrites in vivo, focusing especially on features of its expression that are paradoxical or that donot fit in with current models of how Arc protein operates. Findings from in vivo studies that donot quite fit include: (1) Following induction of LTP in vivo, Arc mRNA and protein localize near active synapses, but are also distributed throughout dendrites. In contrast, Arc mRNA localizes selectively near active synapses when stimulation is continued as Arc mRNA is transported into dendrites; (2) Strong induction of Arc expression as a result of a seizure does not lead to a rundown of synaptic efficacy in vivo as would be predicted by the hypothesis that high levels of Arc cause glutamate receptor endocytosis and LTD. (3) Arc protein is synthesized in the perinuclear cytoplasm rapidly after transcriptional activation, indicating that at least a pool of Arc mRNA is not translationally repressed to allow for dendritic delivery; (4) Increases in Arc mRNA in dendrites are not paralleled by increases in levels of exon junction complex (EJC) proteins. These results of studies of mRNA trafficking in neurons in vivo provide a new perspective on the possible roles of Arc in activity-dependent synaptic modifications.
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spelling pubmed-42905882015-01-27 Localization and local translation of Arc/Arg3.1 mRNA at synapses: some observations and paradoxes Steward, Oswald Farris, Shannon Pirbhoy, Patricia S. Darnell, Jennifer Driesche, Sarah J. Van Front Mol Neurosci Neuroscience Arc is a unique immediate early gene whose expression is induced as synapses are being modified during learning. The uniqueness comes from the fact that newly synthesized Arc mRNA is rapidly transported throughout dendrites where it localizes near synapses that were recently activated. Here, we summarize aspects of Arc mRNA translation in dendrites in vivo, focusing especially on features of its expression that are paradoxical or that donot fit in with current models of how Arc protein operates. Findings from in vivo studies that donot quite fit include: (1) Following induction of LTP in vivo, Arc mRNA and protein localize near active synapses, but are also distributed throughout dendrites. In contrast, Arc mRNA localizes selectively near active synapses when stimulation is continued as Arc mRNA is transported into dendrites; (2) Strong induction of Arc expression as a result of a seizure does not lead to a rundown of synaptic efficacy in vivo as would be predicted by the hypothesis that high levels of Arc cause glutamate receptor endocytosis and LTD. (3) Arc protein is synthesized in the perinuclear cytoplasm rapidly after transcriptional activation, indicating that at least a pool of Arc mRNA is not translationally repressed to allow for dendritic delivery; (4) Increases in Arc mRNA in dendrites are not paralleled by increases in levels of exon junction complex (EJC) proteins. These results of studies of mRNA trafficking in neurons in vivo provide a new perspective on the possible roles of Arc in activity-dependent synaptic modifications. Frontiers Media S.A. 2015-01-12 /pmc/articles/PMC4290588/ /pubmed/25628532 http://dx.doi.org/10.3389/fnmol.2014.00101 Text en Copyright © 2015 Steward, Farris, Pirbhoy, Darnell and Van Driesche. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Steward, Oswald
Farris, Shannon
Pirbhoy, Patricia S.
Darnell, Jennifer
Driesche, Sarah J. Van
Localization and local translation of Arc/Arg3.1 mRNA at synapses: some observations and paradoxes
title Localization and local translation of Arc/Arg3.1 mRNA at synapses: some observations and paradoxes
title_full Localization and local translation of Arc/Arg3.1 mRNA at synapses: some observations and paradoxes
title_fullStr Localization and local translation of Arc/Arg3.1 mRNA at synapses: some observations and paradoxes
title_full_unstemmed Localization and local translation of Arc/Arg3.1 mRNA at synapses: some observations and paradoxes
title_short Localization and local translation of Arc/Arg3.1 mRNA at synapses: some observations and paradoxes
title_sort localization and local translation of arc/arg3.1 mrna at synapses: some observations and paradoxes
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4290588/
https://www.ncbi.nlm.nih.gov/pubmed/25628532
http://dx.doi.org/10.3389/fnmol.2014.00101
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