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Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses

mRNA transport restricts translation to specific subcellular locations, which is the basis for many cellular functions. However, the precise process of mRNA sorting to synapses in neurons remains elusive. Here we use Rgs4 mRNA to investigate 3′-UTR-dependent transport by MS2 live-cell imaging. The m...

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Autores principales: Bauer, Karl E., Segura, Inmaculada, Gaspar, Imre, Scheuss, Volker, Illig, Christin, Ammer, Georg, Hutten, Saskia, Basyuk, Eugénia, Fernández-Moya, Sandra M., Ehses, Janina, Bertrand, Edouard, Kiebler, Michael A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639396/
https://www.ncbi.nlm.nih.gov/pubmed/31320644
http://dx.doi.org/10.1038/s41467-019-11123-x
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author Bauer, Karl E.
Segura, Inmaculada
Gaspar, Imre
Scheuss, Volker
Illig, Christin
Ammer, Georg
Hutten, Saskia
Basyuk, Eugénia
Fernández-Moya, Sandra M.
Ehses, Janina
Bertrand, Edouard
Kiebler, Michael A.
author_facet Bauer, Karl E.
Segura, Inmaculada
Gaspar, Imre
Scheuss, Volker
Illig, Christin
Ammer, Georg
Hutten, Saskia
Basyuk, Eugénia
Fernández-Moya, Sandra M.
Ehses, Janina
Bertrand, Edouard
Kiebler, Michael A.
author_sort Bauer, Karl E.
collection PubMed
description mRNA transport restricts translation to specific subcellular locations, which is the basis for many cellular functions. However, the precise process of mRNA sorting to synapses in neurons remains elusive. Here we use Rgs4 mRNA to investigate 3′-UTR-dependent transport by MS2 live-cell imaging. The majority of observed RNA granules display 3′-UTR independent bidirectional transport in dendrites. Importantly, the Rgs4 3′-UTR causes an anterograde transport bias, which requires the Staufen2 protein. Moreover, the 3′-UTR mediates dynamic, sustained mRNA recruitment to synapses. Visualization at high temporal resolution enables us to show mRNA patrolling dendrites, allowing transient interaction with multiple synapses, in agreement with the sushi-belt model. Modulation of neuronal activity by either chemical silencing or local glutamate uncaging regulates both the 3′-UTR-dependent transport bias and synaptic recruitment. This dynamic and reversible mRNA recruitment to active synapses would allow translation and synaptic remodeling in a spatially and temporally adaptive manner.
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spelling pubmed-66393962019-07-22 Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses Bauer, Karl E. Segura, Inmaculada Gaspar, Imre Scheuss, Volker Illig, Christin Ammer, Georg Hutten, Saskia Basyuk, Eugénia Fernández-Moya, Sandra M. Ehses, Janina Bertrand, Edouard Kiebler, Michael A. Nat Commun Article mRNA transport restricts translation to specific subcellular locations, which is the basis for many cellular functions. However, the precise process of mRNA sorting to synapses in neurons remains elusive. Here we use Rgs4 mRNA to investigate 3′-UTR-dependent transport by MS2 live-cell imaging. The majority of observed RNA granules display 3′-UTR independent bidirectional transport in dendrites. Importantly, the Rgs4 3′-UTR causes an anterograde transport bias, which requires the Staufen2 protein. Moreover, the 3′-UTR mediates dynamic, sustained mRNA recruitment to synapses. Visualization at high temporal resolution enables us to show mRNA patrolling dendrites, allowing transient interaction with multiple synapses, in agreement with the sushi-belt model. Modulation of neuronal activity by either chemical silencing or local glutamate uncaging regulates both the 3′-UTR-dependent transport bias and synaptic recruitment. This dynamic and reversible mRNA recruitment to active synapses would allow translation and synaptic remodeling in a spatially and temporally adaptive manner. Nature Publishing Group UK 2019-07-18 /pmc/articles/PMC6639396/ /pubmed/31320644 http://dx.doi.org/10.1038/s41467-019-11123-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Bauer, Karl E.
Segura, Inmaculada
Gaspar, Imre
Scheuss, Volker
Illig, Christin
Ammer, Georg
Hutten, Saskia
Basyuk, Eugénia
Fernández-Moya, Sandra M.
Ehses, Janina
Bertrand, Edouard
Kiebler, Michael A.
Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses
title Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses
title_full Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses
title_fullStr Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses
title_full_unstemmed Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses
title_short Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses
title_sort live cell imaging reveals 3′-utr dependent mrna sorting to synapses
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6639396/
https://www.ncbi.nlm.nih.gov/pubmed/31320644
http://dx.doi.org/10.1038/s41467-019-11123-x
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