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The Coding and Small Non-coding Hippocampal Synaptic RNAome

Neurons are highly compartmentalized cells that depend on local protein synthesis. Messenger RNAs (mRNAs) have thus been detected in neuronal dendrites, and more recently in the pre- and postsynaptic compartments as well. Other RNA species such as microRNAs have also been described at synapses where...

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Autores principales: Epple, Robert, Krüger, Dennis, Berulava, Tea, Brehm, Gerrit, Ninov, Momchil, Islam, Rezaul, Köster, Sarah, Fischer, Andre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128755/
https://www.ncbi.nlm.nih.gov/pubmed/33569760
http://dx.doi.org/10.1007/s12035-021-02296-y
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author Epple, Robert
Krüger, Dennis
Berulava, Tea
Brehm, Gerrit
Ninov, Momchil
Islam, Rezaul
Köster, Sarah
Fischer, Andre
author_facet Epple, Robert
Krüger, Dennis
Berulava, Tea
Brehm, Gerrit
Ninov, Momchil
Islam, Rezaul
Köster, Sarah
Fischer, Andre
author_sort Epple, Robert
collection PubMed
description Neurons are highly compartmentalized cells that depend on local protein synthesis. Messenger RNAs (mRNAs) have thus been detected in neuronal dendrites, and more recently in the pre- and postsynaptic compartments as well. Other RNA species such as microRNAs have also been described at synapses where they are believed to control mRNA availability for local translation. A combined dataset analyzing the synaptic coding and non-coding RNAome via next-generation sequencing approaches is, however, still lacking. Here, we isolate synaptosomes from the hippocampus of young wild-type mice and provide the coding and non-coding synaptic RNAome. These data are complemented by a novel approach for analyzing the synaptic RNAome from primary hippocampal neurons grown in microfluidic chambers. Our data show that synaptic microRNAs control almost the entire synaptic mRNAome, and we identified several hub microRNAs. By combining the in vivo synaptosomal data with our novel microfluidic chamber system, our findings also support the hypothesis that part of the synaptic microRNAome may be supplied to neurons via astrocytes. Moreover, the microfluidic system is suitable for studying the dynamics of the synaptic RNAome in response to stimulation. In conclusion, our data provide a valuable resource and point to several important targets for further research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12035-021-02296-y.
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spelling pubmed-81287552021-05-24 The Coding and Small Non-coding Hippocampal Synaptic RNAome Epple, Robert Krüger, Dennis Berulava, Tea Brehm, Gerrit Ninov, Momchil Islam, Rezaul Köster, Sarah Fischer, Andre Mol Neurobiol Article Neurons are highly compartmentalized cells that depend on local protein synthesis. Messenger RNAs (mRNAs) have thus been detected in neuronal dendrites, and more recently in the pre- and postsynaptic compartments as well. Other RNA species such as microRNAs have also been described at synapses where they are believed to control mRNA availability for local translation. A combined dataset analyzing the synaptic coding and non-coding RNAome via next-generation sequencing approaches is, however, still lacking. Here, we isolate synaptosomes from the hippocampus of young wild-type mice and provide the coding and non-coding synaptic RNAome. These data are complemented by a novel approach for analyzing the synaptic RNAome from primary hippocampal neurons grown in microfluidic chambers. Our data show that synaptic microRNAs control almost the entire synaptic mRNAome, and we identified several hub microRNAs. By combining the in vivo synaptosomal data with our novel microfluidic chamber system, our findings also support the hypothesis that part of the synaptic microRNAome may be supplied to neurons via astrocytes. Moreover, the microfluidic system is suitable for studying the dynamics of the synaptic RNAome in response to stimulation. In conclusion, our data provide a valuable resource and point to several important targets for further research. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12035-021-02296-y. Springer US 2021-02-10 2021 /pmc/articles/PMC8128755/ /pubmed/33569760 http://dx.doi.org/10.1007/s12035-021-02296-y Text en © The Author(s) 2021, corrected publication 2021 https://creativecommons.org/licenses/by/4.0/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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Epple, Robert
Krüger, Dennis
Berulava, Tea
Brehm, Gerrit
Ninov, Momchil
Islam, Rezaul
Köster, Sarah
Fischer, Andre
The Coding and Small Non-coding Hippocampal Synaptic RNAome
title The Coding and Small Non-coding Hippocampal Synaptic RNAome
title_full The Coding and Small Non-coding Hippocampal Synaptic RNAome
title_fullStr The Coding and Small Non-coding Hippocampal Synaptic RNAome
title_full_unstemmed The Coding and Small Non-coding Hippocampal Synaptic RNAome
title_short The Coding and Small Non-coding Hippocampal Synaptic RNAome
title_sort coding and small non-coding hippocampal synaptic rnaome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128755/
https://www.ncbi.nlm.nih.gov/pubmed/33569760
http://dx.doi.org/10.1007/s12035-021-02296-y
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