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Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation

Memory consolidation involves discrete patterns of transcriptional events in the hippocampus. Despite the emergence of single-cell transcriptomic profiling techniques, mapping the transcriptomic signature across subregions of the hippocampus has remained challenging. Here, we utilized unbiased spati...

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Autores principales: Vanrobaeys, Yann, Mukherjee, Utsav, Langmack, Lucy, Beyer, Stacy E., Bahl, Ethan, Lin, Li-Chun, Michaelson, Jacob J., Abel, Ted, Chatterjee, Snehajyoti
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541893/
https://www.ncbi.nlm.nih.gov/pubmed/37773230
http://dx.doi.org/10.1038/s41467-023-41715-7
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author Vanrobaeys, Yann
Mukherjee, Utsav
Langmack, Lucy
Beyer, Stacy E.
Bahl, Ethan
Lin, Li-Chun
Michaelson, Jacob J.
Abel, Ted
Chatterjee, Snehajyoti
author_facet Vanrobaeys, Yann
Mukherjee, Utsav
Langmack, Lucy
Beyer, Stacy E.
Bahl, Ethan
Lin, Li-Chun
Michaelson, Jacob J.
Abel, Ted
Chatterjee, Snehajyoti
author_sort Vanrobaeys, Yann
collection PubMed
description Memory consolidation involves discrete patterns of transcriptional events in the hippocampus. Despite the emergence of single-cell transcriptomic profiling techniques, mapping the transcriptomic signature across subregions of the hippocampus has remained challenging. Here, we utilized unbiased spatial sequencing to delineate transcriptome-wide gene expression changes across subregions of the dorsal hippocampus of male mice following learning. We find that each subregion of the hippocampus exhibits distinct yet overlapping transcriptomic signatures. The CA1 region exhibited increased expression of genes related to transcriptional regulation, while the DG showed upregulation of genes associated with protein folding. Importantly, our approach enabled us to define the transcriptomic signature of learning within two less-defined hippocampal subregions, CA1 stratum radiatum, and oriens. We demonstrated that CA1 subregion-specific expression of a transcription factor subfamily has a critical functional role in the consolidation of long-term memory. This work demonstrates the power of spatial molecular approaches to reveal simultaneous transcriptional events across the hippocampus during memory consolidation.
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spelling pubmed-105418932023-10-02 Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation Vanrobaeys, Yann Mukherjee, Utsav Langmack, Lucy Beyer, Stacy E. Bahl, Ethan Lin, Li-Chun Michaelson, Jacob J. Abel, Ted Chatterjee, Snehajyoti Nat Commun Article Memory consolidation involves discrete patterns of transcriptional events in the hippocampus. Despite the emergence of single-cell transcriptomic profiling techniques, mapping the transcriptomic signature across subregions of the hippocampus has remained challenging. Here, we utilized unbiased spatial sequencing to delineate transcriptome-wide gene expression changes across subregions of the dorsal hippocampus of male mice following learning. We find that each subregion of the hippocampus exhibits distinct yet overlapping transcriptomic signatures. The CA1 region exhibited increased expression of genes related to transcriptional regulation, while the DG showed upregulation of genes associated with protein folding. Importantly, our approach enabled us to define the transcriptomic signature of learning within two less-defined hippocampal subregions, CA1 stratum radiatum, and oriens. We demonstrated that CA1 subregion-specific expression of a transcription factor subfamily has a critical functional role in the consolidation of long-term memory. This work demonstrates the power of spatial molecular approaches to reveal simultaneous transcriptional events across the hippocampus during memory consolidation. Nature Publishing Group UK 2023-09-29 /pmc/articles/PMC10541893/ /pubmed/37773230 http://dx.doi.org/10.1038/s41467-023-41715-7 Text en © The Author(s) 2023 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
Vanrobaeys, Yann
Mukherjee, Utsav
Langmack, Lucy
Beyer, Stacy E.
Bahl, Ethan
Lin, Li-Chun
Michaelson, Jacob J.
Abel, Ted
Chatterjee, Snehajyoti
Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation
title Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation
title_full Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation
title_fullStr Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation
title_full_unstemmed Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation
title_short Mapping the spatial transcriptomic signature of the hippocampus during memory consolidation
title_sort mapping the spatial transcriptomic signature of the hippocampus during memory consolidation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10541893/
https://www.ncbi.nlm.nih.gov/pubmed/37773230
http://dx.doi.org/10.1038/s41467-023-41715-7
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