Cargando…
Mapping Gene Expression in Excitatory Neurons during Hippocampal Late-Phase Long-Term Potentiation
The persistence of long-lasting changes in synaptic connectivity that underlie long-term memory require new RNA and protein synthesis. To elucidate the temporal pattern of gene expression that gives rise to long-lasting neuronal plasticity, we analyzed differentially-expressed (DE) RNAs in mouse hip...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319997/ https://www.ncbi.nlm.nih.gov/pubmed/28275336 http://dx.doi.org/10.3389/fnmol.2017.00039 |
_version_ | 1782509453375963136 |
---|---|
author | Chen, Patrick B. Kawaguchi, Riki Blum, Charles Achiro, Jennifer M. Coppola, Giovanni O'Dell, Thomas J. Martin, Kelsey C. |
author_facet | Chen, Patrick B. Kawaguchi, Riki Blum, Charles Achiro, Jennifer M. Coppola, Giovanni O'Dell, Thomas J. Martin, Kelsey C. |
author_sort | Chen, Patrick B. |
collection | PubMed |
description | The persistence of long-lasting changes in synaptic connectivity that underlie long-term memory require new RNA and protein synthesis. To elucidate the temporal pattern of gene expression that gives rise to long-lasting neuronal plasticity, we analyzed differentially-expressed (DE) RNAs in mouse hippocampal slices following induction of late phase long-term potentiation (L-LTP) specifically within pyramidal excitatory neurons using Translating Ribosome Affinity Purification RNA sequencing (TRAP-seq). We detected time-dependent changes in up- and down-regulated ribosome-associated mRNAs over 2 h following L-LTP induction, with minimal overlap of DE transcripts between time points. TRAP-seq revealed greater numbers of DE transcripts and magnitudes of LTP-induced changes than RNA-seq of all cell types in the hippocampus. Neuron-enriched transcripts had greater changes at the ribosome-loading level than the total RNA level, while RNA-seq identified many non-neuronal DE mRNAs. Our results highlight the importance of considering both time course and cell-type specificity in activity-dependent gene expression during memory formation. |
format | Online Article Text |
id | pubmed-5319997 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-53199972017-03-08 Mapping Gene Expression in Excitatory Neurons during Hippocampal Late-Phase Long-Term Potentiation Chen, Patrick B. Kawaguchi, Riki Blum, Charles Achiro, Jennifer M. Coppola, Giovanni O'Dell, Thomas J. Martin, Kelsey C. Front Mol Neurosci Neuroscience The persistence of long-lasting changes in synaptic connectivity that underlie long-term memory require new RNA and protein synthesis. To elucidate the temporal pattern of gene expression that gives rise to long-lasting neuronal plasticity, we analyzed differentially-expressed (DE) RNAs in mouse hippocampal slices following induction of late phase long-term potentiation (L-LTP) specifically within pyramidal excitatory neurons using Translating Ribosome Affinity Purification RNA sequencing (TRAP-seq). We detected time-dependent changes in up- and down-regulated ribosome-associated mRNAs over 2 h following L-LTP induction, with minimal overlap of DE transcripts between time points. TRAP-seq revealed greater numbers of DE transcripts and magnitudes of LTP-induced changes than RNA-seq of all cell types in the hippocampus. Neuron-enriched transcripts had greater changes at the ribosome-loading level than the total RNA level, while RNA-seq identified many non-neuronal DE mRNAs. Our results highlight the importance of considering both time course and cell-type specificity in activity-dependent gene expression during memory formation. Frontiers Media S.A. 2017-02-22 /pmc/articles/PMC5319997/ /pubmed/28275336 http://dx.doi.org/10.3389/fnmol.2017.00039 Text en Copyright © 2017 Chen, Kawaguchi, Blum, Achiro, Coppola, O'Dell and Martin. 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 Chen, Patrick B. Kawaguchi, Riki Blum, Charles Achiro, Jennifer M. Coppola, Giovanni O'Dell, Thomas J. Martin, Kelsey C. Mapping Gene Expression in Excitatory Neurons during Hippocampal Late-Phase Long-Term Potentiation |
title | Mapping Gene Expression in Excitatory Neurons during Hippocampal Late-Phase Long-Term Potentiation |
title_full | Mapping Gene Expression in Excitatory Neurons during Hippocampal Late-Phase Long-Term Potentiation |
title_fullStr | Mapping Gene Expression in Excitatory Neurons during Hippocampal Late-Phase Long-Term Potentiation |
title_full_unstemmed | Mapping Gene Expression in Excitatory Neurons during Hippocampal Late-Phase Long-Term Potentiation |
title_short | Mapping Gene Expression in Excitatory Neurons during Hippocampal Late-Phase Long-Term Potentiation |
title_sort | mapping gene expression in excitatory neurons during hippocampal late-phase long-term potentiation |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5319997/ https://www.ncbi.nlm.nih.gov/pubmed/28275336 http://dx.doi.org/10.3389/fnmol.2017.00039 |
work_keys_str_mv | AT chenpatrickb mappinggeneexpressioninexcitatoryneuronsduringhippocampallatephaselongtermpotentiation AT kawaguchiriki mappinggeneexpressioninexcitatoryneuronsduringhippocampallatephaselongtermpotentiation AT blumcharles mappinggeneexpressioninexcitatoryneuronsduringhippocampallatephaselongtermpotentiation AT achirojenniferm mappinggeneexpressioninexcitatoryneuronsduringhippocampallatephaselongtermpotentiation AT coppolagiovanni mappinggeneexpressioninexcitatoryneuronsduringhippocampallatephaselongtermpotentiation AT odellthomasj mappinggeneexpressioninexcitatoryneuronsduringhippocampallatephaselongtermpotentiation AT martinkelseyc mappinggeneexpressioninexcitatoryneuronsduringhippocampallatephaselongtermpotentiation |