Cargando…

RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex

The stable formation of remote fear memories is thought to require neuronal gene induction in cortical ensembles that are activated during learning. However, the set of genes expressed specifically in these activated ensembles is not known; knowledge of such transcriptional profiles may offer insigh...

Descripción completa

Detalles Bibliográficos
Autores principales: Cho, Jin-Hyung, Huang, Ben S., Gray, Jesse M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997356/
https://www.ncbi.nlm.nih.gov/pubmed/27557751
http://dx.doi.org/10.1038/srep31753
_version_ 1782449755802042368
author Cho, Jin-Hyung
Huang, Ben S.
Gray, Jesse M.
author_facet Cho, Jin-Hyung
Huang, Ben S.
Gray, Jesse M.
author_sort Cho, Jin-Hyung
collection PubMed
description The stable formation of remote fear memories is thought to require neuronal gene induction in cortical ensembles that are activated during learning. However, the set of genes expressed specifically in these activated ensembles is not known; knowledge of such transcriptional profiles may offer insights into the molecular program underlying stable memory formation. Here we use RNA-Seq to identify genes whose expression is enriched in activated cortical ensembles labeled during associative fear learning. We first establish that mouse temporal association cortex (TeA) is required for remote recall of auditory fear memories. We then perform RNA-Seq in TeA neurons that are labeled by the activity reporter Arc-dVenus during learning. We identify 944 genes with enriched expression in Arc-dVenus+ neurons. These genes include markers of L2/3, L5b, and L6 excitatory neurons but not glial or inhibitory markers, confirming Arc-dVenus to be an excitatory neuron-specific but non-layer-specific activity reporter. Cross comparisons to other transcriptional profiles show that 125 of the enriched genes are also activity-regulated in vitro or induced by visual stimulus in the visual cortex, suggesting that they may be induced generally in the cortex in an experience-dependent fashion. Prominent among the enriched genes are those encoding potassium channels that down-regulate neuronal activity, suggesting the possibility that part of the molecular program induced by fear conditioning may initiate homeostatic plasticity.
format Online
Article
Text
id pubmed-4997356
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-49973562016-09-01 RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex Cho, Jin-Hyung Huang, Ben S. Gray, Jesse M. Sci Rep Article The stable formation of remote fear memories is thought to require neuronal gene induction in cortical ensembles that are activated during learning. However, the set of genes expressed specifically in these activated ensembles is not known; knowledge of such transcriptional profiles may offer insights into the molecular program underlying stable memory formation. Here we use RNA-Seq to identify genes whose expression is enriched in activated cortical ensembles labeled during associative fear learning. We first establish that mouse temporal association cortex (TeA) is required for remote recall of auditory fear memories. We then perform RNA-Seq in TeA neurons that are labeled by the activity reporter Arc-dVenus during learning. We identify 944 genes with enriched expression in Arc-dVenus+ neurons. These genes include markers of L2/3, L5b, and L6 excitatory neurons but not glial or inhibitory markers, confirming Arc-dVenus to be an excitatory neuron-specific but non-layer-specific activity reporter. Cross comparisons to other transcriptional profiles show that 125 of the enriched genes are also activity-regulated in vitro or induced by visual stimulus in the visual cortex, suggesting that they may be induced generally in the cortex in an experience-dependent fashion. Prominent among the enriched genes are those encoding potassium channels that down-regulate neuronal activity, suggesting the possibility that part of the molecular program induced by fear conditioning may initiate homeostatic plasticity. Nature Publishing Group 2016-08-25 /pmc/articles/PMC4997356/ /pubmed/27557751 http://dx.doi.org/10.1038/srep31753 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Cho, Jin-Hyung
Huang, Ben S.
Gray, Jesse M.
RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex
title RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex
title_full RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex
title_fullStr RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex
title_full_unstemmed RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex
title_short RNA sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex
title_sort rna sequencing from neural ensembles activated during fear conditioning in the mouse temporal association cortex
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4997356/
https://www.ncbi.nlm.nih.gov/pubmed/27557751
http://dx.doi.org/10.1038/srep31753
work_keys_str_mv AT chojinhyung rnasequencingfromneuralensemblesactivatedduringfearconditioninginthemousetemporalassociationcortex
AT huangbens rnasequencingfromneuralensemblesactivatedduringfearconditioninginthemousetemporalassociationcortex
AT grayjessem rnasequencingfromneuralensemblesactivatedduringfearconditioninginthemousetemporalassociationcortex