Evidence map›Paper›PMID 32860876›Full record

ArticleProgress in neurobiology2021

Uncovering memory-related gene expression in contextual fear conditioning using ribosome profiling.

Konstanze Simbriger, Inês S Amorim, Gilliard Lach, Kleanthi Chalkiadaki, Stella Kouloulia, Seyed Mehdi Jafarnejad, Arkady Khoutorsky, Christos G Gkogkas

Open access · hybridAbstract read
In one paragraph

Article in Progress in neurobiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.5field-weighted citation impact, top 41% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 2 countries.

Konstanze SimbrigerCentre for Discovery Brain Sciences, University of Edinburgh and Patrick Wild Centre and Simons Initiative for the Developing Brain, University of Edinburgh, EH8 9XD, Edinburgh, Scotland, UK.
Inês S AmorimCentre for Discovery Brain Sciences, University of Edinburgh and Patrick Wild Centre and Simons Initiative for the Developing Brain, University of Edinburgh, EH8 9XD, Edinburgh, Scotland, UK.
Gilliard LachCentre for Discovery Brain Sciences, University of Edinburgh and Patrick Wild Centre and Simons Initiative for the Developing Brain, University of Edinburgh, EH8 9XD, Edinburgh, Scotland, UK.
Kleanthi ChalkiadakiCentre for Discovery Brain Sciences, University of Edinburgh and Patrick Wild Centre and Simons Initiative for the Developing Brain, University of Edinburgh, EH8 9XD, Edinburgh, Scotland, UK.
Stella KoulouliaCentre for Discovery Brain Sciences, University of Edinburgh and Patrick Wild Centre and Simons Initiative for the Developing Brain, University of Edinburgh, EH8 9XD, Edinburgh, Scotland, UK.
Seyed Mehdi JafarnejadPatrick G. Johnston Centre for Cancer Research and Cell Biology, The Queen's University of Belfast, BT9 7AE Belfast, Northern Ireland, UK. Electronic address: sm.jafarnejad@qub.ac.uk.
Arkady KhoutorskyDepartment of Anesthesia, Faculty of Dentistry and Alan Edwards Centre for Research on Pain, McGill University, H3A 0G1, Montréal, QC, Canada. Electronic address: arkady.khoutorsky@mcgill.ca.
Christos G GkogkasCentre for Discovery Brain Sciences, University of Edinburgh and Patrick Wild Centre and Simons Initiative for the Developing Brain, University of Edinburgh, EH8 9XD, Edinburgh, Scotland, UK. Electronic address: christos.gkogkas@ed.ac.uk.
Simons Initiative for the Developing BrainMcGill University Health Centre · CAQueen's University Belfast · GB

Funding

Wellcome TrustWellcome Trust 107687/Z/15/Z
6 · The paper itself

Abstract

Contextual fear conditioning (CFC) in rodents is the most widely used behavioural paradigm in neuroscience research to elucidate the neurobiological mechanisms underlying learning and memory. It is based on the pairing of an aversive unconditioned stimulus (US; e.g. mild footshock) with a neutral conditioned stimulus (CS; e.g. context of the test chamber) in order to acquire associative long-term memory (LTM), which persists for days and even months. Using genome-wide analysis, several studies have generated lists of genes modulated in response to CFC in an attempt to identify the "memory genes", which orchestrate memory formation. Yet, most studies use naïve animals as a baseline for assessing gene-expression changes, while only few studies have examined the effect of the US alone, without pairing to context, using genome-wide analysis of gene-expression. Herein, using the ribosome profiling methodology, we show that in male mice an immediate shock, which does not lead to LTM formation, elicits pervasive translational and transcriptional changes in the expression of Immediate Early Genes (IEGs) in dorsal hippocampus (such as Fos and Arc), a fact which has been disregarded by the majority of CFC studies. By removing the effect of the immediate shock, we identify and validate a new set of genes, which are translationally and transcriptionally responsive to the association of context-to-footshock in CFC, and thus constitute salient "memory genes".

Indexed as

FearAnimalsConditioning, ClassicalGene ExpressionHippocampusMaleMiceRibosomesFear conditioningMemoryTranslational profiling

Identifiers

PMID32860876
PMCPMC7859833
OpenAlexW3080535672

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.