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Learning-induced gene expression in the heads of two Nasonia species that differ in long-term memory formation

BACKGROUND: Cellular processes underlying memory formation are evolutionary conserved, but natural variation in memory dynamics between animal species or populations is common. The genetic basis of this fascinating phenomenon is poorly understood. Closely related species of Nasonia parasitic wasps d...

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Autores principales: Hoedjes, Katja M, Smid, Hans M, Schijlen, Elio GWM, Vet, Louise EM, van Vugt, Joke JFA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440501/
https://www.ncbi.nlm.nih.gov/pubmed/25888126
http://dx.doi.org/10.1186/s12864-015-1355-1
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author Hoedjes, Katja M
Smid, Hans M
Schijlen, Elio GWM
Vet, Louise EM
van Vugt, Joke JFA
author_facet Hoedjes, Katja M
Smid, Hans M
Schijlen, Elio GWM
Vet, Louise EM
van Vugt, Joke JFA
author_sort Hoedjes, Katja M
collection PubMed
description BACKGROUND: Cellular processes underlying memory formation are evolutionary conserved, but natural variation in memory dynamics between animal species or populations is common. The genetic basis of this fascinating phenomenon is poorly understood. Closely related species of Nasonia parasitic wasps differ in long-term memory (LTM) formation: N. vitripennis will form transcription-dependent LTM after a single conditioning trial, whereas the closely-related species N. giraulti will not. Genes that were differentially expressed (DE) after conditioning in N. vitripennis, but not in N. giraulti, were identified as candidate genes that may regulate LTM formation. RESULTS: RNA was collected from heads of both species before and immediately, 4 or 24 hours after conditioning, with 3 replicates per time point. It was sequenced strand-specifically, which allows distinguishing sense from antisense transcripts and improves the quality of expression analyses. We determined conditioning-induced DE compared to naïve controls for both species. These expression patterns were then analysed with GO enrichment analyses for each species and time point, which demonstrated an enrichment of signalling-related genes immediately after conditioning in N. vitripennis only. Analyses of known LTM genes and genes with an opposing expression pattern between the two species revealed additional candidate genes for the difference in LTM formation. These include genes from various signalling cascades, including several members of the Ras and PI3 kinase signalling pathways, and glutamate receptors. Interestingly, several other known LTM genes were exclusively differentially expressed in N. giraulti, which may indicate an LTM-inhibitory mechanism. Among the DE transcripts were also antisense transcripts. Furthermore, antisense transcripts aligning to a number of known memory genes were detected, which may have a role in regulating these genes. CONCLUSION: This study is the first to describe and compare expression patterns of both protein-coding and antisense transcripts, at different time points after conditioning, of two closely related animal species that differ in LTM formation. Several candidate genes that may regulate differences in LTM have been identified. This transcriptome analysis is a valuable resource for future in-depth studies to elucidate the role of candidate genes and antisense transcription in natural variation in LTM formation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1355-1) contains supplementary material, which is available to authorized users.
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spelling pubmed-44405012015-05-22 Learning-induced gene expression in the heads of two Nasonia species that differ in long-term memory formation Hoedjes, Katja M Smid, Hans M Schijlen, Elio GWM Vet, Louise EM van Vugt, Joke JFA BMC Genomics Research Article BACKGROUND: Cellular processes underlying memory formation are evolutionary conserved, but natural variation in memory dynamics between animal species or populations is common. The genetic basis of this fascinating phenomenon is poorly understood. Closely related species of Nasonia parasitic wasps differ in long-term memory (LTM) formation: N. vitripennis will form transcription-dependent LTM after a single conditioning trial, whereas the closely-related species N. giraulti will not. Genes that were differentially expressed (DE) after conditioning in N. vitripennis, but not in N. giraulti, were identified as candidate genes that may regulate LTM formation. RESULTS: RNA was collected from heads of both species before and immediately, 4 or 24 hours after conditioning, with 3 replicates per time point. It was sequenced strand-specifically, which allows distinguishing sense from antisense transcripts and improves the quality of expression analyses. We determined conditioning-induced DE compared to naïve controls for both species. These expression patterns were then analysed with GO enrichment analyses for each species and time point, which demonstrated an enrichment of signalling-related genes immediately after conditioning in N. vitripennis only. Analyses of known LTM genes and genes with an opposing expression pattern between the two species revealed additional candidate genes for the difference in LTM formation. These include genes from various signalling cascades, including several members of the Ras and PI3 kinase signalling pathways, and glutamate receptors. Interestingly, several other known LTM genes were exclusively differentially expressed in N. giraulti, which may indicate an LTM-inhibitory mechanism. Among the DE transcripts were also antisense transcripts. Furthermore, antisense transcripts aligning to a number of known memory genes were detected, which may have a role in regulating these genes. CONCLUSION: This study is the first to describe and compare expression patterns of both protein-coding and antisense transcripts, at different time points after conditioning, of two closely related animal species that differ in LTM formation. Several candidate genes that may regulate differences in LTM have been identified. This transcriptome analysis is a valuable resource for future in-depth studies to elucidate the role of candidate genes and antisense transcription in natural variation in LTM formation. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12864-015-1355-1) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-10 /pmc/articles/PMC4440501/ /pubmed/25888126 http://dx.doi.org/10.1186/s12864-015-1355-1 Text en © Hoedjes et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hoedjes, Katja M
Smid, Hans M
Schijlen, Elio GWM
Vet, Louise EM
van Vugt, Joke JFA
Learning-induced gene expression in the heads of two Nasonia species that differ in long-term memory formation
title Learning-induced gene expression in the heads of two Nasonia species that differ in long-term memory formation
title_full Learning-induced gene expression in the heads of two Nasonia species that differ in long-term memory formation
title_fullStr Learning-induced gene expression in the heads of two Nasonia species that differ in long-term memory formation
title_full_unstemmed Learning-induced gene expression in the heads of two Nasonia species that differ in long-term memory formation
title_short Learning-induced gene expression in the heads of two Nasonia species that differ in long-term memory formation
title_sort learning-induced gene expression in the heads of two nasonia species that differ in long-term memory formation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4440501/
https://www.ncbi.nlm.nih.gov/pubmed/25888126
http://dx.doi.org/10.1186/s12864-015-1355-1
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