Abstract
BackgroundCellular 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.ResultsRNA 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.ConclusionThis 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 materialThe online version of this article (doi:10.1186/s12864-015-1355-1) contains supplementary material, which is available to authorized users.
Highlights
Cellular processes underlying memory formation are evolutionary conserved, but natural variation in memory dynamics between animal species or populations is common
We have studied the genetic basis of variation in long-term memory (LTM) formation in the parasitic wasp Nasonia vitripennis and its closely related species N. giraulti
This study investigates differences in gene expression patterns related to LTM formation between the two Nasonia species, as a second approach to identify genes that are involved in the difference in LTM formation
Summary
Cellular processes underlying memory formation are evolutionary conserved, but natural variation in memory dynamics between animal species or populations is common. The ability to learn and form memory and the underlying cellular processes are evolutionary conserved, but there is substantial natural variation in memory dynamics between species [1,2]. Many animal species require multiple conditioning trials, which are spaced in time, to induce LTM consolidation. Such repeated learning experiences allow animals to evaluate the information before investing in costly LTM [5]. Ecological factors, including the value of the appetitive or aversive stimulus and the reliability of the learned association, are considered decisive for the number of trials required to form LTM [12]. Very little is currently known about genetic and neural factors that are involved in natural variation in LTM formation
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.