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Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis

BACKGROUND: Selection acts on the phenotype, yet only the genotype is inherited. While both the phenotypic and genotypic response to short-term selection can be measured, the link between these is a major unsolved problem in evolutionary biology, in particular for complex behavioural phenotypes. RES...

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Autores principales: Kraaijeveld, Ken, Oostra, Vicencio, Liefting, Maartje, Wertheim, Bregje, de Meijer, Emile, Ellers, Jacintha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288879/
https://www.ncbi.nlm.nih.gov/pubmed/30526508
http://dx.doi.org/10.1186/s12864-018-5310-9
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author Kraaijeveld, Ken
Oostra, Vicencio
Liefting, Maartje
Wertheim, Bregje
de Meijer, Emile
Ellers, Jacintha
author_facet Kraaijeveld, Ken
Oostra, Vicencio
Liefting, Maartje
Wertheim, Bregje
de Meijer, Emile
Ellers, Jacintha
author_sort Kraaijeveld, Ken
collection PubMed
description BACKGROUND: Selection acts on the phenotype, yet only the genotype is inherited. While both the phenotypic and genotypic response to short-term selection can be measured, the link between these is a major unsolved problem in evolutionary biology, in particular for complex behavioural phenotypes. RESULTS: Here we characterize the genomic and the transcriptomic basis of associative learning ability in the parasitic wasp Nasonia vitripennis and use gene network analysis to link the two. We artificially selected for improved associative learning ability in four independent pairs of lines and identified signatures of selection across the genome. Allele frequency diverged consistently between the selected and control lines in 118 single nucleotide polymorphisms (SNPs), clustering in 51 distinct genomic regions containing 128 genes. The majority of SNPs were found in regulatory regions, suggesting a potential role for gene expression evolution. We therefore sequenced the transcriptomes of selected and control lines and identified 36 consistently differentially expressed transcripts with large changes in expression. None of the differentially expressed genes also showed sequence divergence as a result of selection. Instead, gene network analysis showed many of the genes with consistent allele frequency differences and all of the differentially expressed genes to cluster in a single co-expression network. At a functional level, both genomic and transcriptomic analyses implicated members of gene networks known to be involved in neural plasticity and cognitive processes. CONCLUSIONS: Taken together, our results reveal how specific cognitive abilities can readily respond to selection via a complex interplay between regulatory and sequence evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5310-9) contains supplementary material, which is available to authorized users.
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spelling pubmed-62888792018-12-14 Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis Kraaijeveld, Ken Oostra, Vicencio Liefting, Maartje Wertheim, Bregje de Meijer, Emile Ellers, Jacintha BMC Genomics Research Article BACKGROUND: Selection acts on the phenotype, yet only the genotype is inherited. While both the phenotypic and genotypic response to short-term selection can be measured, the link between these is a major unsolved problem in evolutionary biology, in particular for complex behavioural phenotypes. RESULTS: Here we characterize the genomic and the transcriptomic basis of associative learning ability in the parasitic wasp Nasonia vitripennis and use gene network analysis to link the two. We artificially selected for improved associative learning ability in four independent pairs of lines and identified signatures of selection across the genome. Allele frequency diverged consistently between the selected and control lines in 118 single nucleotide polymorphisms (SNPs), clustering in 51 distinct genomic regions containing 128 genes. The majority of SNPs were found in regulatory regions, suggesting a potential role for gene expression evolution. We therefore sequenced the transcriptomes of selected and control lines and identified 36 consistently differentially expressed transcripts with large changes in expression. None of the differentially expressed genes also showed sequence divergence as a result of selection. Instead, gene network analysis showed many of the genes with consistent allele frequency differences and all of the differentially expressed genes to cluster in a single co-expression network. At a functional level, both genomic and transcriptomic analyses implicated members of gene networks known to be involved in neural plasticity and cognitive processes. CONCLUSIONS: Taken together, our results reveal how specific cognitive abilities can readily respond to selection via a complex interplay between regulatory and sequence evolution. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12864-018-5310-9) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-10 /pmc/articles/PMC6288879/ /pubmed/30526508 http://dx.doi.org/10.1186/s12864-018-5310-9 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
Kraaijeveld, Ken
Oostra, Vicencio
Liefting, Maartje
Wertheim, Bregje
de Meijer, Emile
Ellers, Jacintha
Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis
title Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis
title_full Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis
title_fullStr Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis
title_full_unstemmed Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis
title_short Regulatory and sequence evolution in response to selection for improved associative learning ability in Nasonia vitripennis
title_sort regulatory and sequence evolution in response to selection for improved associative learning ability in nasonia vitripennis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6288879/
https://www.ncbi.nlm.nih.gov/pubmed/30526508
http://dx.doi.org/10.1186/s12864-018-5310-9
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