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dc.contributor.authorDoyle, T
dc.contributor.authorJimenez-Guri, E
dc.contributor.authorHawkes, WLS
dc.contributor.authorMassy, R
dc.contributor.authorMantica, F
dc.contributor.authorPermanyer, J
dc.contributor.authorCozzuto, L
dc.contributor.authorHermoso Pulido, T
dc.contributor.authorBaril, T
dc.contributor.authorHayward, A
dc.contributor.authorIrimia, M
dc.contributor.authorChapman, JW
dc.contributor.authorBass, C
dc.contributor.authorWotton, KR
dc.date.accessioned2022-07-26T12:33:51Z
dc.date.issued2022-07-08
dc.date.updated2022-07-26T10:41:37Z
dc.description.abstractInsects are capable of extraordinary feats of long-distance movement that have profound impacts on the function of terrestrial ecosystems. The ability to undertake these movements arose multiple times through the evolution of a suite of traits that make up the migratory syndrome, however the underlying genetic pathways involved remain poorly understood. Migratory hoverflies (Diptera: Syrphidae) are an emerging model group for studies of migration. They undertake seasonal movements in huge numbers across large parts of the globe and are important pollinators, biological control agents and decomposers. Here, we assembled a high-quality draft genome of the marmalade hoverfly (Episyrphus balteatus). We leveraged this genomic resource to undertake a genome-wide transcriptomic comparison of actively migrating Episyrphus, captured from a high mountain pass as they flew south to overwinter, with the transcriptomes of summer forms which were non-migratory. We identified 1543 genes with very strong evidence for differential expression. Interrogation of this gene set reveals a remarkable range of roles in metabolism, muscle structure and function, hormonal regulation, immunity, stress resistance, flight and feeding behaviour, longevity, reproductive diapause and sensory perception. These features of the migrant phenotype have arisen by the integration and modification of pathways such as insulin signalling for diapause and longevity, JAK/SAT for immunity, and those leading to octopamine production and fuelling to boost flight capabilities. Our results provide a powerful genomic resource for future research, and paint a comprehensive picture of global expression changes in an actively migrating insect, identifying key genomic components involved in this important life-history strategy.en_GB
dc.description.sponsorshipRoyal Societyen_GB
dc.description.sponsorshipNatural Environment Research Council (NERC)en_GB
dc.description.sponsorshipBiotechnology and Biological Sciences Research Council (BBSRC)en_GB
dc.format.mediumPrint-Electronic
dc.identifier.citationPublished online 8 July 2022en_GB
dc.identifier.doihttps://doi.org/10.1111/mec.16588
dc.identifier.grantnumberUF150126en_GB
dc.identifier.grantnumberRGF\EA\180083en_GB
dc.identifier.grantnumberRGF\R1\180047en_GB
dc.identifier.grantnumberBB/M009122/1en_GB
dc.identifier.grantnumberBB/N020146/1en_GB
dc.identifier.urihttp://hdl.handle.net/10871/130389
dc.identifierORCID: 0000-0003-3957-3765 (Doyle, Toby)
dc.identifierORCID: 0000-0002-5936-7531 (Baril, Tobias)
dc.identifierORCID: 0000-0002-7475-4441 (Chapman, Jason W)
dc.identifierORCID: 0000-0002-8672-9948 (Wotton, Karl R)
dc.language.isoenen_GB
dc.publisherWileyen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/35801824en_GB
dc.relation.urlhttps://doi.org/10.6084/m9.figshare.19333181en_GB
dc.rights© 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.en_GB
dc.subjectdifferential gene expressionen_GB
dc.subjectgenetics of migrationen_GB
dc.subjectinsect migrationen_GB
dc.subjectmigratory hoverfliesen_GB
dc.subjectmolecular adaptationsen_GB
dc.subjectsyrphidaeen_GB
dc.titleGenome-wide transcriptomic changes reveal the genetic pathways involved in insect migrationen_GB
dc.typeArticleen_GB
dc.date.available2022-07-26T12:33:51Z
dc.identifier.issn0962-1083
exeter.place-of-publicationEngland
dc.descriptionThis is the final version. Available on open access from Wiley via the DOI in this recorden_GB
dc.descriptionData availability statement: The datasets and metadata supporting the results of this article have been deposited at DDBJ/ENA/GenBank and are available via Bioproject PRJNA720810. The genome assembly described in this paper has been deposited under the accession JAGTYB000000000. The version described in this paper is version JAGTYB010000000. Tissue level RNAseq data is available from the Gene Expression Omnibus (GEO) repository via GSE205498. Genome and repeat annotation files are available on figshare 10.6084/m9.figshare.19333181.en_GB
dc.identifier.eissn1365-294X
dc.identifier.journalMolecular Ecologyen_GB
dc.relation.ispartofMol Ecol
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2022-06-27
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2022-07-08
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-07-26T12:31:21Z
refterms.versionFCDVoR
refterms.dateFOA2022-07-26T12:33:52Z
refterms.panelAen_GB
refterms.dateFirstOnline2022-07-08


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© 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's licence is described as © 2022 The Authors. Molecular Ecology published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.