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dc.contributor.authorZimmer, C
dc.contributor.authorGarrood, W
dc.contributor.authorSingh, KS
dc.contributor.authorRandall, E
dc.contributor.authorLueke, B
dc.contributor.authorGutbrod, O
dc.contributor.authorMatthiesen, S
dc.contributor.authorKohler, M
dc.contributor.authorNauen, R
dc.contributor.authorDavies, TGE
dc.contributor.authorBass, C
dc.date.accessioned2018-01-25T11:13:53Z
dc.date.issued2018-01-11
dc.description.abstractGene duplication is a major source of genetic variation that has been shown to underpin the evolution of a wide range of adaptive traits [1, 2]. For example, duplication or amplification of genes encoding detoxification enzymes has been shown to play an important role in the evolution of insecticide resistance [3–5]. In this context, gene duplication performs an adaptive function as a result of its effects on gene dosage and not as a source of functional novelty [3, 6–8]. Here, we show that duplication and neofunctionalization of a cytochrome P450, CYP6ER1, led to the evolution of insecticide resistance in the brown planthopper. Considerable genetic variation was observed in the coding sequence of CYP6ER1 in populations of brown planthopper collected from across Asia, but just two sequence variants are highly overexpressed in resistant strains and metabolize imidacloprid. Both variants are characterized by profound amino-acid alterations in substrate recognition sites, and the introduction of these mutations into a susceptible P450 sequence is sufficient to confer resistance. CYP6ER1 is duplicated in resistant strains with individuals carrying paralogs with and without the gain-of-function mutations. Despite numerical parity in the genome, the susceptible and mutant copies exhibit marked asymmetry in their expression with the resistant paralogs overexpressed. In the primary resistance-conferring CYP6ER1 variant, this results from an extended region of novel sequence upstream of the gene that provides enhanced expression. Our findings illustrate the versatility of gene duplication in providing opportunities for functional and regulatory innovation during the evolution of an adaptive trait.en_GB
dc.description.sponsorshipThis project has received funding from the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation programme (grant agreement n°646625), the Biotechnology and Biological Sciences Research Council of the UK (BB/G023352/1), and Bayer Crop Science.en_GB
dc.identifier.citationVol. 28en_GB
dc.identifier.doi10.1016/j.cub.2017.11.060
dc.identifier.urihttp://hdl.handle.net/10871/31181
dc.language.isoenen_GB
dc.publisherElsevier (Cell Press)en_GB
dc.relation.sourceThe sequences reported in this paper have been deposited in the GenBank database (accession numbers GenBank: MF970458, GenBank: MF970459, GenBank: MF970460, GenBank: MF970461, GenBank: MF970462, and GenBank: MF970463).en_GB
dc.rights© 2017 The Authors. Published by Elsevier Ltd. Open Access funded by Biotechnology and Biological Sciences Research Council. Under a Creative Commons license: https://creativecommons.org/licenses/by/4.0/en_GB
dc.subjectresistanceen_GB
dc.subjectNilaparvata lugensen_GB
dc.subjectduplicationen_GB
dc.subjectneofunctionalizationen_GB
dc.subjectimidaclopriden_GB
dc.subjectP450en_GB
dc.titleNeofunctionalization of Duplicated P450 Genes Drives the Evolution of Insecticide Resistance in the Brown Planthopperen_GB
dc.typeArticleen_GB
dc.date.available2018-01-25T11:13:53Z
dc.identifier.issn0960-9822
dc.descriptionThis is the final version of the article. Available from Elsevier via the DOI in this record.en_GB
dc.identifier.journalCurrent Biologyen_GB


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