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Insecticide resistance mediated 1 by an exon skipping event

Berger, Madeleine; Puinean, Alin M.; Randall, Emma; Zimmer, Christoph T.; Silva, Wellington M.; Bielza, Pablo; Field, Linda M.; Hughes, David; Mellor, Ian R.; Hassani-Pak, Keywan; Siqueira, Herbert A.A.; Williamson, Martin S.; Bass, Chris

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Authors

Madeleine Berger

Alin M. Puinean

Emma Randall

Christoph T. Zimmer

Wellington M. Silva

Pablo Bielza

Linda M. Field

David Hughes

Ian R. Mellor

Keywan Hassani-Pak

Herbert A.A. Siqueira

Martin S. Williamson

Chris Bass



Abstract

Many genes increase coding capacity by alternate exon usage. The gene encoding the insect nicotinic acetylcholine receptor (nAChR) a6 subunit, target of the bio-insecticide spinosad, is one example of this and expands protein diversity via alternative splicing of mutually exclusive exons. Here, we show that spinosad resistance in the tomato leaf miner, Tuta absoluta is associated with aberrant regulation of splicing of Taa6 resulting in a novel form of insecticide resistance mediated by exon skipping. Sequencing of the a6 subunit cDNA from spinosad selected and unselected strains of T. absoluta revealed all Taa6 transcripts of the selected strain were devoid of exon 3, with comparison of genomic DNA and mRNA revealing this is a result of exon skipping. Exon skipping cosegregated with spinosad resistance in survival bioassays, and functional characterization of this alteration using modified human nAChR a7, a model of insect a6, demonstrated that exon 3 is essential for receptor function and hence spinosad sensitivity. DNA and RNA sequencing analyses suggested that exon skipping did not result from genetic alterations in intronic or exonic cis-regulatory elements, but rather was associated with a single epigenetic modification downstream of exon 3a, and quantitative changes in the expression of trans-acting proteins that have known roles in the regulation of alternative splicing. Our results demonstrate that the intrinsic capacity of the a6 gene to generate transcript diversity via alternative splicing can be readily exploited during the evolution of resistance and identifies exon skipping as a molecular alteration conferring insecticide resistance.

Citation

Berger, M., Puinean, A. M., Randall, E., Zimmer, C. T., Silva, W. M., Bielza, P., …Bass, C. (2016). Insecticide resistance mediated 1 by an exon skipping event. Molecular Ecology, 25(22), https://doi.org/10.1111/mec.13882

Journal Article Type Article
Acceptance Date Oct 5, 2016
Publication Date Nov 2, 2016
Deposit Date Jan 25, 2017
Publicly Available Date Jan 25, 2017
Journal Molecular Ecology
Print ISSN 0962-1083
Electronic ISSN 1365-294X
Publisher Wiley
Peer Reviewed Peer Reviewed
Volume 25
Issue 22
DOI https://doi.org/10.1111/mec.13882
Keywords Alternative splicing, nicotinic acetylcholine receptor, spinosad, Tuta absoluta
Public URL https://nottingham-repository.worktribe.com/output/830344
Publisher URL http://onlinelibrary.wiley.com/doi/10.1111/mec.13882/full
Contract Date Jan 25, 2017

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