Polygenic response to selection by transgenic Bt-expressing crops in wild Helicoverpa zea and characterization of a major effect locus

Abstract Strong and shifting selective pressures of the Anthropocene are rapidly shaping phenomes and genomes of organisms worldwide. Crops expressing pesticidal proteins from Bacillus thuringiensis (Bt) represent one major selective force on insect genomes. Here we characterize a rapid response to...

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Main Authors: Katherine L. Taylor, Jane Quackenbush, Cara Lamberty, Kelly A. Hamby, Megan L. Fritz
Format: Article
Language:English
Published: BMC 2024-12-01
Series:BMC Genomics
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Online Access:https://doi.org/10.1186/s12864-024-11160-x
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author Katherine L. Taylor
Jane Quackenbush
Cara Lamberty
Kelly A. Hamby
Megan L. Fritz
author_facet Katherine L. Taylor
Jane Quackenbush
Cara Lamberty
Kelly A. Hamby
Megan L. Fritz
author_sort Katherine L. Taylor
collection DOAJ
description Abstract Strong and shifting selective pressures of the Anthropocene are rapidly shaping phenomes and genomes of organisms worldwide. Crops expressing pesticidal proteins from Bacillus thuringiensis (Bt) represent one major selective force on insect genomes. Here we characterize a rapid response to selection by Bt crops in a major crop pest, Helicoverpa zea. We reveal the polygenic architecture of Bt resistance evolution in H. zea and identify multiple genomic regions underlying this trait. In the genomic region of largest effect, we identified a gene amplification event, where resistant individuals showed variation in copy number for multiple genes. Signals of this amplification increased over time, consistent with the history of field-evolved Bt resistance evolution. Modern wild populations from disparate geographical regions are positive for this variant at high, but not fixed, allele frequencies. We also detected selection against single copy variants at this locus in wild H. zea collected from Bt expressing plants, further supporting its role in resistance. Multiple genes were annotated in this genomic region, and all appeared to be significantly upregulated in Bt resistant H. zea. We functionally characterized genes within the copy number variant (CNV), providing insight into their potential roles in resistance evolution. Our findings reveal the nature of rapid genome evolution in a major crop pest following anthropogenic selection and highlight the role that CNVs can have in rapid evolutionary responses.
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spelling doaj-art-a56e4cd664da4a3d875069e475d059082024-12-29T12:11:03ZengBMCBMC Genomics1471-21642024-12-0125111710.1186/s12864-024-11160-xPolygenic response to selection by transgenic Bt-expressing crops in wild Helicoverpa zea and characterization of a major effect locusKatherine L. Taylor0Jane Quackenbush1Cara Lamberty2Kelly A. Hamby3Megan L. Fritz4Department of Entomology, University of MarylandDepartment of Entomology, University of MarylandDepartment of Entomology, University of MarylandDepartment of Entomology, University of MarylandDepartment of Entomology, University of MarylandAbstract Strong and shifting selective pressures of the Anthropocene are rapidly shaping phenomes and genomes of organisms worldwide. Crops expressing pesticidal proteins from Bacillus thuringiensis (Bt) represent one major selective force on insect genomes. Here we characterize a rapid response to selection by Bt crops in a major crop pest, Helicoverpa zea. We reveal the polygenic architecture of Bt resistance evolution in H. zea and identify multiple genomic regions underlying this trait. In the genomic region of largest effect, we identified a gene amplification event, where resistant individuals showed variation in copy number for multiple genes. Signals of this amplification increased over time, consistent with the history of field-evolved Bt resistance evolution. Modern wild populations from disparate geographical regions are positive for this variant at high, but not fixed, allele frequencies. We also detected selection against single copy variants at this locus in wild H. zea collected from Bt expressing plants, further supporting its role in resistance. Multiple genes were annotated in this genomic region, and all appeared to be significantly upregulated in Bt resistant H. zea. We functionally characterized genes within the copy number variant (CNV), providing insight into their potential roles in resistance evolution. Our findings reveal the nature of rapid genome evolution in a major crop pest following anthropogenic selection and highlight the role that CNVs can have in rapid evolutionary responses.https://doi.org/10.1186/s12864-024-11160-xHelicoverpa zeaBacillus thuringiensisCry toxinResistance evolutionGene amplificationStructural variant
spellingShingle Katherine L. Taylor
Jane Quackenbush
Cara Lamberty
Kelly A. Hamby
Megan L. Fritz
Polygenic response to selection by transgenic Bt-expressing crops in wild Helicoverpa zea and characterization of a major effect locus
BMC Genomics
Helicoverpa zea
Bacillus thuringiensis
Cry toxin
Resistance evolution
Gene amplification
Structural variant
title Polygenic response to selection by transgenic Bt-expressing crops in wild Helicoverpa zea and characterization of a major effect locus
title_full Polygenic response to selection by transgenic Bt-expressing crops in wild Helicoverpa zea and characterization of a major effect locus
title_fullStr Polygenic response to selection by transgenic Bt-expressing crops in wild Helicoverpa zea and characterization of a major effect locus
title_full_unstemmed Polygenic response to selection by transgenic Bt-expressing crops in wild Helicoverpa zea and characterization of a major effect locus
title_short Polygenic response to selection by transgenic Bt-expressing crops in wild Helicoverpa zea and characterization of a major effect locus
title_sort polygenic response to selection by transgenic bt expressing crops in wild helicoverpa zea and characterization of a major effect locus
topic Helicoverpa zea
Bacillus thuringiensis
Cry toxin
Resistance evolution
Gene amplification
Structural variant
url https://doi.org/10.1186/s12864-024-11160-x
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