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Multiple origins of a single point mutation in the cotton bollworm tetraspanin gene confers dominant resistance to Bt cotton

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/ps.5541openalex-snapshot
Bt resistance alleles in field populations of pink bollworm from China: Similarities with the United States and decreased frequency from 2012 to 2015
inferredcites →https://doi.org/10.1007/pl00006504openalex-snapshot
Multiple Origins of Cyclodiene Insecticide Resistance in Tribolium castaneum (Coleoptera: Tenebrionidae)
inferredcites →https://doi.org/10.1016/j.cois.2016.04.002openalex-snapshot
Bt resistance in Australian insect pest species
inferredcites →https://doi.org/10.1016/j.ibmb.2004.08.003openalex-snapshot
DNA-based detection of Bt resistance alleles in pink bollworm
inferredcites →https://doi.org/10.1016/j.ibmb.2004.12.004openalex-snapshot
Evidence for multiple origins of identical insecticide resistance mutations in the aphid Myzus persicae
inferredcites →https://doi.org/10.1016/j.ibmb.2005.10.007openalex-snapshot
Multiple origins of pyrethroid resistance in sympatric biotypes of Bemisia tabaci (Hemiptera: Aleyrodidae)
inferredcites →https://doi.org/10.1016/j.ibmb.2014.02.006openalex-snapshot
Global distribution and origin of target site insecticide resistance mutations in Tetranychus urticae
inferredcites →https://doi.org/10.1016/j.jip.2007.03.008openalex-snapshot
The diversity of Bt resistance genes in species of Lepidoptera
inferredcites →https://doi.org/10.1016/j.pestbp.2012.08.001openalex-snapshot
Multiple evolutionary origins of knockdown resistance (kdr) in pyrethroid-resistant Colorado potato beetle, Leptinotarsa decemlineata
inferredcites →https://doi.org/10.1016/j.pestbp.2013.06.007openalex-snapshot
DNA-based screening for an intracellular cadherin mutation conferring non-recessive Cry1Ac resistance in field populations of Helicoverpa armigera
inferredcites →https://doi.org/10.1016/j.tibtech.2015.12.011openalex-snapshot
Can Pyramids and Seed Mixtures Delay Resistance to Bt Crops?
inferredcites →https://doi.org/10.1016/j.tig.2004.01.003openalex-snapshot
The genetics and genomics of insecticide resistance
inferredcites →https://doi.org/10.1017/s0007485308006226openalex-snapshot
Introgression of a disrupted cadherin gene enables susceptibleHelicoverpa armigerato obtain resistance toBacillus thuringiensistoxin Cry1Ac
inferredcites →https://doi.org/10.1038/350151a0openalex-snapshot
Worldwide migration of amplified insecticide resistance genes in mosquitoes
inferredcites →https://doi.org/10.1038/nature11153openalex-snapshot
Widespread adoption of Bt cotton and insecticide decrease promotes biocontrol services
inferredcites →https://doi.org/10.1038/nbt.2597openalex-snapshot
Insect resistance to Bt crops: lessons from the first billion acres
inferredcites →https://doi.org/10.1038/nbt.3100openalex-snapshot
Large-scale test of the natural refuge strategy for delaying insect resistance to transgenic Bt crops
inferredcites →https://doi.org/10.1038/nbt.3974openalex-snapshot
Surge in insect resistance to transgenic crops and prospects for sustainability
inferredcites →https://doi.org/10.1038/nbt1382openalex-snapshot
Insect resistance to Bt crops: evidence versus theory
inferredcites →https://doi.org/10.1038/nmeth.4285openalex-snapshot
ModelFinder: fast model selection for accurate phylogenetic estimates
inferredcites →https://doi.org/10.1038/srep09807openalex-snapshot
A seed mixture increases dominance of resistance to Bt cotton in Helicoverpa zea
inferredcites →https://doi.org/10.1046/j.1466-7657.2002.00139.x-i1openalex-snapshot
Detection and monitoring of insect resistance to transgenic Bt crops
inferredcites →https://doi.org/10.1073/pnas.1200156109openalex-snapshot
Diverse genetic basis of field-evolved resistance to Bt cotton in cotton bollworm from China
inferredcites →https://doi.org/10.1073/pnas.1203647109openalex-snapshot
Economic impacts and impact dynamics of Bt ( Bacillus thuringiensis ) cotton in India
inferredcites →https://doi.org/10.1073/pnas.1700396114openalex-snapshot
Hybridizing transgenic Bt cotton with non-Bt cotton counters resistance in pink bollworm
inferredcites →https://doi.org/10.1073/pnas.1812138115openalex-snapshot
Dominant point mutation in a tetraspanin gene associated with field-evolved resistance of cotton bollworm to transgenic Bt cotton
inferredcites →https://doi.org/10.1073/pnas.94.24.12780openalex-snapshot
Global variation in the genetic and biochemical basis of diamondback moth resistance to Bacillus thuringiensis
inferredcites →https://doi.org/10.1093/bioinformatics/btr507openalex-snapshot
FLASH: fast length adjustment of short reads to improve genome assemblies
inferredcites →https://doi.org/10.1093/bioinformatics/btu170openalex-snapshot
Trimmomatic: a flexible trimmer for Illumina sequence data
inferredcites →https://doi.org/10.1093/molbev/msu300openalex-snapshot
IQ-TREE: A Fast and Effective Stochastic Algorithm for Estimating Maximum-Likelihood Phylogenies
inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot
MUSCLE: multiple sequence alignment with high accuracy and high throughput
inferredcites →https://doi.org/10.1098/rstb.1998.0322openalex-snapshot
An overview of the evolution of overproduced esterases in the mosquito Culex pipiens
inferredcites →https://doi.org/10.1111/brv.12440openalex-snapshot
The evolutionary origins of pesticide resistance
inferredcites →https://doi.org/10.1111/eva.12099openalex-snapshot
Dominant resistance to B t cotton and minor cross‐resistance to B t toxin C ry2Ab in cotton bollworm from C hina
inferredcites →https://doi.org/10.1111/j.1420-9101.2004.00695.xopenalex-snapshot
Delaying evolution of insect resistance to transgenic crops by decreasing dominance and heritability
inferredcites →https://doi.org/10.1111/j.1574-6941.2006.00060.xopenalex-snapshot
Comparison of prokaryotic diversity at offshore oceanic locations reveals a different microbiota in the Mediterranean Sea
inferredcites →https://doi.org/10.1111/j.1574-6976.2012.00341.xopenalex-snapshot
Bacillus thuringiensis insecticidal three-domain Cry toxins: mode of action, insect resistance and consequences for crop protection
inferredcites →https://doi.org/10.1111/j.1744-7917.2006.00070.xopenalex-snapshot
Author Guidelines
inferredcites →https://doi.org/10.1111/mec.13197openalex-snapshot
Contemporary evolution of resistance at the major insecticide target site gene Ace‐1 by mutation and copy number variation in the malaria mosquito Anopheles gambiae
inferredcites →https://doi.org/10.1126/science.1067226openalex-snapshot
Plant Biotechnology in China
inferredcites →https://doi.org/10.1126/science.1074170openalex-snapshot
A Single P450 Allele Associated with Insecticide Resistance in Drosophila
inferredcites →https://doi.org/10.1126/science.1160550openalex-snapshot
Suppression of Cotton Bollworm in Multiple Crops in China in Areas with Bt Toxin–Containing Cotton
inferredcites →https://doi.org/10.1126/science.aar3780openalex-snapshot
Wicked evolution: Can we address the sociobiological dilemma of pesticide resistance?
inferredcites →https://doi.org/10.1146/annurev.ento.43.1.701openalex-snapshot
Sustainability of Transgenic Insecticidal Cultivars: Integrating Pest Genetics and Ecology
inferredcites →https://doi.org/10.1186/s12915-017-0402-6openalex-snapshot
Genomic innovations, transcriptional plasticity and gene loss underlying the evolution and divergence of two highly polyphagous and invasive Helicoverpa pest species
inferredcites →https://doi.org/10.1371/journal.pone.0001243openalex-snapshot
Multiple Origins of Knockdown Resistance Mutations in the Afrotropical Mosquito Vector Anopheles gambiae
inferredcites →https://doi.org/10.1371/journal.pone.0022874openalex-snapshot
Early Warning of Cotton Bollworm Resistance Associated with Intensive Planting of Bt Cotton in China
inferredcites →https://doi.org/10.1371/journal.pone.0043543openalex-snapshot
Multiple Origins of the Sodium Channel kdr Mutations in Codling Moth Populations
inferredcites →https://doi.org/10.1371/journal.pone.0069675openalex-snapshot
Dominant Inheritance of Field-Evolved Resistance to Bt Corn in Busseola fusca
inferredcites →https://doi.org/10.1603/0022-0493-95.4.832openalex-snapshot
Evaluation of the Natural Refuge Function for Helicoverpa armigera (Lepidoptera: Noctuidae) within Bacillus thuringiensis Transgenic Cotton Growing Areas in North China
inferredcites →https://doi.org/10.4161/gmcr.20194openalex-snapshot
Successes and challenges of managing resistance in Helicoverpa armigera to Bt cotton in Australia
inferredcites →https://doi.org/10.6084/m9.figshare.963153.v1openalex-snapshot
Aligning sequence reads, clone sequences and assembly con*gs with BWA-MEM

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4679338openalex-extracted
Frequencies of Insecticide Resistance Mutations Detected by the Amplicon Sequencing in Plutella Xylostella and Spodoptera Exigua from China
inferred← citeshttps://doi.org/10.1002/ps.6327openalex-snapshot
Amplicon sequencing detects mutations associated with pyrethroid resistance in Bemisia tabaci (Hemiptera: Aleyrodidae)
inferred← citeshttps://doi.org/10.1002/ps.6776openalex-snapshot
A feasibility trial of genomics‐based diagnosis detecting insecticide resistance of the diamondback moth
inferred← citeshttps://doi.org/10.1002/ps.7845openalex-snapshot
Improved effects of Helicoverpa armigera nucleopolyhedrovirus integrated with Campoletis chlorideae against H. armigera and impact of the virus on the parasitoid
inferred← citeshttps://doi.org/10.1002/ps.8561openalex-snapshot
Monitoring acaricide resistance and the frequency of associated target‐site mutations in Tetranychus urticae populations from rose glasshouses in China
inferred← citeshttps://doi.org/10.1002/ps.8803openalex-snapshot
Population genomics reveals population structure and local adaptation of the Helicoverpa armigera lineage in Xinjiang, China
inferred← citeshttps://doi.org/10.1002/ps.8845openalex-snapshot
Genetic mutations and insecticide resistance in Diaphorina citri: a comparative study across Chinese citrus regions
inferred← citeshttps://doi.org/10.1016/bs.aiip.2023.09.005openalex-snapshot
Mechanisms and molecular genetics of insect resistance to insecticidal proteins from Bacillus thuringiensis
inferred← citeshttps://doi.org/10.1016/j.isci.2023.106768openalex-snapshot
Refuges of conventional host plants counter dominant resistance of cotton bollworm to transgenic Bt cotton
inferred← citeshttps://doi.org/10.1016/j.jia.2024.09.022openalex-snapshot
Species-specific evolution of lepidopteran TspC5 tetraspanins associated with dominant resistance to Bacillus thuringiensis toxin Cry1Ac
inferred← citeshttps://doi.org/10.1016/j.pestbp.2023.105542openalex-snapshot
Absence of known knockdown resistance mutations but fixation of CYP337B3 was detected in field populations of Helicoverpa armigera across China
inferred← citeshttps://doi.org/10.1016/j.pestbp.2025.106929openalex-snapshot
Ongoing insecticide resistance evolution in beet armyworm via changes in the utilization of pre-existing and new mutations
inferred← citeshttps://doi.org/10.1016/j.pestbp.2026.107187openalex-snapshot
From midgut targets to genomic surveillance: Mechanism-informed diagnostics of resistance to Bt crops
inferred← citeshttps://doi.org/10.1016/j.plantsci.2024.112079openalex-snapshot
Cotton plants overexpressing the Bacillus thuringiensis Cry23Aa and Cry37Aa binary-like toxins exhibit high resistance to the cotton boll weevil (Anthonomus grandis)
inferred← citeshttps://doi.org/10.1038/s42003-025-08658-9openalex-snapshot
Population genomics reveal multiple independent origins of pesticide resistance in the polyphagous pest, Tetranychus urticae
inferred← citeshttps://doi.org/10.1080/21645698.2022.2025725openalex-snapshot
Comparison of genetically modified insect-resistant maize and non-transgenic maize revealed changes in soil metabolomes but not in rhizosphere bacterial community
inferred← citeshttps://doi.org/10.1093/jee/toac182openalex-snapshot
Population Genomics of Nonrecessive Resistance to Bt Toxin Cry1Ac in Helicoverpa armigera From Northern China
inferred← citeshttps://doi.org/10.1093/jee/toae268openalex-snapshot
Detection and functional validation of point mutations in acetylcholinesterase-1 associated with organophosphate resistance in field populations of Helicoverpa armigera
inferred← citeshttps://doi.org/10.1093/jisesa/iead059openalex-snapshot
Response patterns of lncRNAs of theSpodoptera frugiperda(Lepidoptera: Noctuidae) larvae under 23 pesticide treatments
inferred← citeshttps://doi.org/10.1111/1744-7917.13402openalex-snapshot
Genome‐wide identification and phylogenetic analysis of the tetraspanin gene family in lepidopteran insects and expression profiling analysis in Helicoverpa armigera
inferred← citeshttps://doi.org/10.1111/tpj.16536openalex-snapshot
Rice tetraspanins express in specific domains of diverse tissues and regulate plant architecture and root growth
inferred← citeshttps://doi.org/10.1146/annurev-ento-080421-071655openalex-snapshot
Determinants of Insecticide Resistance Evolution: Comparative Analysis Among Heliothines
inferred← citeshttps://doi.org/10.3389/fmicb.2021.670402openalex-snapshot
Evaluating Cross-Resistance to Cry and Vip Toxins in Four Strains of Helicoverpa armigera With Different Genetic Mechanisms of Resistance to Bt Toxin Cry1Ac
inferred← citeshttps://doi.org/10.7554/elife.106288openalex-snapshot
Recurrent mutations drive the rapid evolution of pesticide resistance in the two-spotted spider mite Tetranychus urticae
inferred← citeshttps://doi.org/10.7554/elife.106288.1openalex-snapshot
Unprecedented Number of Recurrent Mutations Drive the Rapid Evolution of Pesticide Resistance in a Notorious Pest
inferred← citeshttps://doi.org/10.7554/elife.106288.2openalex-snapshot
Recurrent Mutations Drive the Rapid Evolution of Pesticide Resistance in the Two-spotted Spider Mite Tetranychus urticae
inferred← citeshttps://doi.org/10.7554/elife.106288.3openalex-snapshot
Recurrent mutations drive the rapid evolution of pesticide resistance in the two-spotted spider mite Tetranychus urticae
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