{"title":"Geomagnetic intensity variation and deprivation elicit distinct transcriptomic responses in a migratory insect.","authors":"Wenhao Xie, Yuan Wang, Liangfeng Zou, Hui Qiu, Pin Li, Viacheslav Krylov, Yuanyuan Li, Weidong Pan, Fajun Chen, Guijun Wan","doi":"10.1111/imb.70066","DOIUrl":null,"url":null,"abstract":"<p><p>Geomagnetic field intensity varies along migratory routes; however, whether migratory insects respond similarly to intensity shifts and geomagnetic deprivation remains unclear. We compared transcriptomes of brown planthoppers, Nilaparvata lugens (Stål), reared under ~45 μT or ~50 μT fields, approximating intensities along their migratory route, or under a near-zero magnetic field (NZMF). The natural-range ~5 μT comparison identified 244 DEGs and a restricted functional response. 'Lipid transporter activity' was the only Gene Ontology term significant after false-discovery-rate correction, whereas 'response to light stimulus' and 'flavin adenine dinucleotide binding', both containing cryptochrome1 (Cry1), were nominally enriched. By contrast, NZMF identified 2753-3258 DEGs and enrichment of central carbon and amino-acid metabolism, peroxisomal function, redox regulation and clock-related genes. RT-qPCR validated representative genes. Given its differential expression under ecologically relevant geomagnetic intensity variation, established photoreceptive and circadian functions and previous NZMF responsiveness, Cry1 was examined by RNA interference as a step toward an eclosion-based magnetic response assay. Cry1 knockdown disrupted the diel eclosion rhythm, demonstrating its importance for eclosion timing and limiting this phenotype as a magnetic field intensity readout after knockdown. Together, natural-range geomagnetic variation and NZMF exposure may evoke qualitatively distinct magnetobiological response states rather than quantitatively different magnetic environments.</p>","PeriodicalId":13526,"journal":{"name":"Insect Molecular Biology","volume":" ","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2026-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Molecular Biology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/imb.70066","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Geomagnetic field intensity varies along migratory routes; however, whether migratory insects respond similarly to intensity shifts and geomagnetic deprivation remains unclear. We compared transcriptomes of brown planthoppers, Nilaparvata lugens (Stål), reared under ~45 μT or ~50 μT fields, approximating intensities along their migratory route, or under a near-zero magnetic field (NZMF). The natural-range ~5 μT comparison identified 244 DEGs and a restricted functional response. 'Lipid transporter activity' was the only Gene Ontology term significant after false-discovery-rate correction, whereas 'response to light stimulus' and 'flavin adenine dinucleotide binding', both containing cryptochrome1 (Cry1), were nominally enriched. By contrast, NZMF identified 2753-3258 DEGs and enrichment of central carbon and amino-acid metabolism, peroxisomal function, redox regulation and clock-related genes. RT-qPCR validated representative genes. Given its differential expression under ecologically relevant geomagnetic intensity variation, established photoreceptive and circadian functions and previous NZMF responsiveness, Cry1 was examined by RNA interference as a step toward an eclosion-based magnetic response assay. Cry1 knockdown disrupted the diel eclosion rhythm, demonstrating its importance for eclosion timing and limiting this phenotype as a magnetic field intensity readout after knockdown. Together, natural-range geomagnetic variation and NZMF exposure may evoke qualitatively distinct magnetobiological response states rather than quantitatively different magnetic environments.
期刊介绍:
Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins.
This includes research related to:
• insect gene structure
• control of gene expression
• localisation and function/activity of proteins
• interactions of proteins and ligands/substrates
• effect of mutations on gene/protein function
• evolution of insect genes/genomes, especially where principles relevant to insects in general are established
• molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations
• gene mapping using molecular tools
• molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects
Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).