{"title":"Identification and sex-biased expression analysis of olfactory-related genes in Lymantria dispar based on transcriptome and qRT-PCR","authors":"Lina Yang , Dun Jiang , Weichao Ma , Shanchun Yan","doi":"10.1016/j.cbd.2025.101634","DOIUrl":null,"url":null,"abstract":"<div><div><em>Lymantria dispar</em>, a destructive forest pest, poses a significant threat to forest ecosystems. Olfaction plays a pivotal role in mate finding, host location, and oviposition site selection in insects. This study aimed to systematically characterize olfactory-related genes in adult <em>L. dispar</em> and examine sex-specific expression profiles, shedding light on the molecular mechanisms of olfactory perception in this species. Antennal transcriptomes of male and female <em>L. dispar</em> were sequenced, generating 36.61 Gb of high-quality clean data. A total of 134 olfactory-related genes were identified, including 40 odorant receptors (ORs), 12 gustatory receptors (GRs), 20 ionotropic receptors (IRs), 17 chemosensory proteins (CSPs), 38 odorant-binding proteins (OBPs), 3 odorant-degrading enzymes (ODEs), and 4 sensory neuron membrane proteins (SNMPs). Relative expression levels of these genes were validated by qRT-PCR, revealing that 28 genes were significantly upregulated in female antennae, while 32 genes exhibited higher expression in males. These findings aligned closely with the transcriptome data. This study provides a comprehensive characterization of olfactory-related genes in <em>L. dispar</em> antennae and uncovers their sex-biased expression, offering valuable insights into the molecular mechanisms of pheromone detection and other olfactory-driven behaviors in this pest species.</div></div>","PeriodicalId":55235,"journal":{"name":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","volume":"56 ","pages":"Article 101634"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology D-Genomics & Proteomics","FirstCategoryId":"99","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1744117X25002230","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Lymantria dispar, a destructive forest pest, poses a significant threat to forest ecosystems. Olfaction plays a pivotal role in mate finding, host location, and oviposition site selection in insects. This study aimed to systematically characterize olfactory-related genes in adult L. dispar and examine sex-specific expression profiles, shedding light on the molecular mechanisms of olfactory perception in this species. Antennal transcriptomes of male and female L. dispar were sequenced, generating 36.61 Gb of high-quality clean data. A total of 134 olfactory-related genes were identified, including 40 odorant receptors (ORs), 12 gustatory receptors (GRs), 20 ionotropic receptors (IRs), 17 chemosensory proteins (CSPs), 38 odorant-binding proteins (OBPs), 3 odorant-degrading enzymes (ODEs), and 4 sensory neuron membrane proteins (SNMPs). Relative expression levels of these genes were validated by qRT-PCR, revealing that 28 genes were significantly upregulated in female antennae, while 32 genes exhibited higher expression in males. These findings aligned closely with the transcriptome data. This study provides a comprehensive characterization of olfactory-related genes in L. dispar antennae and uncovers their sex-biased expression, offering valuable insights into the molecular mechanisms of pheromone detection and other olfactory-driven behaviors in this pest species.
期刊介绍:
Comparative Biochemistry & Physiology (CBP) publishes papers in comparative, environmental and evolutionary physiology.
Part D: Genomics and Proteomics (CBPD), focuses on “omics” approaches to physiology, including comparative and functional genomics, metagenomics, transcriptomics, proteomics, metabolomics, and lipidomics. Most studies employ “omics” and/or system biology to test specific hypotheses about molecular and biochemical mechanisms underlying physiological responses to the environment. We encourage papers that address fundamental questions in comparative physiology and biochemistry rather than studies with a focus that is purely technical, methodological or descriptive in nature.