Jaqueline R Silva, Gabriel F Pelentir, Danilo T Amaral, Cassius Stevani, Vadim R Viviani
{"title":"发光和非发光的干酪蛉幼虫转录组学、蛋白质组学和生化比较(双翅目:干酪蛉科)。","authors":"Jaqueline R Silva, Gabriel F Pelentir, Danilo T Amaral, Cassius Stevani, Vadim R Viviani","doi":"10.1111/imb.70008","DOIUrl":null,"url":null,"abstract":"<p><p>Bioluminescence (BL) in the Keroplatinae subfamily (Diptera: Keroplatidae) is found in Keroplatus, Neoceroplatus and Orfelia fultoni larvae. In O. fultoni, BL involves an oligomeric luciferase, a luciferin called keroplatin, which is associated with a substrate binding fraction (SBF), whose molecular identity and function remain uncertain. Non-luminescent web-constructing predatory larvae of Neoditomyia sp. (Keroplatinae) also contain keroplatin and SBF in their bodies, suggesting additional unknown roles for this compound in this subfamily. To identify gene products differentially expressed between luminescent and non-luminescent larvae, especially those associated with luciferase, SBF and keroplatin synthesis, here we compared the transcriptional and proteomic profiles of Neoditomyia sp., O. fultoni and Arachnocampa larvae and conducted biochemical assays. Similarly to O. fultoni, Neoditomyia sp. displays an abundance of hexamerin isoforms and transcripts associated with the tryptophan and kynurenine pathway, which is potentially involved with keroplatin synthesis and silk production. Despite displaying a similar electrophoretic pattern of Orfelia luciferase purified fractions, no luciferase activity was detected in Neoditomyia purified fractions. The SBF-enriched fractions from O. fultoni and Neoditomyia revealed a similar abundance of hexamerins, the presence of flavin-dependent reductases, keroplatin and riboflavin. The results indicate that the SBF consists of protein aggregates associated with riboflavin and keroplatin, which is used as luciferin in bioluminescent species and for other still unveiled physiological functions in non-luminescent species.</p>","PeriodicalId":13526,"journal":{"name":"Insect Molecular Biology","volume":" ","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2025-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Transcriptomic, proteomic and biochemical comparison of luminescent and non-luminescent Keroplatinae larvae (Diptera: Keroplatidae).\",\"authors\":\"Jaqueline R Silva, Gabriel F Pelentir, Danilo T Amaral, Cassius Stevani, Vadim R Viviani\",\"doi\":\"10.1111/imb.70008\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bioluminescence (BL) in the Keroplatinae subfamily (Diptera: Keroplatidae) is found in Keroplatus, Neoceroplatus and Orfelia fultoni larvae. In O. fultoni, BL involves an oligomeric luciferase, a luciferin called keroplatin, which is associated with a substrate binding fraction (SBF), whose molecular identity and function remain uncertain. Non-luminescent web-constructing predatory larvae of Neoditomyia sp. (Keroplatinae) also contain keroplatin and SBF in their bodies, suggesting additional unknown roles for this compound in this subfamily. To identify gene products differentially expressed between luminescent and non-luminescent larvae, especially those associated with luciferase, SBF and keroplatin synthesis, here we compared the transcriptional and proteomic profiles of Neoditomyia sp., O. fultoni and Arachnocampa larvae and conducted biochemical assays. Similarly to O. fultoni, Neoditomyia sp. displays an abundance of hexamerin isoforms and transcripts associated with the tryptophan and kynurenine pathway, which is potentially involved with keroplatin synthesis and silk production. Despite displaying a similar electrophoretic pattern of Orfelia luciferase purified fractions, no luciferase activity was detected in Neoditomyia purified fractions. The SBF-enriched fractions from O. fultoni and Neoditomyia revealed a similar abundance of hexamerins, the presence of flavin-dependent reductases, keroplatin and riboflavin. The results indicate that the SBF consists of protein aggregates associated with riboflavin and keroplatin, which is used as luciferin in bioluminescent species and for other still unveiled physiological functions in non-luminescent species.</p>\",\"PeriodicalId\":13526,\"journal\":{\"name\":\"Insect Molecular Biology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-08-21\",\"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.70008\",\"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}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Molecular Biology","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/imb.70008","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}
Transcriptomic, proteomic and biochemical comparison of luminescent and non-luminescent Keroplatinae larvae (Diptera: Keroplatidae).
Bioluminescence (BL) in the Keroplatinae subfamily (Diptera: Keroplatidae) is found in Keroplatus, Neoceroplatus and Orfelia fultoni larvae. In O. fultoni, BL involves an oligomeric luciferase, a luciferin called keroplatin, which is associated with a substrate binding fraction (SBF), whose molecular identity and function remain uncertain. Non-luminescent web-constructing predatory larvae of Neoditomyia sp. (Keroplatinae) also contain keroplatin and SBF in their bodies, suggesting additional unknown roles for this compound in this subfamily. To identify gene products differentially expressed between luminescent and non-luminescent larvae, especially those associated with luciferase, SBF and keroplatin synthesis, here we compared the transcriptional and proteomic profiles of Neoditomyia sp., O. fultoni and Arachnocampa larvae and conducted biochemical assays. Similarly to O. fultoni, Neoditomyia sp. displays an abundance of hexamerin isoforms and transcripts associated with the tryptophan and kynurenine pathway, which is potentially involved with keroplatin synthesis and silk production. Despite displaying a similar electrophoretic pattern of Orfelia luciferase purified fractions, no luciferase activity was detected in Neoditomyia purified fractions. The SBF-enriched fractions from O. fultoni and Neoditomyia revealed a similar abundance of hexamerins, the presence of flavin-dependent reductases, keroplatin and riboflavin. The results indicate that the SBF consists of protein aggregates associated with riboflavin and keroplatin, which is used as luciferin in bioluminescent species and for other still unveiled physiological functions in non-luminescent species.
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).