{"title":"Transcription factor Nlci is essential for wing dimorphism in the brown planthopper, Nilaparvata lugens.","authors":"Dong Wen, He Jiang, Zhuangzhuang Qiao, Zewei Lu, Muhua Zhao, Miaomiao Tian, Shaoqin Li, Hongxia Hua","doi":"10.1111/1744-7917.70127","DOIUrl":null,"url":null,"abstract":"<p><p>The brown planthopper (BPH) alternatively develops into either macropterous or brachypterous morphs in response to environmental stimuli, enhancing its fitness and dispersal. Despite several key upstream regulator genes involved in wing morphs switching having been identified, the downstream pathways governing wing plasticity remain unclear. Here, we harvested the 4th instar nymphal wing buds from macropterous strain (MS) and brachypterous strain (BS) for transcriptome sequencing. Individually, 3 025 and 3 273 differentially expressed genes (DEGs) were identified in forewing and hindwing buds, respectively, between 2 strains. Functional enrichment analysis revealed that these DEGs were significantly enriched in various categories related to signal transduction and metabolism. Among these, the Hedgehog (Hh) pathway was implicated in environmental information processing and wing development regulating. Knocking down the transcription factor Cubitus interruptus (Nlci) of the Hh pathway significantly reduced the wing size and resulted in malformed wings of both strain adults. Additionally, the expression levels of downstream genes (Nlptc, Nlen, and Nldpp) were inhibited to varying degrees. Furthermore, the expression levels of Nlci and its downstream genes were decreased when injected with double-stranded (ds)NlInR1, but increased in dsNlInR2 treatment. Silencing of Nlci partially antagonized the acceleration effect of dsNlInR2 treatment on wing development, leading to an intermediate wing morph. Our findings expand the regulatory role of the Hh pathway in the wing dimorphism of BPH, providing new insights into the mechanisms underlying wing development.</p>","PeriodicalId":13618,"journal":{"name":"Insect Science","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-07-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/1744-7917.70127","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The brown planthopper (BPH) alternatively develops into either macropterous or brachypterous morphs in response to environmental stimuli, enhancing its fitness and dispersal. Despite several key upstream regulator genes involved in wing morphs switching having been identified, the downstream pathways governing wing plasticity remain unclear. Here, we harvested the 4th instar nymphal wing buds from macropterous strain (MS) and brachypterous strain (BS) for transcriptome sequencing. Individually, 3 025 and 3 273 differentially expressed genes (DEGs) were identified in forewing and hindwing buds, respectively, between 2 strains. Functional enrichment analysis revealed that these DEGs were significantly enriched in various categories related to signal transduction and metabolism. Among these, the Hedgehog (Hh) pathway was implicated in environmental information processing and wing development regulating. Knocking down the transcription factor Cubitus interruptus (Nlci) of the Hh pathway significantly reduced the wing size and resulted in malformed wings of both strain adults. Additionally, the expression levels of downstream genes (Nlptc, Nlen, and Nldpp) were inhibited to varying degrees. Furthermore, the expression levels of Nlci and its downstream genes were decreased when injected with double-stranded (ds)NlInR1, but increased in dsNlInR2 treatment. Silencing of Nlci partially antagonized the acceleration effect of dsNlInR2 treatment on wing development, leading to an intermediate wing morph. Our findings expand the regulatory role of the Hh pathway in the wing dimorphism of BPH, providing new insights into the mechanisms underlying wing development.
期刊介绍:
Insect Science is an English-language journal, which publishes original research articles dealing with all fields of research in into insects and other terrestrial arthropods. Papers in any of the following fields will be considered: ecology, behavior, biogeography, physiology, biochemistry, sociobiology, phylogeny, pest management, and exotic incursions. The emphasis of the journal is on the adaptation and evolutionary biology of insects from the molecular to the ecosystem level. Reviews, mini reviews and letters to the editor, book reviews, and information about academic activities of the society are also published.