Huiling Zhou, Wenjing Zhang, Jia Xu, Shuyan Feng, Peng Chen, Chengjun Li, Bin Li
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Functional validation experiments demonstrated that TcETHRA was the primary functional receptor. Both TcETH and TcETHRA promoted the shedding of the old cuticle, which was essential for successful molting, pupation, and eclosion. In addition, TcETH and TcETHRA specifically regulated female reproduction by influencing the expression of juvenile hormone acid methyltransferase (TcJHAMT3) and vitellogenin-related genes (TcVg1, TcVg2, and TcVgR). In contrast, knockdown of TcETHRB had no significant impact on development but significantly reduced female embryo hatchability. These findings clarify the functional divergence of receptor splice variants in insect development and reproduction, providing new insights into the plasticity of arthropod endocrine networks and potential targets for pest control strategies.</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":"{\"title\":\"Functional differentiation of ecdysis triggering hormone receptor variants in development and reproduction of Tribolium castaneum.\",\"authors\":\"Huiling Zhou, Wenjing Zhang, Jia Xu, Shuyan Feng, Peng Chen, Chengjun Li, Bin Li\",\"doi\":\"10.1111/1744-7917.70138\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Understanding the functional differentiation of hormone receptor variants is crucial for unraveling the complexity of endocrine regulatory networks and developing targeted pest management strategies. By integrating genetic manipulation with phenotypic analysis, we provided multiple lines of evidence for the distinct roles of ecdysis triggering hormone (ETH) receptor splice variants in the development and reproduction of Tribolium castaneum. The study revealed that the TcETH receptor gene was alternatively spliced into 2 variants, TcETHRA and TcETHRB, both of which were highly expressed in early and late pupae, early adults, and the central nervous system. The steroid hormone 20-hydroxyecdysone enhanced the expression of TcETH and its receptors via its nuclear receptor TcEcR. Functional validation experiments demonstrated that TcETHRA was the primary functional receptor. Both TcETH and TcETHRA promoted the shedding of the old cuticle, which was essential for successful molting, pupation, and eclosion. In addition, TcETH and TcETHRA specifically regulated female reproduction by influencing the expression of juvenile hormone acid methyltransferase (TcJHAMT3) and vitellogenin-related genes (TcVg1, TcVg2, and TcVgR). In contrast, knockdown of TcETHRB had no significant impact on development but significantly reduced female embryo hatchability. These findings clarify the functional divergence of receptor splice variants in insect development and reproduction, providing new insights into the plasticity of arthropod endocrine networks and potential targets for pest control strategies.</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/10.1111/1744-7917.70138\",\"RegionNum\":1,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENTOMOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Insect Science","FirstCategoryId":"97","ListUrlMain":"https://doi.org/10.1111/1744-7917.70138","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
Functional differentiation of ecdysis triggering hormone receptor variants in development and reproduction of Tribolium castaneum.
Understanding the functional differentiation of hormone receptor variants is crucial for unraveling the complexity of endocrine regulatory networks and developing targeted pest management strategies. By integrating genetic manipulation with phenotypic analysis, we provided multiple lines of evidence for the distinct roles of ecdysis triggering hormone (ETH) receptor splice variants in the development and reproduction of Tribolium castaneum. The study revealed that the TcETH receptor gene was alternatively spliced into 2 variants, TcETHRA and TcETHRB, both of which were highly expressed in early and late pupae, early adults, and the central nervous system. The steroid hormone 20-hydroxyecdysone enhanced the expression of TcETH and its receptors via its nuclear receptor TcEcR. Functional validation experiments demonstrated that TcETHRA was the primary functional receptor. Both TcETH and TcETHRA promoted the shedding of the old cuticle, which was essential for successful molting, pupation, and eclosion. In addition, TcETH and TcETHRA specifically regulated female reproduction by influencing the expression of juvenile hormone acid methyltransferase (TcJHAMT3) and vitellogenin-related genes (TcVg1, TcVg2, and TcVgR). In contrast, knockdown of TcETHRB had no significant impact on development but significantly reduced female embryo hatchability. These findings clarify the functional divergence of receptor splice variants in insect development and reproduction, providing new insights into the plasticity of arthropod endocrine networks and potential targets for pest control strategies.
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.