Zhi-long Niu , Jian Wei , Qian Wang , Yu-bo Yang , Ying-Nan Gao , Lu Li , Jia Jia , Wei Guo , Dan Zhao
{"title":"核糖核酸介导的核受体的敲低通过破坏几丁质代谢途径损害毛癣的角质层形成","authors":"Zhi-long Niu , Jian Wei , Qian Wang , Yu-bo Yang , Ying-Nan Gao , Lu Li , Jia Jia , Wei Guo , Dan Zhao","doi":"10.1016/j.jinsphys.2025.104861","DOIUrl":null,"url":null,"abstract":"<div><div>Nuclear receptors (NRs) are ligand-regulated transcription factors that play crucial roles in insect growth and development. However, their functions in <em>Holotrichia oblita</em> Faldermann remain uncharacterized. In this study, we identified and characterized three <em>HoNRs</em> from <em>H. oblita</em>. Spatiotemporal expression analysis revealed that all three <em>HoNRs</em> were predominantly expressed in eggs and first-instar larvae. Tissue localization showed high expression in the epidermis, fat body, and rectum. RNA interference (RNAi) experiments demonstrated that silencing these <em>HoNRs</em> reduced larval feeding, impaired molting, and resulted in a 37–50 % weight inhibition rate and a 73–93 % mortality rate. Hematoxylin-eosin staining showed that knockdown of <em>HoHR3</em>, <em>HoE75</em>, and <em>HoEcR</em> led to the formation of a thinner cuticle compared to controls, accompanied by a 46–48 % reduction in chitin content and downregulation of chitin metabolic Pathway genes. Additionally, the expression of these <em>HoNRs</em> was influenced by 20E at different time points. Therefore, these findings demonstrate that these three <em>HoNRs</em> are essential for normal molting in <em>H. oblita</em> through chitin metabolic pathway regulation.</div></div>","PeriodicalId":16189,"journal":{"name":"Journal of insect physiology","volume":"165 ","pages":"Article 104861"},"PeriodicalIF":2.3000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rnai-mediated knockdown of nuclear receptors impairs cuticle formation by disrupting chitin metabolic pathway in Holotrichia oblita\",\"authors\":\"Zhi-long Niu , Jian Wei , Qian Wang , Yu-bo Yang , Ying-Nan Gao , Lu Li , Jia Jia , Wei Guo , Dan Zhao\",\"doi\":\"10.1016/j.jinsphys.2025.104861\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Nuclear receptors (NRs) are ligand-regulated transcription factors that play crucial roles in insect growth and development. However, their functions in <em>Holotrichia oblita</em> Faldermann remain uncharacterized. In this study, we identified and characterized three <em>HoNRs</em> from <em>H. oblita</em>. Spatiotemporal expression analysis revealed that all three <em>HoNRs</em> were predominantly expressed in eggs and first-instar larvae. Tissue localization showed high expression in the epidermis, fat body, and rectum. RNA interference (RNAi) experiments demonstrated that silencing these <em>HoNRs</em> reduced larval feeding, impaired molting, and resulted in a 37–50 % weight inhibition rate and a 73–93 % mortality rate. Hematoxylin-eosin staining showed that knockdown of <em>HoHR3</em>, <em>HoE75</em>, and <em>HoEcR</em> led to the formation of a thinner cuticle compared to controls, accompanied by a 46–48 % reduction in chitin content and downregulation of chitin metabolic Pathway genes. Additionally, the expression of these <em>HoNRs</em> was influenced by 20E at different time points. Therefore, these findings demonstrate that these three <em>HoNRs</em> are essential for normal molting in <em>H. oblita</em> through chitin metabolic pathway regulation.</div></div>\",\"PeriodicalId\":16189,\"journal\":{\"name\":\"Journal of insect physiology\",\"volume\":\"165 \",\"pages\":\"Article 104861\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2025-07-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of insect physiology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0022191025001155\",\"RegionNum\":2,\"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":"Journal of insect physiology","FirstCategoryId":"97","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022191025001155","RegionNum":2,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
Rnai-mediated knockdown of nuclear receptors impairs cuticle formation by disrupting chitin metabolic pathway in Holotrichia oblita
Nuclear receptors (NRs) are ligand-regulated transcription factors that play crucial roles in insect growth and development. However, their functions in Holotrichia oblita Faldermann remain uncharacterized. In this study, we identified and characterized three HoNRs from H. oblita. Spatiotemporal expression analysis revealed that all three HoNRs were predominantly expressed in eggs and first-instar larvae. Tissue localization showed high expression in the epidermis, fat body, and rectum. RNA interference (RNAi) experiments demonstrated that silencing these HoNRs reduced larval feeding, impaired molting, and resulted in a 37–50 % weight inhibition rate and a 73–93 % mortality rate. Hematoxylin-eosin staining showed that knockdown of HoHR3, HoE75, and HoEcR led to the formation of a thinner cuticle compared to controls, accompanied by a 46–48 % reduction in chitin content and downregulation of chitin metabolic Pathway genes. Additionally, the expression of these HoNRs was influenced by 20E at different time points. Therefore, these findings demonstrate that these three HoNRs are essential for normal molting in H. oblita through chitin metabolic pathway regulation.
期刊介绍:
All aspects of insect physiology are published in this journal which will also accept papers on the physiology of other arthropods, if the referees consider the work to be of general interest. The coverage includes endocrinology (in relation to moulting, reproduction and metabolism), pheromones, neurobiology (cellular, integrative and developmental), physiological pharmacology, nutrition (food selection, digestion and absorption), homeostasis, excretion, reproduction and behaviour. Papers covering functional genomics and molecular approaches to physiological problems will also be included. Communications on structure and applied entomology can be published if the subject matter has an explicit bearing on the physiology of arthropods. Review articles and novel method papers are also welcomed.