Kaiyang Feng, Mingyu Zhao, Zhixin Jiang, Sihan Chen, Ya Yang, Qingying Chen, Xiang Wen, Lin Xu, Yuhan Yang, Zhifeng Xu, Jinzhi Niu, Wei Dou, Lin He
{"title":"角质层蛋白通过产生诱骗环状RNA介导蜘蛛螨抗逆性的进化","authors":"Kaiyang Feng, Mingyu Zhao, Zhixin Jiang, Sihan Chen, Ya Yang, Qingying Chen, Xiang Wen, Lin Xu, Yuhan Yang, Zhifeng Xu, Jinzhi Niu, Wei Dou, Lin He","doi":"10.1126/sciadv.ads3361","DOIUrl":null,"url":null,"abstract":"<div >Phytophagous mites, including <i>Tetranychus cinnabarinus</i>, are arthropods known for their wide infestation of host plants and pesticide resistance. We found that fenpropathrin-resistant female mites (YN-FeR, with target resistance: F1538I <i>kdr</i> mutation) exhibited significantly enhanced adaptability to various stress conditions, including exposure to different acaricides and high-temperature (34°C) and low-humidity environments (40% relative humidity). This evolution was attributed to cuticle thickening in resistant female mites. Cuticle protein <i>CPR25</i> was identified as a critical gene mediating cuticle thickening. <i>CPR25</i> regulated its own overexpression by producing a circular RNA, named <i>circCPR25</i>, which acted as a decoy to selectively sequester and bind to the miR-34~317 cluster. This study revealed a distinctive mechanism underlying the evolution of stress resistance in spider mites. Specifically, a cuticle protein in spider mites regulates its own overexpression by producing a decoy circRNA, thereby promoting cuticle thickening and facilitating rapid adaptation to adverse conditions.</div>","PeriodicalId":21609,"journal":{"name":"Science Advances","volume":"11 25","pages":""},"PeriodicalIF":11.7000,"publicationDate":"2025-06-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.science.org/doi/reader/10.1126/sciadv.ads3361","citationCount":"0","resultStr":"{\"title\":\"Cuticle protein mediates the evolution of stress resistance by generating a decoy circular RNA in spider mite\",\"authors\":\"Kaiyang Feng, Mingyu Zhao, Zhixin Jiang, Sihan Chen, Ya Yang, Qingying Chen, Xiang Wen, Lin Xu, Yuhan Yang, Zhifeng Xu, Jinzhi Niu, Wei Dou, Lin He\",\"doi\":\"10.1126/sciadv.ads3361\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div >Phytophagous mites, including <i>Tetranychus cinnabarinus</i>, are arthropods known for their wide infestation of host plants and pesticide resistance. We found that fenpropathrin-resistant female mites (YN-FeR, with target resistance: F1538I <i>kdr</i> mutation) exhibited significantly enhanced adaptability to various stress conditions, including exposure to different acaricides and high-temperature (34°C) and low-humidity environments (40% relative humidity). This evolution was attributed to cuticle thickening in resistant female mites. Cuticle protein <i>CPR25</i> was identified as a critical gene mediating cuticle thickening. <i>CPR25</i> regulated its own overexpression by producing a circular RNA, named <i>circCPR25</i>, which acted as a decoy to selectively sequester and bind to the miR-34~317 cluster. This study revealed a distinctive mechanism underlying the evolution of stress resistance in spider mites. Specifically, a cuticle protein in spider mites regulates its own overexpression by producing a decoy circRNA, thereby promoting cuticle thickening and facilitating rapid adaptation to adverse conditions.</div>\",\"PeriodicalId\":21609,\"journal\":{\"name\":\"Science Advances\",\"volume\":\"11 25\",\"pages\":\"\"},\"PeriodicalIF\":11.7000,\"publicationDate\":\"2025-06-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.science.org/doi/reader/10.1126/sciadv.ads3361\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Science Advances\",\"FirstCategoryId\":\"103\",\"ListUrlMain\":\"https://www.science.org/doi/10.1126/sciadv.ads3361\",\"RegionNum\":1,\"RegionCategory\":\"综合性期刊\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"MULTIDISCIPLINARY SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Science Advances","FirstCategoryId":"103","ListUrlMain":"https://www.science.org/doi/10.1126/sciadv.ads3361","RegionNum":1,"RegionCategory":"综合性期刊","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"MULTIDISCIPLINARY SCIENCES","Score":null,"Total":0}
Cuticle protein mediates the evolution of stress resistance by generating a decoy circular RNA in spider mite
Phytophagous mites, including Tetranychus cinnabarinus, are arthropods known for their wide infestation of host plants and pesticide resistance. We found that fenpropathrin-resistant female mites (YN-FeR, with target resistance: F1538I kdr mutation) exhibited significantly enhanced adaptability to various stress conditions, including exposure to different acaricides and high-temperature (34°C) and low-humidity environments (40% relative humidity). This evolution was attributed to cuticle thickening in resistant female mites. Cuticle protein CPR25 was identified as a critical gene mediating cuticle thickening. CPR25 regulated its own overexpression by producing a circular RNA, named circCPR25, which acted as a decoy to selectively sequester and bind to the miR-34~317 cluster. This study revealed a distinctive mechanism underlying the evolution of stress resistance in spider mites. Specifically, a cuticle protein in spider mites regulates its own overexpression by producing a decoy circRNA, thereby promoting cuticle thickening and facilitating rapid adaptation to adverse conditions.
期刊介绍:
Science Advances, an open-access journal by AAAS, publishes impactful research in diverse scientific areas. It aims for fair, fast, and expert peer review, providing freely accessible research to readers. Led by distinguished scientists, the journal supports AAAS's mission by extending Science magazine's capacity to identify and promote significant advances. Evolving digital publishing technologies play a crucial role in advancing AAAS's global mission for science communication and benefitting humankind.