{"title":"鳞翅目易化海藻糖转运体的复制所带来的代谢益处。","authors":"Tao Zhong, Guosheng Hua, Chaojie Chen, Guanwang Shen, Zhiqing Li, Xiaoting Hua, Ping Lin, Ping Zhao, Qingyou Xia","doi":"10.1111/1744-7917.70121","DOIUrl":null,"url":null,"abstract":"<p><p>In addition to being one of the primary processes for the formation and expansion of gene families, gene duplication also establishes the basis for the diversity and redundancy of gene functions, providing an abundance of genetic resources and a potent adaptive potential for biological evolution. Trehalose is a high-quality carbon source and blood sugar in insects. However, recent theoretical developments suggest that mechanisms for facilitated trehalose transport in lepidopteran insects remain relatively scarce. In this research, we identified, characterized, and analyzed the evolution of the facilitated trehalose transporter gene family in the silkworm. The results revealed that Bombyx mori and Spodoptera frugiperda experienced a significant expansion of the facilitated trehalose transporter gene (Tret) in Lepidoptera. Leveraging CRISPR/Cas9 gene editing technology, we altered BmTret60, the 60th member of this gene family, in the silkworm to investigate the gene's functional characteristics. Males and females of the BmTret60 mutant larvae were shown to exhibit a notable differentiation process in growth and developmental phases despite the fact that the larvae displayed basic viability. The silkworm's development process is influenced by BmTret60, a crucial member of the facilitated trehalose transporter gene family that controls metabolic equilibrium in fat body and hemolymph of terminal larvae. These results highlight the critical role that BmTret60, a member of the BmTret family, plays in preserving growth and homeostasis, as well as its possible role in preserving protein synthesis. Our research offers fresh perspectives on the critical function of the BmTret gene family in preserving metabolic homeostasis.</p>","PeriodicalId":13618,"journal":{"name":"Insect Science","volume":" ","pages":""},"PeriodicalIF":3.0000,"publicationDate":"2025-09-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Metabolic benefits conferred by duplication of the facilitated trehalose transporter in Lepidoptera.\",\"authors\":\"Tao Zhong, Guosheng Hua, Chaojie Chen, Guanwang Shen, Zhiqing Li, Xiaoting Hua, Ping Lin, Ping Zhao, Qingyou Xia\",\"doi\":\"10.1111/1744-7917.70121\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>In addition to being one of the primary processes for the formation and expansion of gene families, gene duplication also establishes the basis for the diversity and redundancy of gene functions, providing an abundance of genetic resources and a potent adaptive potential for biological evolution. Trehalose is a high-quality carbon source and blood sugar in insects. However, recent theoretical developments suggest that mechanisms for facilitated trehalose transport in lepidopteran insects remain relatively scarce. In this research, we identified, characterized, and analyzed the evolution of the facilitated trehalose transporter gene family in the silkworm. The results revealed that Bombyx mori and Spodoptera frugiperda experienced a significant expansion of the facilitated trehalose transporter gene (Tret) in Lepidoptera. Leveraging CRISPR/Cas9 gene editing technology, we altered BmTret60, the 60th member of this gene family, in the silkworm to investigate the gene's functional characteristics. Males and females of the BmTret60 mutant larvae were shown to exhibit a notable differentiation process in growth and developmental phases despite the fact that the larvae displayed basic viability. The silkworm's development process is influenced by BmTret60, a crucial member of the facilitated trehalose transporter gene family that controls metabolic equilibrium in fat body and hemolymph of terminal larvae. These results highlight the critical role that BmTret60, a member of the BmTret family, plays in preserving growth and homeostasis, as well as its possible role in preserving protein synthesis. Our research offers fresh perspectives on the critical function of the BmTret gene family in preserving metabolic homeostasis.</p>\",\"PeriodicalId\":13618,\"journal\":{\"name\":\"Insect Science\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.0000,\"publicationDate\":\"2025-09-08\",\"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/10.1111/1744-7917.70121\",\"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/10.1111/1744-7917.70121","RegionNum":1,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENTOMOLOGY","Score":null,"Total":0}
Metabolic benefits conferred by duplication of the facilitated trehalose transporter in Lepidoptera.
In addition to being one of the primary processes for the formation and expansion of gene families, gene duplication also establishes the basis for the diversity and redundancy of gene functions, providing an abundance of genetic resources and a potent adaptive potential for biological evolution. Trehalose is a high-quality carbon source and blood sugar in insects. However, recent theoretical developments suggest that mechanisms for facilitated trehalose transport in lepidopteran insects remain relatively scarce. In this research, we identified, characterized, and analyzed the evolution of the facilitated trehalose transporter gene family in the silkworm. The results revealed that Bombyx mori and Spodoptera frugiperda experienced a significant expansion of the facilitated trehalose transporter gene (Tret) in Lepidoptera. Leveraging CRISPR/Cas9 gene editing technology, we altered BmTret60, the 60th member of this gene family, in the silkworm to investigate the gene's functional characteristics. Males and females of the BmTret60 mutant larvae were shown to exhibit a notable differentiation process in growth and developmental phases despite the fact that the larvae displayed basic viability. The silkworm's development process is influenced by BmTret60, a crucial member of the facilitated trehalose transporter gene family that controls metabolic equilibrium in fat body and hemolymph of terminal larvae. These results highlight the critical role that BmTret60, a member of the BmTret family, plays in preserving growth and homeostasis, as well as its possible role in preserving protein synthesis. Our research offers fresh perspectives on the critical function of the BmTret gene family in preserving metabolic homeostasis.
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.