东方果蛾蜕皮激素受体异构体(EcR)的分子特征和功能分析

IF 1.5 4区 农林科学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Archives of Insect Biochemistry and Physiology Pub Date : 2024-04-12 DOI:10.1002/arch.22110
Zhishan Cao, Olha Bakumenko, Volodymyr Vlasenko, Weihai Li, Jinjun Cao
{"title":"东方果蛾蜕皮激素受体异构体(EcR)的分子特征和功能分析","authors":"Zhishan Cao,&nbsp;Olha Bakumenko,&nbsp;Volodymyr Vlasenko,&nbsp;Weihai Li,&nbsp;Jinjun Cao","doi":"10.1002/arch.22110","DOIUrl":null,"url":null,"abstract":"<p>20-Hydroxyecdysone (20E) plays a vital role in a series of biological processes, via the nuclear receptors, EcR/USP by activating the ecdysone regulatory cascade. To clarify the role of EcR during the development of <i>Grapholita molesta</i>, the complementary DNA of ecdysone receptor isoform B1 (<i>GmEcR-B1</i>) was obtained from the transcriptome of <i>G. molesta</i> and verified by PCR. Alignment analysis revealed that the deduced protein sequence of GmEcR-B1 was highly homologous to EcR proteins identified in other lepidopteran species, especially the EcR-B1 isoform in <i>Spodoptera litura</i>. Quantitative real-time PCR showed that <i>GmEcRs</i> was expressed at all test developmental stages, and the expression level of <i>GmEcRs</i> was relatively higher during the period of the 3rd day of fifth instar larvae to 2nd of pupa than those in other stages. Moreover, the messenger RNA of <i>GmEcRs</i> was much more strongly expressed in the Malpighian tubule and epidermis than those in other tissues, which suggests that this gene may function in a tissue-specific manner during larval development. Silencing of <i>GmEcRs</i> could significantly downregulate the transcriptional level of ecdysone-inducible genes and result in increased mortality during metamorphosis and prolonged prepupal duration. Taken together, the present results indicate that <i>GmEcRs</i> may directly or indirectly affect the development of <i>G. molesta</i>.</p>","PeriodicalId":8281,"journal":{"name":"Archives of Insect Biochemistry and Physiology","volume":"115 4","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2024-04-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Molecular characterization and functional analysis of the ecdysone receptor isoform (EcR) from the oriental fruit moth Grapholita molesta (Lepidoptera: Tortricidae)\",\"authors\":\"Zhishan Cao,&nbsp;Olha Bakumenko,&nbsp;Volodymyr Vlasenko,&nbsp;Weihai Li,&nbsp;Jinjun Cao\",\"doi\":\"10.1002/arch.22110\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>20-Hydroxyecdysone (20E) plays a vital role in a series of biological processes, via the nuclear receptors, EcR/USP by activating the ecdysone regulatory cascade. To clarify the role of EcR during the development of <i>Grapholita molesta</i>, the complementary DNA of ecdysone receptor isoform B1 (<i>GmEcR-B1</i>) was obtained from the transcriptome of <i>G. molesta</i> and verified by PCR. Alignment analysis revealed that the deduced protein sequence of GmEcR-B1 was highly homologous to EcR proteins identified in other lepidopteran species, especially the EcR-B1 isoform in <i>Spodoptera litura</i>. Quantitative real-time PCR showed that <i>GmEcRs</i> was expressed at all test developmental stages, and the expression level of <i>GmEcRs</i> was relatively higher during the period of the 3rd day of fifth instar larvae to 2nd of pupa than those in other stages. Moreover, the messenger RNA of <i>GmEcRs</i> was much more strongly expressed in the Malpighian tubule and epidermis than those in other tissues, which suggests that this gene may function in a tissue-specific manner during larval development. Silencing of <i>GmEcRs</i> could significantly downregulate the transcriptional level of ecdysone-inducible genes and result in increased mortality during metamorphosis and prolonged prepupal duration. Taken together, the present results indicate that <i>GmEcRs</i> may directly or indirectly affect the development of <i>G. molesta</i>.</p>\",\"PeriodicalId\":8281,\"journal\":{\"name\":\"Archives of Insect Biochemistry and Physiology\",\"volume\":\"115 4\",\"pages\":\"\"},\"PeriodicalIF\":1.5000,\"publicationDate\":\"2024-04-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Archives of Insect Biochemistry and Physiology\",\"FirstCategoryId\":\"97\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/arch.22110\",\"RegionNum\":4,\"RegionCategory\":\"农林科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Archives of Insect Biochemistry and Physiology","FirstCategoryId":"97","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/arch.22110","RegionNum":4,"RegionCategory":"农林科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

20-羟基蜕皮激素(20E)通过核受体 EcR/USP 激活蜕皮激素调节级联,在一系列生物过程中发挥重要作用。为了明确蜕皮激素在石斑鱼发育过程中的作用,研究人员从石斑鱼的转录组中获得了蜕皮激素受体异构体 B1(GmEcR-B1)的互补 DNA,并通过 PCR 进行了验证。比对分析表明,GmEcR-B1的推导蛋白质序列与其他鳞翅目昆虫的蜕皮激素受体蛋白高度同源,尤其是与鞘翅目昆虫的蜕皮激素受体同工酶B1同源。实时定量 PCR 结果表明,GmEcRs 在所有试验发育阶段均有表达,其中五龄幼虫第 3 天至蛹第 2 天的表达水平相对高于其他阶段。此外,GmEcRs的信使RNA在马氏管和表皮的表达量远高于其他组织,这表明该基因在幼虫发育过程中可能以组织特异性的方式发挥作用。沉默 GmEcRs 可显著下调蜕皮激素诱导基因的转录水平,导致变态过程中死亡率增加和蛹前期持续时间延长。综上所述,本研究结果表明,GmEcRs 可能会直接或间接影响蜕皮鱼的发育。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

摘要图片

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Molecular characterization and functional analysis of the ecdysone receptor isoform (EcR) from the oriental fruit moth Grapholita molesta (Lepidoptera: Tortricidae)

20-Hydroxyecdysone (20E) plays a vital role in a series of biological processes, via the nuclear receptors, EcR/USP by activating the ecdysone regulatory cascade. To clarify the role of EcR during the development of Grapholita molesta, the complementary DNA of ecdysone receptor isoform B1 (GmEcR-B1) was obtained from the transcriptome of G. molesta and verified by PCR. Alignment analysis revealed that the deduced protein sequence of GmEcR-B1 was highly homologous to EcR proteins identified in other lepidopteran species, especially the EcR-B1 isoform in Spodoptera litura. Quantitative real-time PCR showed that GmEcRs was expressed at all test developmental stages, and the expression level of GmEcRs was relatively higher during the period of the 3rd day of fifth instar larvae to 2nd of pupa than those in other stages. Moreover, the messenger RNA of GmEcRs was much more strongly expressed in the Malpighian tubule and epidermis than those in other tissues, which suggests that this gene may function in a tissue-specific manner during larval development. Silencing of GmEcRs could significantly downregulate the transcriptional level of ecdysone-inducible genes and result in increased mortality during metamorphosis and prolonged prepupal duration. Taken together, the present results indicate that GmEcRs may directly or indirectly affect the development of G. molesta.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
CiteScore
4.30
自引率
4.50%
发文量
115
审稿时长
12 months
期刊介绍: Archives of Insect Biochemistry and Physiology is an international journal that publishes articles in English that are of interest to insect biochemists and physiologists. Generally these articles will be in, or related to, one of the following subject areas: Behavior, Bioinformatics, Carbohydrates, Cell Line Development, Cell Signalling, Development, Drug Discovery, Endocrinology, Enzymes, Lipids, Molecular Biology, Neurobiology, Nucleic Acids, Nutrition, Peptides, Pharmacology, Pollinators, Proteins, Toxicology. Archives will publish only original articles. Articles that are confirmatory in nature or deal with analytical methods previously described will not be accepted.
期刊最新文献
Microcystin-Lr-Induced Changes in Growth Performance, Intestinal Microbiota, and Lipid Metabolism of Black Soldier Fly Larvae (Hermetia illucens) Overexpression of Acetylation-Defective Heat Shock Protein 60 Inhibits the Proliferation of Nucleopolyhedrovirus in Bombyx mori Electroantennogram and Behavioral Responses of Nematus Hequensis Xiao Adult to Volatiles of Salix alba Leaves Recent Insights Into Insect Physiology and Biochemistry Omics Data Integration of Rhynchophorus Ferrugineus Reveals High-Potential Targeted Pathways for the Development of Pest Control Management
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1