Beatty Joshua M, Smagghe Guy, Ogura Takehiko, Nakagawa Yoshiaki, Spindler-Barth Margarethe, Henrich Vincent C
Center for Biotechnology, Genomics, and Health Research, University of North Carolina at Greensboro, NC 27402, USA.
FEBS J. 2009 Jun;276(11):3087-98. doi: 10.1111/j.1742-4658.2009.07026.x. Epub 2009 Apr 22.
Insect development is driven by the action of ecdysteroids on morphogenetic processes. The classic ecdysteroid receptor is a protein heterodimer composed of two nuclear receptors, the ecdysone receptor (EcR) and Ultraspiracle (USP), the insect ortholog of retinoid X receptor. The functional properties of EcR and USP vary among insect species, and provide a basis for identifying novel and species-specific insecticidal candidates that disrupt this receptor's normal activity. A heterologous mammalian cell culture assay was used to assess the transcriptional activity of the heterodimeric ecdysteroid receptor from species representing two major insect orders: the fruit fly, Drosophila melanogaster (Diptera), and the Colorado potato beetle, Leptinotarsa decemlineata (Coleoptera). Several nonsteroidal agonists evoked a strong response with the L. decemlineata heterodimer that was consistent with biochemical and in vivo evidence, whereas the D. melanogaster receptor's response was comparatively modest. Conversely, the phytoecdysteroid muristerone A was more potent with the D. melanogaster heterodimer. The additional presence of juvenile hormone III potentiated the inductive activity of muristerone A in the receptors from both species, but juvenile hormone III was unable to potentiate the inductive activity of the diacylhydrazine methoxyfenozide (RH2485) in the receptor of either species. The effects of USP on ecdysteroid-regulated transcriptional activity also varied between the two species. When it was tested with D. melanogaster EcR isoforms, basal activity was lower and ligand-dependent activity was higher with L. decemlineata USP than with D. melanogaster USP. Generally, the species-based differences validate the use of the cell culture assay screen for novel agonists and potentiators as species-targeted insecticidal candidates.
昆虫发育受蜕皮甾体对形态发生过程的作用驱动。经典的蜕皮甾体受体是一种蛋白质异二聚体,由两种核受体组成,即蜕皮激素受体(EcR)和超气门蛋白(USP),后者是类视黄醇X受体的昆虫直系同源物。EcR和USP的功能特性在不同昆虫物种间存在差异,这为鉴定破坏该受体正常活性的新型且物种特异性杀虫候选物提供了依据。利用异源哺乳动物细胞培养试验评估了来自两个主要昆虫目的物种的异二聚体蜕皮甾体受体的转录活性:果蝇,黑腹果蝇(双翅目)和科罗拉多马铃薯甲虫,马铃薯甲虫(鞘翅目)。几种非甾体激动剂对马铃薯甲虫异二聚体引发了强烈反应,这与生化和体内证据一致,而黑腹果蝇受体的反应相对较弱。相反,植物蜕皮甾体muristerone A对黑腹果蝇异二聚体更有效。保幼激素III的额外存在增强了muristerone A在两种物种受体中的诱导活性,但保幼激素III无法增强双酰肼甲氧虫酰肼(RH2485)在任何一种物种受体中的诱导活性。USP对蜕皮甾体调节的转录活性的影响在这两个物种之间也有所不同。当用黑腹果蝇EcR亚型进行测试时,与黑腹果蝇USP相比,马铃薯甲虫USP的基础活性较低,配体依赖性活性较高。一般来说,基于物种的差异验证了使用细胞培养试验筛选新型激动剂和增强剂作为物种靶向杀虫候选物的可行性。