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Regulation of ecdysteroid signalling during Drosophila development: identification characterization and modelling of ecdysone oxidase an enzyme involved in control of ligand concentration

机译:果蝇发育过程中蜕皮甾类信号传导的调节:蜕皮激素氧化酶的鉴定表征和建模该酶涉及控制配体浓度

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摘要

The steroidal moulting hormones (ecdysteroids) mediate developmental transitions in insects, and their regulation is mainly controlled by the production and inactivation of these steroid hormones at the appropriate developmental times. One route of metabolism of ecdysteroids in insects involves EO (ecdysone oxidase)-catalysed conversion into 3-dehydroecdysteroid, which undergoes reduction to the corresponding 3-epiecdysteroid. By a twin-stranded bioinformatics approach, employing both phylogenomics and model structure-based analysis, we first predicted that DmEO (the EO of Drosophila melanogaster) corresponds to the protein product of gene CG9504. When CG9504 was expressed in COS7 cells, significant conversion of ecdysone into 3-dehydroecdysone was observed. Quantitative PCR and enzyme assay showed that DmEO was mainly expressed in the midgut during the late instars at a time corresponding to a hormone titre peak. DmEO shares only 27% amino acid sequence identity with Spodoptera littoralis (Lepidoptera) EO, yet key substrate-binding residues are well conserved. A model of DmEO is consistent with an inability to catalyse reaction of cholesterol derivatives. The significance of DmEO in ligand activation is discussed in relation to new evidence suggesting that 3-dehydro- and 3-epiecdysteroids may be functionally active as ligands in a novel, atypical ecdysteroid signalling pathway involving the Drosophila orphan nuclear receptor, DHR38, rather than being merely hormone inactivation products.
机译:类固醇蜕皮激素(蜕皮类固醇)介导昆虫的发育过渡,其调节主要受这些类固醇激素在适当发育时期的产生和失活控制。蜕皮甾体在昆虫中的一种代谢途径涉及EO(蜕皮酮氧化酶)催化的转化为3-脱氢蜕皮甾体,然后还原为相应的3-表皮甾体。通过双链生物信息学方法,采用系统发育组学和基于模型结构的分析,我们首先预测DmEO(果蝇果蝇的EO)对应于基因CG9504的蛋白质产物。当CG9504在COS7细胞中表达时,观察到蜕皮激素显着转化为3-脱氢蜕皮激素。定量PCR和酶法测定表明,DmEO主要在晚熟期中肠中表达,时间对应于激素效价峰值。 DmEO与斜纹夜蛾(Lepidoptera)EO仅共享27%的氨基酸序列同一性,但关键的底物结合残基得到了很好的保守。 DmEO模型与无法催化胆固醇衍生物的反应是一致的。讨论了DmEO在配体激活中的重要性,并提出了新的证据,这些证据表明3-脱氢和3-表皮类固醇可能在涉及果蝇孤儿核受体DHR38的新型非典型类蜕皮类固醇信号通路中作为配体发挥功能。仅激素灭活产品。

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