Li Gang, Niu Jin-Zhi, Zotti Moises, Sun Qin-Zhe, Zhu Lin, Zhang Jun, Liao Chong-Yu, Dou Wei, Wei Dan-Dan, Wang Jin-Jun, Smagghe Guy
Key Laboratory of Entomology and Pest Control Engineering, College of Plant Protection, Southwest University, Chongqing 400716, PR China; Academy of Agricultural Sciences, Southwest University, Chongqing 400716, PR China.
Molecular Entomology and Applied Bioinformatics, Department of Crop protection, Federal University of Pelotas, 96010-900, Pelotas, RS, Brazil.
Insect Biochem Mol Biol. 2017 Aug;87:136-146. doi: 10.1016/j.ibmb.2017.06.009. Epub 2017 Jun 20.
Ecdysteroids play a crucial role in regulating molting in the phylum of Arthropoda and much is known with members of the subphylum of Hexapoda including the Insecta. However, this is still unclear in key pests as spider mites belonging to the subphylum of Chelicerata that originated earlier in the Cambrian period. In this study, we investigated 14 key genes of ecdysteroid biosynthesis and signaling and their expression over the different developmental stages in the citrus red mite, Panonychus citri (Acari: Stigmaeidae). P. citri is an economically important and widespread pest of citrus crops and it has five developmental stages of egg, larva, protonymph, deutonymph and adult. Typically, the expression of the ecdysteroid-synthesizing Halloween gene Spook (PcSpo) followed a positive zigzag-like pattern with a peak in the first half of each developmental stage and a drop in the second half prior to the molting to the next stage. Similar to PcSpo, PcDib, PcSad, PcRXR2, PcE75 and PcHR38 showed a positive zigzag-like expression pattern, while that of PcE78, PcHR3 and PcFTZ-F1 was opposite that we called a negative zigzag-like pattern. Silencing of the PcSpo gene by RNAi showed that molting was inhibited. Interestingly, we could rescue these RNAi effects by supplementing ponasterone A (PonA) and not by 20E, which is indicative that mites use PonA rather than 20E as ecdysteroid hormone. Modeling of the ecdysteroid receptor (PcEcR) hormone binding cavity also predicted binding of PonA, but showed a steric hindrance for 20E. We believe our data provide insight into the evolution and expression patterns of key ecdysteroid biosynthesis and signaling genes in a distant, non-insect species, and can become a foundation to develop new targets for controlling important agricultural pests such as spider mites.
蜕皮甾类在节肢动物门的蜕皮调节中起着关键作用,对于包括昆虫纲在内的六足亚门成员,人们已经了解很多。然而,对于属于螯肢亚门且在寒武纪早期就已出现的关键害虫,如蜘蛛螨,情况仍不清楚。在本研究中,我们调查了柑橘全爪螨(叶螨科:柑橘全爪螨)蜕皮甾类生物合成和信号传导的14个关键基因及其在不同发育阶段的表达。柑橘全爪螨是柑橘作物上一种具有经济重要性且分布广泛的害虫,它有卵、幼虫、若螨、成螨五个发育阶段。通常,蜕皮甾类合成的“万圣节”基因Spook(PcSpo)的表达呈正锯齿状模式,在每个发育阶段的前半段达到峰值,在下一阶段蜕皮前的后半段下降。与PcSpo类似,PcDib、PcSad、PcRXR2、PcE75和PcHR38呈现正锯齿状表达模式,而PcE78、PcHR3和PcFTZ - F1则相反,我们称之为负锯齿状模式。通过RNA干扰沉默PcSpo基因表明蜕皮受到抑制。有趣的是,我们可以通过补充蜕皮甾酮(PonA)而非20E来挽救这些RNA干扰效应,这表明螨类使用PonA而非20E作为蜕皮甾类激素。对蜕皮甾类受体(PcEcR)激素结合腔的建模也预测了PonA的结合,但显示20E存在空间位阻。我们相信我们的数据为深入了解一种远缘非昆虫物种中关键蜕皮甾类生物合成和信号基因的进化及表达模式提供了见解,并可为开发控制蜘蛛螨等重要农业害虫的新靶点奠定基础。