Research Institute of Applied Biology, Shanxi University, Taiyuan, Shanxi, China.
Modern Research Center For Traditional Chinese Medicine, Shanxi University, Taiyuan, Shanxi, China.
Pest Manag Sci. 2019 Nov;75(11):2916-2924. doi: 10.1002/ps.5600. Epub 2019 Sep 26.
The aryl hydrocarbon receptor (AhR) belongs to the bHLH-PAS (basic Helix-Loop-Helix - Period/ARNT/Single minded) family of transcription factors. AhR is a ligand-activated transcription factor, which participates in the sensing and transmitting stimuli of endogenous and exogenous chemicals, and subsequently activates the transcription of genes related to various physiological and detoxification functions.
In this study, a single full-length LmAhR sequence was cloned and characterized. RNA interference (RNAi) and insecticide bioassays showed that LmAhR plays a vital role in chlorpyrifos susceptibility. To better identify aryl hydrocarbon receptor from locusta migratoria (LmAhR)-regulated genes involved in chlorpyrifos susceptibility, a comparative transcriptome analysis was performed using double-stranded (ds)GFP- and dsLmAhR-injected Locusta migratoria. Differential gene expression analysis identified 145 down-regulated and 67 up-regulated genes (P ≤ 0.05 and fold change ≥2) in dsLmAhR-knockdown insects. We selected 27 down-regulated genes and verified their expression levels using reverse transcription quantitative PCR. Finally, one glutathione S-transferase (GST) gene (LmGSTd7) was selected as a candidate detoxification gene and was further validated via RNAi and chlorpyrifos bioassays.
Our data suggest that AhR is associated with chlorpyrifos susceptibility via the regulation of LmGSTd7 expression in L. migratoria. © 2019 Society of Chemical Industry.
芳香烃受体(AhR)属于碱性螺旋-环-螺旋-亮氨酸拉链(bHLH-PAS)家族转录因子。AhR 是一种配体激活的转录因子,参与内源性和外源性化学物质的感应和传递刺激,并随后激活与各种生理和解毒功能相关的基因的转录。
本研究克隆并鉴定了一个全长的 Lm AhR 序列。RNA 干扰(RNAi)和杀虫剂生物测定表明,Lm AhR 在毒死蜱敏感性中起着至关重要的作用。为了更好地识别与毒死蜱敏感性相关的拟除虫菊酯抗性的芳香烃受体,使用双链(ds)GFP 和 dsLm AhR 注射的 Locusta migratoria 进行了比较转录组分析。差异基因表达分析鉴定出 145 个下调和 67 个上调基因(P≤0.05,倍数变化≥2)在 dsLm AhR 敲低昆虫中。我们选择了 27 个下调基因,并使用反转录定量 PCR 验证了它们的表达水平。最后,选择一个谷胱甘肽 S-转移酶(GST)基因(LmGSTd7)作为候选解毒基因,并通过 RNAi 和毒死蜱生物测定进一步验证。
我们的数据表明,AhR 通过调节 L. migratoria 中的 LmGSTd7 表达与毒死蜱敏感性相关。 © 2019 化学工业协会。