抑制谷胱甘肽 S-转移酶基因 GSTd10 的表达可提高葫芦蝇对β-氯氰菊酯的敏感性。

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xiao-Di Zhai, Shi-Heng Wang, Meng Ma, Deng Pan, Jin-Jun Wang, Dong Wei
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引用次数: 0

摘要

Zeugodacus cucurbitae Coquillett(双翅目:Tephritidae)是世界上一种重要的农业和经济害虫,它对β-氯氰菊酯产生了抗药性。据报道,谷胱甘肽 S-转移酶(GST)参与了昆虫体内杀虫剂的解毒过程。我们在之前的研究中发现,ZcGSTd6和ZcGSTd10在β-氯氰菊酯的诱导下都会上调,因此本研究旨在探讨它们与β-氯氰菊酯耐受性的潜在关系。在大肠杆菌中异源表达的ZcGSTd6和ZcGSTd10对1-氯-2,4-二硝基苯(CDNB)具有显著的高活性。采用 Lineweaver-Burk 法测定了 ZcGSTd6 和 ZcGSTd10 的动力学参数。ZcGSTd6 的 Vmax 和 Km 分别为 0.50 μmol/min-mg 和 0.3 mM。ZcGSTd10 的 Vmax 和 Km 分别为 1.82 μmol/min-mg 和 0.53 mM。三维建模和分子对接结果表明,β-氯氰菊酯与ZcGSTd10活性位点SER-9的结合力更强。利用 RNA 干扰敲除 ZcGSTd6 和 ZcGSTd10 后,β-氯氰菊酯的敏感性分别显著增加了 18.73% 和 27.21%。此外,β-氯氰菊酯对 ZcGSTd10 的 CDNB 抑制率(IC50)和抑制常数(Ki)分别为 0.41 和 0.33 mM。没有分析β-氯氰菊酯对 ZcSGTd6 的 Ki 和 IC50。这些结果表明,ZcGSTd10可能是葫芦科植物耐受β-氯氰菊酯的重要调节因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Suppressing the expression of glutathione S-transferase gene GSTd10 increases the sensitivity of Zeugodacus cucurbitae against β-cypermethrin

Suppressing the expression of glutathione S-transferase gene GSTd10 increases the sensitivity of Zeugodacus cucurbitae against β-cypermethrin

Suppressing the expression of glutathione S-transferase gene GSTd10 increases the sensitivity of Zeugodacus cucurbitae against β-cypermethrin

Zeugodacus cucurbitae Coquillett (Diptera: Tephritidae) is an agriculturally and economically important pest worldwide that has developed resistance to β-cypermethrin. Glutathione S-transferases (GSTs) have been reported to be involved in the detoxification of insecticides in insects. We have found that both ZcGSTd6 and ZcGSTd10 were up-regulated by β-cypermethrin induction in our previous study, so we aimed to explore their potential relationship with β-cypermethrin tolerance in this study. The heterologous expression of ZcGSTd6 and ZcGSTd10 in Escherichia coli showed significantly high activities against 1-chloro-2,4-dinitrobenzene (CDNB). The kinetic parameters of ZcGSTd6 and ZcGSTd10 were determined by Lineweaver–Burk. The Vmax and Km of ZcGSTd6 were 0.50 μmol/min·mg and 0.3 mM, respectively. The Vmax and Km of ZcGSTd10 were 1.82 μmol/min·mg and 0.53 mM. The 3D modelling and molecular docking results revealed that β-cypermethrin exhibited a stronger bounding to the active site SER-9 of ZcGSTd10. The sensitivity to β-cypermethrin was significantly increased by 18.73% and 27.21%, respectively, after the knockdown of ZcGSTd6 and ZcGSTd10 by using RNA interference. In addition, the inhibition of CDNB at 50% (IC50) and the inhibition constants (Ki) of β-cypermethrin against ZcGSTd10 were determined as 0.41 and 0.33 mM, respectively. The Ki and IC50 of β-cypermethrin against ZcSGTd6 were not analysed. These results suggested that ZcGSTd10 could be an essential regulator involved in the tolerance of Z. cucurbitae to β-cypermethrin.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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