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核因子红系衍生2相关因子2响应植物化学物质和杀虫剂,激活斜纹夜蛾(鳞翅目:夜蛾科)中肠中的谷胱甘肽S-转移酶表达。

Nuclear factor erythroid-derived 2-related factor 2 activates glutathione S-transferase expression in the midgut of Spodoptera litura (Lepidoptera: Noctuidae) in response to phytochemicals and insecticides.

作者信息

Chen S, Lu M, Zhang N, Zou X, Mo M, Zheng S

机构信息

Guangzhou Key Laboratory of Insect Development Regulation and Applied Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal University, Guangzhou, China.

出版信息

Insect Mol Biol. 2018 Aug;27(4):522-532. doi: 10.1111/imb.12391. Epub 2018 May 10.

Abstract

Detoxication enzymes play an important role in insect resistance to xenobiotics such as insecticides and phytochemicals. We studied the pathway for activating the expression of glutathione S-transferases (GSTs) in response to selected xenobiotics. An assay of the promoter activity of GST epsilon 1 (Slgste1) of Spodoptera litura led to the discovery of a cis-regulating element. An antioxidant response element was activated in response to indole-3-carbinol (I3C) and chlorpyrifos (CPF) and was able to bind with the xenobiotic sensor protein nuclear factor erythroid-derived 2-related factor 2 (SlNrf2). SlNrf2 and Slgste1 were responsive to reactive oxygen species induced by I3C and CPF in a S. litura cell line, as well as in S. litura midguts. SlNrf2 RNA interference (RNAi) reduced the message RNA levels of Slgste1 and the peroxidase activity of GSTs in response to I3C, xanthotoxin, CPF and deltamethrin. SlNrf2 RNAi and inhibitor treatment of GST activity decreased the viability of I3C-treated cells. These results indicate that SlNrf2 activates the expression of GSTs in response to oxidative stresses caused by exposure to xenobiotics.

摘要

解毒酶在昆虫对杀虫剂和植物化学物质等异源生物的抗性中发挥着重要作用。我们研究了谷胱甘肽S-转移酶(GSTs)响应特定异源生物激活表达的途径。对斜纹夜蛾GST ε1(Slgste1)启动子活性的检测导致发现了一个顺式调控元件。抗氧化反应元件在响应吲哚-3-甲醇(I3C)和毒死蜱(CPF)时被激活,并能够与异源生物传感器蛋白核因子红系衍生2相关因子2(SlNrf2)结合。在斜纹夜蛾细胞系以及斜纹夜蛾中肠中,SlNrf2和Slgste1对I3C和CPF诱导的活性氧有反应。SlNrf2 RNA干扰(RNAi)降低了Slgste1的信使RNA水平以及GSTs对I3C、花椒毒素、CPF和溴氰菊酯的过氧化物酶活性。SlNrf2 RNAi和GST活性抑制剂处理降低了I3C处理细胞的活力。这些结果表明,SlNrf2响应接触异源生物引起的氧化应激激活GSTs的表达。

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