首页> 外文期刊>Biochimica et biophysica acta. Gene structure and expression >Analysis of the promoters for the β-esterase genes associated with insecticide resistance in the mosquito Culex quinquefasciatus
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Analysis of the promoters for the β-esterase genes associated with insecticide resistance in the mosquito Culex quinquefasciatus

机译:蚊库克斯库克斯蚊与杀虫剂抗性相关的β-酯酶基因启动子分析

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摘要

Resistance to organophosphorus (OP) insecticides in the mosquito Culex quinquefasciatus is primarily due to the amplification and over-expression of non-specific esterases. Co-amplification of two esterase genes, estα2~1 and estβ2~1, is the most common resistance genotype. In both resistant and susceptible mosquitoes the α- and β-esterase genes are oriented in a head-to-head arrangement, the intergenic sequences containing promoter elements for the divergent transcription of both esterases. Transient transfection of luciferase reporter gene constructs into a C. quinquefasciatus cell line was used to study these promoters. A control vector was constructed with the strong Drosophila actin 5c promoter driving expression of β-galactosidase. The β-esterase promoters from both insecticide resistant and -susceptible insects were highly active in directing luciferase expression. Transfections with panels of deletions revealed several regions where binding sites for positive and negative regulatory elements are located, and candidate transcription factor sites have been identified. Gel shift assays have identified one DNA-protein interaction that is stronger with the resistant than with the equivalent but slightly altered susceptible sequence. The arthropod initiator site TCAGT 135pp upstream of the ATG in both β-esterase promoters is essential for transcription initiation, but a putative TATA box is not involved.
机译:蚊子库克斯库克斯蚊中对有机磷(OP)杀虫剂的抗性主要是由于非特异性酯酶的扩增和过表达。两种酯酶基因estα2〜1和estβ2〜1的共扩增是最常见的耐药基因型。在抗性和易感性蚊子中,α-酯酶和β-酯酶基因都以头对头的方式排列,基因间序列包含用于两种酯酶发散转录的启动子元件。萤光素酶报道基因基因结构的瞬时转染入昆士革梭菌细胞系用于研究这些启动子。用强果蝇肌动蛋白5c启动子构建驱动β-半乳糖苷酶表达的对照载体。来自抗药性昆虫和易感昆虫的β-酯酶启动子在指导萤光素酶表达中具有很高的活性。用缺失组进行的转染揭示了几个区域,在这些区域中存在正调控元件和负调控元件的结合位点,并且已经鉴定出候选转录因子位点。凝胶位移测定法已经鉴定出一种DNA-蛋白质相互作用,该DNA-蛋白质相互作用具有比同等但略微改变的易感序列更强的抗性。在两个β-酯酶启动子中ATG上游节肢动物启动子位点TCAGT 135pp对于转录启动是必不可少的,但不涉及假定的TATA盒。

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