雌激素反应元件(ERE)样基序影响鳗鱼CYP1A基因的3-甲基胆蒽诱导。

Takao Itakura, Yukiko Ogino, Shyamal C Mahata, Mohamed A H El-Kady, Jun-Ya Aoki, Hironori Kato, Yoshio Kaminishi
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引用次数: 0

摘要

已知某些形式的细胞色素P450 (CYP)基因可由二恶英等外源性药物诱导。CYP1A基因的诱导是由芳烃受体(AHR)介导的,该受体与位于基因5'增强子区域的二恶英响应元件(DRE)的特定核苷酸序列结合。对鳗鱼CYP1A基因调控区域的功能分析表明,在基础启动子附近有一个654 bp的区域,不含DREs,但含有三个类似雌激素应答元件(ERE)半位的基序,对诱导表达有重要作用。考虑到非dre元素在CYP1A基因诱导中的重要性,我们使用点突变技术研究了ere样基序的作用。通过同时或单独在所有三个ERE半位点产生突变,鉴定了鳗鱼CYP1A基因的调控区域。在荧光素酶基因上游的表达载体上克隆了调控区,并将其微注射到水母卵中。采用竞争PCR法检测了3-甲基胆蒽(3-MC)处理饲料中外源荧光素酶在鳉鱼苗中的表达。所有三个ERE半位点的突变将表达降低到10%。突变的ERE(-2)或ERE(-3)减少50%的表达,而突变的ERE(-1)不影响诱导。鳗鱼CYP1A基因的两个功能半位点相互回文,似乎构成了完整的ere。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Estrogen-responsive element (ERE)-like motifs affect the 3-methylcholanthrene induction of eel CYP1A gene.

Some forms of cytochrome P450 (CYP) genes are known to be induced by xenobiotics such as dioxins. Induction of the CYP1A gene is mediated by an aryl hydrocarbon receptor (AHR) which binds to a specific nucleotide sequence called a dioxin-responsive element (DRE) located in the 5' enhancer region of the gene. Functional analysis of the regulatory region of the eel CYP1A gene had shown that a 654-bp region near the basal promoter, containing no DREs but three motifs that resemble estrogen-responsive element (ERE) halfsites, contributes substantially to the induced expression. Considering the importance of non-DRE elements in CYP1A gene induction, we investigated the role of ERE-like motifs using a point mutation technique. The regulatory region of the eel CYP1A gene was identified by creating mutations in all three ERE half-sites simultaneously or individually. The regulatory region constructs were cloned upstream of the luciferase gene in an expression vector which was microinjected into medaka ova. Expression of luciferase as a foreign gene in medaka fry exposed to 3-methylcholanthrene (3-MC)-treated feed was measured by competitive PCR analysis. Mutation in all the three ERE half-sites reduced expression to 10%. Mutation in ERE(-2) or ERE(-3) reduced the expression to 50%, whereas mutation in ERE(-1) did not affect the induction. The two functional half-sites of the eel CYP1A gene are palindromic to each other and appear to constitute the full-ERE.

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