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Pi类谷胱甘肽S-转移酶基因在斑马鱼中通过一种进化上保守的调控元件受Nrf 2调控。

Pi class glutathione S-transferase genes are regulated by Nrf 2 through an evolutionarily conserved regulatory element in zebrafish.

作者信息

Suzuki Takafumi, Takagi Yaeko, Osanai Hitoshi, Li Li, Takeuchi Miki, Katoh Yasutake, Kobayashi Makoto, Yamamoto Masayuki

机构信息

ERATO-JST and Institute of Basic Medical Sciences, Graduate School of Comprehensive Human Sciences, University of Tsukuba, Laboratory of Advanced Research D, Tsukuba 305-8577, Japan.

出版信息

Biochem J. 2005 May 15;388(Pt 1):65-73. doi: 10.1042/BJ20041860.

Abstract

Pi class GSTs (glutathione S-transferases) are a member of the vertebrate GST family of proteins that catalyse the conjugation of GSH to electrophilic compounds. The expression of Pi class GST genes can be induced by exposure to electrophiles. We demonstrated previously that the transcription factor Nrf 2 (NF-E2 p45-related factor 2) mediates this induction, not only in mammals, but also in fish. In the present study, we have isolated the genomic region of zebrafish containing the genes gstp1 and gstp2. The regulatory regions of zebrafish gstp1 and gstp2 have been examined by GFP (green fluorescent protein)-reporter gene analyses using microinjection into zebrafish embryos. Deletion and point-mutation analyses of the gstp1 promoter showed that an ARE (antioxidant-responsive element)-like sequence is located 50 bp upstream of the transcription initiation site which is essential for Nrf 2 transactivation. Using EMSA (electrophoretic mobility-shift assay) analysis we showed that zebrafish Nrf 2-MafK heterodimer specifically bound to this sequence. All the vertebrate Pi class GST genes harbour a similar ARE-like sequence in their promoter regions. We propose that this sequence is a conserved target site for Nrf 2 in the Pi class GST genes.

摘要

π类谷胱甘肽S-转移酶(GSTs)是脊椎动物GST蛋白家族的成员,可催化谷胱甘肽(GSH)与亲电化合物的结合。π类GST基因的表达可通过接触亲电试剂诱导产生。我们之前已证明,转录因子Nrf 2(NF-E2 p45相关因子2)不仅在哺乳动物中,而且在鱼类中都介导了这种诱导作用。在本研究中,我们分离出了斑马鱼中包含gstp1和gstp2基因的基因组区域。通过将绿色荧光蛋白(GFP)报告基因显微注射到斑马鱼胚胎中,对斑马鱼gstp1和gstp2的调控区域进行了分析。gstp1启动子的缺失和点突变分析表明,一个类似抗氧化反应元件(ARE)的序列位于转录起始位点上游50 bp处,这对于Nrf 2的反式激活至关重要。通过电泳迁移率变动分析(EMSA),我们发现斑马鱼Nrf 2-MafK异二聚体特异性结合该序列。所有脊椎动物的π类GST基因在其启动子区域都含有一个类似的ARE序列。我们认为该序列是π类GST基因中Nrf 2的保守靶位点。

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