首页> 外文期刊>Biochimica et Biophysica Acta. Gene Regulatory Mechanisms >FTZ-F1 and FOXL2 up-regulate catfish brain aromatase gene transcription by specific binding to the promoter motifs
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FTZ-F1 and FOXL2 up-regulate catfish brain aromatase gene transcription by specific binding to the promoter motifs

机译:FTZ-F1和FOXL2通过特异性结合启动子基序上调up鱼脑芳香化酶基因转录

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Cytochrome P450 aromatase (cyp19) catalyzes the conversion of androgens into estrogens. Teleosts have distinct, ovarian specific (cyp19a1a) and brain specific (cyp19a1b) cyp19 genes. Previous studies in teleosts demonstrated regulation of cyp19a1a expression by the NR5A nuclear receptor subfamily as well as a fork head transcription factor, FOXL2. In the present study, we investigated the involvement of fushi tarazu factor 1, FTZ-F1, a NR5A subfamily member, and FOXL2 in the regulation of cyp19a1b expression in brain of the air-breathing catfish, Clarias gariepinus. Based on the synchronous expression pattern of cyp19a1b, FTZ-F1 and FOXL2 in the brain, we isolated the 5' upstream region of cyp19a1b to analyse regulatory motifs. Promoter motif analysis revealed FTZ-F1/NR5A1 and FOXL2 binding nucleotide sequences. Transient transfection studies showed that FTZ-F1 and FOXL2 together enhanced the transcriptional activity of cyp19a1b gene in mammalian cell lines. Mutation in either of their putative binding sites within the cyp19a1b promoter abolished this effect. Electrophoretic gel mobility shift experiments indicated that FTZ-F1 and FOXL2 proteins bind to the synthesized radio-labelled oligomers used as probes and mobility shifted upon addition of their respective antibodies. Chromatin immunoprecipitation assay confirmed the binding of both these transcription factors to their corresponding cis-acting elements in the upstream region of cyp19a1b. To our knowledge, this study is the first report on the transcriptional regulation of cyp19a1b by FTZ-F1 and FOXL2 in a teleost fish.
机译:细胞色素P450芳香化酶(cyp19)催化雄激素转化为雌激素。硬骨鱼具有不同的卵巢特异性(cyp19a1a)和脑特异性(cyp19a1b)cyp19基因。先前在硬骨鱼中的研究表明,NR5A核受体亚家族以及叉头转录因子FOXL2对cyp19a1a表达的调节。在本研究中,我们调查了fushi tarazu因子1,FTZ-F1,NR5A亚家族成员和FOXL2与呼吸the鱼Clarias gariepinus脑中cyp19a1b表达的调节有关。基于cyp19a1b,FTZ-F1和FOXL2在大脑中的同步表达模式,我们分离了cyp19a1b的5'上游区域来分析调控基序。启动子基序分析揭示了FTZ-F1 / NR5A1和FOXL2结合核苷酸序列。瞬时转染研究表明FTZ-F1和FOXL2共同增强了cyp19a1b基因在哺乳动物细胞系中的转录活性。 cyp19a1b启动子中任一假定结合位点的突变均消除了这种作用。电泳迁移率迁移实验表明,FTZ-F1和FOXL2蛋白与用作探针的合成放射性标记低聚物结合,迁移率随着添加各自的抗体而发生迁移。染色质免疫沉淀测定法证实了这两个转录因子与cyp19a1b上游区域中相应的顺式作用元件结合。据我们所知,这项研究是关于硬骨鱼中FTZ-F1和FOXL2对cyp19a1b转录调控的首次报道。

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