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FTZ-F1和FOXL2通过与启动子基序特异性结合上调鲶鱼脑芳香化酶基因转录。

FTZ-F1 and FOXL2 up-regulate catfish brain aromatase gene transcription by specific binding to the promoter motifs.

作者信息

Sridevi P, Chaitanya R K, Dutta-Gupta Aparna, Senthilkumaran B

机构信息

Department of Animal Sciences, School of Life Sciences-Centre for Advanced Studies, University of Hyderabad, P.O. Central University, Hyderabad 500 046, Andhra Pradesh, India.

出版信息

Biochim Biophys Acta. 2012 Jan;1819(1):57-66. doi: 10.1016/j.bbagrm.2011.10.003. Epub 2011 Oct 14.

DOI:10.1016/j.bbagrm.2011.10.003
PMID:22019437
Abstract

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.

摘要

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、卵巢特异性的(cyp19a1a)和脑特异性的(cyp19a1b)cyp19基因。先前对硬骨鱼的研究表明,NR5A核受体亚家族以及叉头转录因子FOXL2对cyp19a1a表达具有调控作用。在本研究中,我们调查了腹鳍缺失因子1(FTZ-F1,一种NR5A亚家族成员)和FOXL2在呼吸空气的鲶鱼(非洲鲶鱼)脑中对cyp19a1b表达的调控作用。基于cyp19a1b、FTZ-F1和FOXL2在脑中的同步表达模式,我们分离了cyp19a1b的5'上游区域以分析调控基序。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启动子内其假定结合位点之一发生突变会消除这种效应。电泳凝胶迁移率变动实验表明,FTZ-F1和FOXL2蛋白与用作探针的合成放射性标记寡聚体结合,并且在加入各自抗体后迁移率发生变动。染色质免疫沉淀测定证实了这两种转录因子均与cyp

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