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首页> 外文期刊>BMC Biotechnology >The transcription factor Ap-1 regulates monkey 20α-hydroxysteroid dehydrogenase promoter activity in CHO cells
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The transcription factor Ap-1 regulates monkey 20α-hydroxysteroid dehydrogenase promoter activity in CHO cells

机译:转录因子Ap-1调节CHO细胞中的猴子20α-羟类固醇脱氢酶启动子活性

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Background Monkey 20α-hydroxysteroid dehydrogenase (20α-HSD) is a catabolic enzyme responsible for converting progesterone into biologically inactive 20α-hydroxyprogesterone, thereby playing a key role in the estrous cycle or pregnancy and allowing ovulation and parturition to occur in most mammalian animals. Monkey 20α-HSD was highly abundant in ovarian and placental tissues during the pre-ovulation and pre-parturition phase and was primarily localized in the syncytiotrophoblast of the placenta. In this study, we focused on the molecular characterization of the monkey 20α-HSD promoter region by conducting reporter assays in Chinese hamster ovary (CHO) K1 cells. Results A reporter assay using constructs of various lengths of the 5′-flanking region (-890-Luc, -513-Luc, -306-Luc, -273-Luc, and -70-Luc) revealed that a region corresponding to the activator protein 1 (Ap-1) located between -281 and -274?bp was essential for the transcriptional activity. Absence of the Ap-1 site in -273-Luc dramatically decreased the transcription levels to the control levels. When the reporter constructs were co-transfected with Ap-1 (Jun) and specificity protein (Sp-1) genes, the transcription activities of the constructs increased with the exception of -273 and -70, while that of the double construct was reduced compared to that of Ap-1 alone. Furthermore, mutational analysis demonstrated that a putative Ap-1 site played an important role in the expression of the reporter gene. These findings were confirmed by EMSA examining the interactions of the protein Ap-1 in a nuclear extract from CHO-K1 cells and the expression levels of the Ap-1 transcription factor in pre-parturition placenta and CHO-K1 cells. Although mut-1 and mut-2 of Ap-1 bound with nuclear extracts from CHO-K1 cells, the transcriptional activity of mut-3 was almost completely suppressed. Conclusions Our results indicate that the Ap-1 site (-281?→?-274) (5′-TGTCTCAT-3′) plays a crucial role in the activation of the monkey 20α-HSD gene. Thus, we demonstrated that monkey 20α-HSD promoter activity is regulated by the transcription factor Ap-1 in CHO-K1 cells.
机译:背景猴子20α-羟类固醇脱氢酶(20α-HSD)是一种分解代谢酶,负责将黄体酮转化为生物学上无活性的20α-羟基黄体酮,从而在发情周期或妊娠中起关键作用,并在大多数哺乳动物中发生排卵和分娩。猴子20α-HSD在排卵前和分娩前阶段在卵巢和胎盘组织中高度丰富,并且主要定位于胎盘的合体滋养层。在这项研究中,我们通过在中国仓鼠卵巢(CHO)K1细胞中进行报告基因分析,重点研究了猴子20α-HSD启动子区域的分子特征。结果使用多种长度的5'侧翼区域(-890-Luc,-513-Luc,-306-Luc,-273-Luc和-70-Luc)构建体进行的报告基因检测显示,与激活蛋白1(Ap-1)位于-281和-274?bp之间,对转录活性至关重要。 -273-Luc中不存在Ap-1位点,使转录水平明显降低至对照水平。当将报告构建体与Ap-1(Jun)和特异性蛋白(Sp-1)基因共转染时,除了-273和-70外,构建体的转录活性均增加,而双重构建体的转录活性则降低与单独的Ap-1相比。此外,突变分析表明推定的Ap-1位点在报告基因的表达中起重要作用。 EMSA检查了CHO-K1细胞核提取物中蛋白Ap-1的相互作用,以及分娩前胎盘和CHO-K1细胞中Ap-1转录因子的表达水平,证实了这些发现。尽管Ap-1的mut-1和mut-2与CHO-K1细胞的核提取物结合,但mut-3的转录活性几乎被完全抑制。结论我们的结果表明Ap-1位点(-281→→--274)(5′-TGTCTCAT-3′)在猴20α-HSD基因的激活中起着至关重要的作用。因此,我们证明了猴20α-HSD启动子活性受CHO-K1细胞中转录因子Ap-1的调节。

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