首页> 外文期刊>Molecular and Cellular Endocrinology >Orphan receptor Arp-1 binds to the nucleotide sequence located between TATA box and transcriptional initiation site of the human angiotensinogen gene and reduces estrogen induced promoter activity.
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Orphan receptor Arp-1 binds to the nucleotide sequence located between TATA box and transcriptional initiation site of the human angiotensinogen gene and reduces estrogen induced promoter activity.

机译:孤儿受体Arp-1与位于TATA盒和人类血管紧张素原基因转录起始位点之间的核苷酸序列结合,并降低雌激素诱导的启动子活性。

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摘要

Human angiotensinogen gene contains a C/A polymorphism at 20 bases upstream from the transcriptional initiation site. This sequence binds to the estrogen receptor when nucleoside A is present at this site and reporter constructs containing human angiotensinogen gene promoter with nucleoside A at -20 are transactivated on co-transfection of estrogen receptor in HepG2 cells followed by estrogen treatment. We show here that orphan receptor, Arp-1, which belongs to the COUP family of transcription factors also binds to this sequence. Co-transfection of Arp-1 reduces estrogen induced promoter activity of reporter constructs containing human angiotensinogen gene promoter. On the other hand co-transfection of Arp-1 does not have a significant effect on estrogen induced promoter activity of reporter constructs containing rat angiotensinogen gene promoter. Our data suggests that human and rat angiotensinogen genes are regulated in a different manner by estrogens.
机译:人血管紧张素原基因在转录起始位点上游20个碱基处具有C / A多态性。当在该位点存在核苷A时,该序列与雌激素受体结合,并且在HepG2细胞中共转染雌激素受体后,将含有人血管紧张素原基因启动子和-20核苷A的报告基因构建体激活,然后进行雌激素处理。我们在这里显示属于转录因子COUP家族的孤儿受体Arp-1也与该序列结合。 Arp-1的共转染降低了雌激素诱导的含有人血管紧张素原基因启动子的报告基因构建体的启动子活性。另一方面,Arp-1的共转染对含有大鼠血管紧张素原基因启动子的报告基因构建体的雌激素诱导的启动子活性没有显着影响。我们的数据表明,人类和大鼠血管紧张素原基因受到雌激素的调节不同。

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