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人类诱导型一氧化氮合酶基因通过核因子κB依赖性机制进行转录调控。

Human inducible nitric oxide synthase gene is transcriptionally regulated by nuclear factor-kappaB dependent mechanism.

作者信息

Nunokawa Y, Oikawa S, Tanaka S

机构信息

Suntory Institute for Biomedical Research, Osaka, Japan.

出版信息

Biochem Biophys Res Commun. 1996 Jun 14;223(2):347-52. doi: 10.1006/bbrc.1996.0897.

Abstract

We previously showed a sequence of the 5'-flanking region of the human inducible nitric oxide synthase (hiNOS) gene that included putative cis-acting elements. A reported plasmid containing the 5'-flanking region of the hiNOS gene upstream from its reporter gene was constructed, and then transiently or stably transfected into human cells known to express the hiNOS gene following cytokine stimulation. The transfected cells showed the inducibility of the reporter activity following interleukin-1beta stimulation. Reporter inducibility disappeared in cells transfected with a plasmid mutated in the putative nuclear factor (NF)-kappaB binding region. In addition the induction was inhibited by a treatment of anti-oxidant, pyrrolidinedithiocarbamate, known as an NF-kappaB inhibitor. Our results demonstrate that the promotor including the NF-kappaB region is functional and that the hiNOS gene is transcriptionally regulated via NF-kappaB activation in human cells.

摘要

我们先前展示了人类诱导型一氧化氮合酶(hiNOS)基因5'-侧翼区的一段序列,其中包含推定的顺式作用元件。构建了一个报告质粒,其包含hiNOS基因报告基因上游的5'-侧翼区,然后将其瞬时或稳定转染到已知在细胞因子刺激后表达hiNOS基因的人类细胞中。转染后的细胞在白细胞介素-1β刺激后表现出报告基因活性的诱导性。在用推定的核因子(NF)-κB结合区域发生突变的质粒转染的细胞中,报告基因诱导性消失。此外,用抗氧化剂吡咯烷二硫代氨基甲酸盐(一种已知的NF-κB抑制剂)处理可抑制诱导。我们的结果表明,包含NF-κB区域的启动子具有功能,并且hiNOS基因在人类细胞中通过NF-κB激活进行转录调控。

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