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细胞因子刺激的人诱导型一氧化氮合酶(iNOS)基因分析:人和小鼠iNOS启动子差异的特征

Analysis of the cytokine-stimulated human inducible nitric oxide synthase (iNOS) gene: characterization of differences between human and mouse iNOS promoters.

作者信息

Chu S C, Marks-Konczalik J, Wu H P, Banks T C, Moss J

机构信息

Pulmonary-Critical Care Medicine Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

Biochem Biophys Res Commun. 1998 Jul 30;248(3):871-8. doi: 10.1006/bbrc.1998.9062.

Abstract

Expression of human inducible nitric oxide synthase (hiNOS) is under cytokine control and is transcriptionally regulated. The hiNOS and mouse iNOS (miNOS) genes are regulated differently by cytokines. To understand better the transcriptional regulation of the hiNOS gene, the 8.3-kb hiNOS promoter was characterized. Promoter activity was evaluated by transient transfection of hiNOS luciferase constructs in A549 human alveolar type II epithelium-like cells in the presence and absence of cytokines (IFN-gamma, IL-1 beta, and TNF-alpha). Important cytokine-responsive elements are located at -3665 to -5574 bp (containing two perfectly matched AP-1 sites which are not present in miNOS promoter) and -8093 to -8296 bp (one perfectly matched NF-kappa B site) of the hiNOS promoter region. Likely, these two AP-1 sites and the upstream NF-kappa B site are important in the transcriptional induction of hiNOS by cytokines. Our data demonstrate the molecular basis for the different cytokine-stimulated characteristics of hiNOS and miNOS genes.

摘要

人诱导型一氧化氮合酶(hiNOS)的表达受细胞因子控制且存在转录调控。hiNOS基因和小鼠诱导型一氧化氮合酶(miNOS)基因受细胞因子的调控方式不同。为了更好地理解hiNOS基因的转录调控,对8.3 kb的hiNOS启动子进行了表征。通过在有和没有细胞因子(γ干扰素、白细胞介素-1β和肿瘤坏死因子-α)存在的情况下,将hiNOS荧光素酶构建体瞬时转染到A549人肺泡II型上皮样细胞中,评估启动子活性。重要的细胞因子反应元件位于hiNOS启动子区域的-3665至-5574 bp(包含两个完全匹配的AP-1位点,miNOS启动子中不存在)和-8093至-8296 bp(一个完全匹配的核因子κB位点)。这两个AP-1位点和上游核因子κB位点可能在细胞因子对hiNOS的转录诱导中起重要作用。我们的数据证明了hiNOS和miNOS基因不同的细胞因子刺激特性的分子基础。

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