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鉴定 NCF2/p67phox 为 p53 的一个新靶基因。

Identification of NCF2/p67phox as a novel p53 target gene.

机构信息

Department of Experimental Medicine and Surgery, University of Tor Vergata, Rome, Italy.

出版信息

Cell Cycle. 2012 Dec 15;11(24):4589-96. doi: 10.4161/cc.22853. Epub 2012 Nov 27.

Abstract

Analysis of microarrays performed in p53-, TAp63α- and ΔNp63α-inducible SaOs-2 cell lines allowed the identification of NCF2 mRNA upregulation in response to p53 induction. NCF2 gene encodes for p67phox, the cytosolic subunit of the NADPH oxidase enzyme complex. The recruitment of p67phox to the cell membrane causes the activation of the NADPH oxidase complex followed by the generation of NADP+ and superoxide from molecular oxygen. The presence of three putative p53 binding sites on the NCF2 promoter was predicted, and the subsequent luciferase and chromatin immunoprecipitation assays showed the activation of NCF2 promoter by p53 and its direct binding in vivo to at least one of the sites, thus confirming the hypothesis. NCF2 upregulation was also confirmed by real-time PCR in several cell lines after p53 activation. NCF2 knockdown by siRNA results in a significant reduction of ROS production and stimulates cell death, suggesting a protective function of Nox2-generated ROS in cells against apoptosis. These results provide insight into the redox-sensitive signaling mechanism that mediates cell survival involving p53 and its novel target NCF2/p67phox.

摘要

在诱导表达 p53、TAp63α 和 ΔNp63α 的 SaOs-2 细胞系中进行的微阵列分析,鉴定出 NCF2 mRNA 对 p53 诱导的上调反应。NCF2 基因编码 NADPH 氧化酶酶复合物的胞质亚基 p67phox。p67phox 募集到细胞膜导致 NADPH 氧化酶复合物的激活,随后从分子氧产生 NADP+和超氧阴离子。预测 NCF2 启动子上存在三个假定的 p53 结合位点,随后的荧光素酶和染色质免疫沉淀测定显示 p53 对 NCF2 启动子的激活及其在体内与至少一个位点的直接结合,从而证实了这一假设。在 p53 激活后,几种细胞系中的实时 PCR 也证实了 NCF2 的上调。用 siRNA 敲低 NCF2 会导致 ROS 产生的显著减少,并刺激细胞死亡,这表明 Nox2 产生的 ROS 在细胞中对细胞凋亡具有保护作用。这些结果为涉及 p53 及其新靶标 NCF2/p67phox 的细胞存活的氧化还原敏感信号转导机制提供了深入了解。

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