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肿瘤坏死因子-α(TNFα)诱导人 p110δ 型 PI3K 异构体选择性表达:新型可诱导 PIK3CD 启动子的鉴定。

Isoform-selective induction of human p110δ PI3K expression by TNFα: identification of a new and inducible PIK3CD promoter.

机构信息

Centre for Cell Signalling, Barts Cancer Institute, Queen Mary University of London, Charterhouse Square, London EC1M 6BQ, UK.

出版信息

Biochem J. 2012 May 1;443(3):857-67. doi: 10.1042/BJ20112214.

Abstract

PI3Ks (phosphoinositide 3-kinases) are signalling molecules and drug targets with important biological functions, yet the regulation of PI3K gene expression is poorly understood. Key PI3Ks are the class IA PI3Ks that consist of a catalytic subunit (p110α, p110β and p110δ) in complex with a p85 regulatory subunit. Whereas p110α and p110β are ubiquitously expressed, high levels of p110δ are mainly found in white blood cells, with most non-leucocytes expressing low levels of p110δ. In the present paper we report that TNFα (tumour necrosis factor α) stimulation induces p110δ expression in human ECs (endothelial cells) and synovial fibroblasts, but not in leucocytes, through transcription start sites located in a novel promoter region in the p110δ gene (PIK3CD). This promoter is used in all cell types, including solid tumour cell lines that express p110δ, and is activated by TNFα in ECs and synovial fibroblasts. We further present a detailed biochemical and bioinformatic characterization of p110δ gene regulation, demonstrating that PIK3CD has distinct promoters, some of which can be dynamically activated by pro-inflammatory mediators. This is the first molecular identification of a PI3K promoter under the control of acute extracellular stimulation.

摘要

PI3Ks(磷酸肌醇 3-激酶)是信号分子和药物靶点,具有重要的生物学功能,但 PI3K 基因表达的调控机制仍知之甚少。关键的 PI3Ks 是 IA 类 PI3Ks,由一个催化亚基(p110α、p110β 和 p110δ)与一个 p85 调节亚基组成复合物。虽然 p110α 和 p110β 广泛表达,但 p110δ 的高水平主要存在于白细胞中,大多数非白细胞表达低水平的 p110δ。在本文中,我们报告 TNFα(肿瘤坏死因子 α)刺激通过位于 p110δ 基因(PIK3CD)中新启动子区域的转录起始位点,诱导人 ECs(内皮细胞)和滑膜成纤维细胞中 p110δ 的表达,但不能诱导白细胞中 p110δ 的表达。该启动子在所有细胞类型中均被使用,包括表达 p110δ 的实体瘤细胞系,并且在 ECs 和滑膜成纤维细胞中可被 TNFα 激活。我们进一步对 p110δ 基因调控进行了详细的生化和生物信息学分析,证明 PIK3CD 具有独特的启动子,其中一些启动子可被促炎介质动态激活。这是第一个受急性细胞外刺激调控的 PI3K 启动子的分子鉴定。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f349/3328000/c3c21b512a6b/bic012i001.jpg

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