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核因子-κB介导肿瘤坏死因子α诱导的视紫质神经元诱导蛋白(一种核因子-κB的负调节因子)的表达。

NF-kappaB mediates tumor necrosis factor alpha-induced expression of optineurin, a negative regulator of NF-kappaB.

作者信息

Sudhakar Cherukuri, Nagabhushana Ananthamurthy, Jain Nishant, Swarup Ghanshyam

机构信息

Centre for Cellular and Molecular Biology, Council of Scientific and Industrial Research, Hyderabad, India.

出版信息

PLoS One. 2009;4(4):e5114. doi: 10.1371/journal.pone.0005114. Epub 2009 Apr 2.

Abstract

Optineurin is a ubiquitously expressed multifunctional cytoplasmic protein encoded by OPTN gene. The expression of optineurin is induced by various cytokines. Here we have investigated the molecular mechanisms which regulate optineurin gene expression and the relationship between optineurin and nuclear factor kappaB (NF-kappaB). We cloned and characterized human optineurin promoter. Optineurin promoter was activated upon treatment of HeLa and A549 cells with tumor necrosis factor alpha (TNFalpha). Mutation of a putative NF-kappaB-binding site present in the core promoter resulted in loss of basal as well as TNFalpha-induced activity. Overexpression of p65 subunit of NF-kappaB activated this promoter through NF-kappaB site. Oligonucleotides corresponding to this putative NF-kappaB-binding site showed binding to NF-kappaB. TNFalpha-induced optineurin promoter activity was inhibited by expression of inhibitor of NF-kappaB (IkappaBalpha) super-repressor. Blocking of NF-kappaB activation resulted in inhibition of TNFalpha-induced optineurin gene expression. Overexpressed optineurin partly inhibited TNFalpha-induced NF-kappaB activation in Hela cells. Downregulation of optineurin by shRNA resulted in an increase in TNFalpha-induced as well as basal NF-kappaB activity. These results show that optineurin promoter activity and gene expression are regulated by NF-kappaB pathway in response to TNFalpha. In addition these results suggest that there is a negative feedback loop in which TNFalpha-induced NF-kappaB activity mediates expression of optineurin, which itself functions as a negative regulator of NF-kappaB.

摘要

视紫质是一种由OPTN基因编码的广泛表达的多功能细胞质蛋白。视紫质的表达受多种细胞因子诱导。在此,我们研究了调控视紫质基因表达的分子机制以及视紫质与核因子κB(NF-κB)之间的关系。我们克隆并鉴定了人视紫质启动子。用肿瘤坏死因子α(TNFα)处理HeLa和A549细胞后,视紫质启动子被激活。核心启动子中一个假定的NF-κB结合位点发生突变会导致基础活性以及TNFα诱导的活性丧失。NF-κB的p65亚基过表达通过NF-κB位点激活了该启动子。与这个假定的NF-κB结合位点对应的寡核苷酸显示出与NF-κB结合。NF-κB抑制剂(IkappaBalpha)超抑制剂的表达抑制了TNFα诱导的视紫质启动子活性。阻断NF-κB激活导致TNFα诱导的视紫质基因表达受到抑制。在Hela细胞中,过表达的视紫质部分抑制了TNFα诱导的NF-κB激活。用shRNA下调视紫质导致TNFα诱导的以及基础的NF-κB活性增加。这些结果表明,视紫质启动子活性和基因表达受NF-κB信号通路调控以响应TNFα。此外,这些结果表明存在一个负反馈环,其中TNFα诱导的NF-κB活性介导视紫质的表达,而视紫质本身作为NF-κB的负调节因子发挥作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cdcf/2660438/d80f64ec3146/pone.0005114.g001.jpg

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