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人类核因子κB p50/p105基因的启动子。受核因子κB亚基和c-REL调控。

Promoter of the human NF-kappa B p50/p105 gene. Regulation by NF-kappa B subunits and by c-REL.

作者信息

Cogswell P C, Scheinman R I, Baldwin A S

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina, Chapel Hill 27599.

出版信息

J Immunol. 1993 Apr 1;150(7):2794-804.

PMID:8454856
Abstract

NF-kappa B is a transcription factor involved in the regulation of numerous genes encoding proteins involved in immune function, in inflammation or in cellular growth control. NF-kappa B is typically characterized as a heterodimer of a 50-kDa subunit (p50) and a 65-kDa (p65) subunit. Interestingly, the p50 subunit is derived by processing of a 105-kDa precursor. Induction of NF-kappa B DNA-binding activity involves both the release of cytoplasmically stored factor from its inhibitor known as I kappa B and the induction of NF-kappa B gene expression. We report here the cloning and functional analysis of the promoter of the p50/p105 NF-kappa B gene. Our data suggest the existence of multiple transcription initiation sites for this gene in the B cell line Raji, Jurkat T cells, and HeLa cells. The promoter is constitutively active in these cells and is inducible by phorbol ester and mitogen stimulation of Jurkat T cells. Expression of I kappa B inhibits this inducible activation of the p50/p105 promoter. Furthermore, we have shown that co-transfection of a p50/p105 promoter-reporter plasmid with expression vectors encoding the p50 or p65 subunits of NF-kappa B or c-Rel results in stimulation of gene expression. Supportive of the transfection data, we have identified a DNA-binding site for NF-kappa B in the promoter of the p50/p105 gene that is responsive only to a combination of p50 and p65. The data demonstrate that the p50/p105 NF-kappa B gene is regulated by members of the NF-kappa B/Rel family and likely by other important transcription factors.

摘要

核因子-κB是一种转录因子,参与调控众多编码免疫功能、炎症或细胞生长控制相关蛋白质的基因。核因子-κB通常被描述为一个50千道尔顿亚基(p50)和一个65千道尔顿(p65)亚基组成的异二聚体。有趣的是,p50亚基是由一个105千道尔顿前体加工而来。核因子-κB DNA结合活性的诱导既涉及从其抑制剂IκB中释放细胞质中储存的因子,也涉及核因子-κB基因表达的诱导。我们在此报告p50/p105核因子-κB基因启动子的克隆及功能分析。我们的数据表明,在B细胞系Raji、Jurkat T细胞和HeLa细胞中,该基因存在多个转录起始位点。该启动子在这些细胞中组成性激活,并可被佛波酯和Jurkat T细胞的丝裂原刺激诱导。IκB的表达抑制p50/p105启动子的这种诱导性激活。此外,我们已经表明,将p50/p105启动子-报告质粒与编码核因子-κB的p50或p65亚基或c-Rel的表达载体共转染会导致基因表达的刺激。支持转染数据的是,我们在p50/p105基因的启动子中鉴定出一个核因子-κB的DNA结合位点,该位点仅对p50和p65的组合有反应。数据表明,p50/p105核因子-κB基因受核因子-κB/Rel家族成员以及可能受其他重要转录因子的调控。

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