Genomic structure and functional characterization of the promoter region of human IκB kinase-related kinase IKKi/IKKε gene

被引:23
|
作者
Wang, NZ [1 ]
Ahmed, S [1 ]
Haqqi, TM [1 ]
机构
[1] Case Western Reserve Univ, Dept Med, Div Rheumat Dis, Cleveland, OH 44106 USA
关键词
IKKi/IKK epsilon promoter; cis-acting element; transcriptional regulation; NF kappa B; chondrocyte;
D O I
10.1016/j.gene.2005.04.013
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The inducible I kappa B kinase (IKKi/IKK epsilon) is a recently described serine-threonine kinase that activates the transcription factors NF kappa B, interferon regulatory factor-3 (IRF3) and CCAAA/enhancer-binding protein (C/EBP delta). Several inflammatory agents have been shown to induce the expression of the IKKi gene in macrophages and other cell types but the mechanism is unknown. We have found that the IKKi expression was constitutive in human chondrocytes from OA cartilage and a human chondrocytic cell line C28/I2 but was up-regulated by the inflammatory cytokines TNF alpha or IL-1 beta in an NF kappa B-dependent manner. To understand the constitutive and inducible expression of the IKKi gene we localized the transcription start site (TSS), cloned and sequenced a 2 kb genomic DNA fragment 5' of the TSS and characterized the putative promoter region (PPR), and identified the motifs therein that are required for basal and cytokine-induced IKKi gene promoter activity. We found that IKKi core promoter was TATA-less and by using PCR generated deletion mutants of the PPR we found that the cis-elements responsible for basal transcriptional activity were located between -51 and -100 bp upstream of the TSS while the cytokine response elements were located distally between -501 and -1000 bp upstream of the TSS. The DNA region containing the cytokine response elements had two kappa B sites as the most relevant regulatory motifs. The results of site-directed mutagenesis revealed that the kappa B site located between -833 and -847 bp upstream of the TSS was biologically functional and required for cytokine-induced IKKi promoter activity in human chondrocytes and HeLa cells. The silence of the other kappa B site (-816/-802) was positional, rather than sequence-specific. Over-expression of NF kappa B p65 mimics the TNF alpha-induced activation of the IKKi promoter. Also the gel shift assay suggested that NF kappa B p65 is responsible for activation of the IKKi promoter. These data for the first time characterize the promoter region and provide further insights into the transcriptional regulation of IKKi in human chondrocytes and other cell types. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:118 / 133
页数:16
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