Genomic structure and functional characterization of the promoter region of human IkappaB kinase-related kinase IKKi/IKKvarepsilon gene
Language: 
English
Abstract: 

The inducible IkappaB kinase (IKKi/IKKepsilon) is a recently described serine-threonine kinase that activates the transcription factors NFkappaB, interferon regulatory factor-3 (IRF3) and CCAAA/enhancer-binding protein (C/EBPdelta). 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 TNFalpha or IL-1betain an NFkappaB-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 kappaB sites as the most relevant regulatory motifs. The results of site-directed mutagenesis revealed that the kappaB 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 kappaB site (-816/-802) was positional, rather than sequence-specific. Over-expression of NFkappaB p65 mimics the TNFalpha-induced activation of the IKKi promoter. Also the gel shift assay suggested that NFkappaB 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.

Author(s): 
Wang, Naizhen
Ahmed, Salahuddin
Haqqi, Tariq M.
Item Type: 
Journal Article
Publication Title: 
Gene
Journal Abbreviation: 
Gene
Publication Date: 
Jun 20, 2005
Publication Year: 
2005
Pages: 
118-133
Volume: 
353
Issue: 
1
ISSN: 
0378-1119
DOI: 
10.1016/j.gene.2005.04.013
Library Catalog: 
NCBI Published Medical (?)
Extra: 
PMID: 15939554 PMCID: PMC1266289

Turabian/Chicago Citation

Naizhen Wang, Salahuddin Ahmed and Tariq M. Haqqi. Jun 20, 2005. "Genomic structure and functional characterization of the promoter region of human IkappaB kinase-related kinase IKKi/IKKvarepsilon gene." Gene 353: 1: 118-133. 10.1016/j.gene.2005.04.013.

Wikipedia Citation

<ref> {{Cite journal | doi = 10.1016/j.gene.2005.04.013 | issn = 0378-1119 | volume = 353 | pages = 118-133 | last = Wang | first = Naizhen | coauthors = Ahmed, Salahuddin, Haqqi, Tariq M. | title = Genomic structure and functional characterization of the promoter region of human IkappaB kinase-related kinase IKKi/IKKvarepsilon gene | journal = Gene | date = Jun 20, 2005 | pmid = | pmc = }} </ref>