Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Type of study
Language
Publication year range
1.
Mol Immunol ; 44(13): 3364-79, 2007 Jul.
Article in English | MEDLINE | ID: mdl-17386941

ABSTRACT

Rapid induction of transcription is known to be mediated by factors which bind DNA following post-translational modification. We report here that non-tyrosine phosphorylated (NTP)-Stat1 is involved in a cooperative interaction with Spi-1/PU.1 and IRF8 to form a pre-associated, poised complex for IL1B gene induction. A double point mutation at a putative STAT binding site, which overlaps this composite Spi-1 x IRF8 site located in the LPS and IL-1 response element (LILRE), inhibited human IL1B LPS-dependent reporter activity to about 10 percent of the control wild type vector. Chromatin immunoprecipitation revealed stimulation-independent constitutive binding of IRF8, Spi-1 and NTP-Stat1 at the LILRE, while binding of C/EBP beta was activated at an adjacent C/EBP beta site after LPS stimulation. In contrast to Stat1, IRF8 was tyrosine phosphorylated following LPS treatment. Supporting the involvement of NTP-Stat1, LPS-induced IL1B reporter activity in monocytes was enhanced by ectopic expression of NTP-Stat1 Y701F. In contrast, co-expression of a Y211F IRF8 mutein functioned as a dominant-negative inhibitor of LPS-induced IL1B reporter activity. In vitro DNA binding using extracts from LPS-treated monocytes confirmed that the LILRE enhancer constitutively binds a trimolecular complex containing IRF8, Spi-1 and NTP-Stat1. Binding studies using in vitro-expressed proteins revealed that NTP-Stat1 enhanced the binding of Spi-1 and IRF8 to the LILRE. Co-expression of TRAF6, an LPS surrogate, with Spi-1 and IRF8 enhanced IL1B reporter activity in HEK293R cells, which was dramatically reduced when Y211F IRF8 was co-expressed. These results suggest that the rapid transcriptional induction of an important inflammatory gene is dependent upon constitutive cooperative binding of a Spi-1 x IRF8 x NTP-Stat1 complex to the LILRE, which primes the gene for immediate induction following IRF8 phosphorylation. Phosphorylation of chromatin pre-associated factors like IRF8 may be an important strategy for the rapid transcriptional activation of genes involved in innate immunity.


Subject(s)
Interferon Regulatory Factors/metabolism , Interleukin-1beta/biosynthesis , Interleukin-1beta/genetics , Lipopolysaccharides/immunology , Proto-Oncogene Proteins/metabolism , STAT1 Transcription Factor/physiology , Trans-Activators/metabolism , Transcriptional Activation/immunology , Animals , Cell Line , Cell Line, Tumor , Humans , Interferon Regulatory Factors/physiology , Mice , Phosphorylation , Protein Interaction Mapping , Proto-Oncogene Proteins/physiology , Response Elements , STAT1 Transcription Factor/metabolism , Trans-Activators/physiology , Transcription Factors/genetics , Transcription Factors/physiology , Transcriptional Activation/genetics , Tyrosine/metabolism
2.
Mol Immunol ; 43(7): 773-82, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16095699

ABSTRACT

Elucidating the role of glucocorticoid in regulating gene expression is crucial to developing effective strategies against inflammatory diseases such as arthritis. In this report we demonstrate that glucocorticoid inhibits transcription directed by the IL-lbeta gene (IL1B) upstream induction sequence (UIS) enhancer, and to a much lesser extent by the tissue-specific basal promoter. Within the enhancer, three transcription factor binding sites, previously demonstrated by us to be important for the induction of IL1B by lipopolysaccharide, are now shown to be directly inhibited by the synthetic glucocorticoid, dexamethasone. We also previously showed that one of these sites could bind a novel STAT-like factor, while the other two bound heterodimers containing NF-IL6(C/EBPbeta). Although it has been reported by others that NF-IL6 homodimers can interact with glucocorticoid receptor (GR) to enhance transcription of the alpha1-acid glycoprotein gene, it now appears that glucocorticoid represses DNA binding of NF-IL6 heterodimers as well as the novel STAT-like factor to the critical sites within the IL1B UIS. Thus, GR likely disrupts the DNA binding capability of critical IL1B factors via transrepression.


Subject(s)
Dexamethasone/pharmacology , Enhancer Elements, Genetic , Gene Expression Regulation/drug effects , Interleukin-1/genetics , Protein Precursors/genetics , Trans-Activators/antagonists & inhibitors , Binding Sites , CCAAT-Enhancer-Binding Protein-delta/antagonists & inhibitors , CCAAT-Enhancer-Binding Protein-delta/metabolism , Cells, Cultured , Chloramphenicol O-Acetyltransferase/analysis , Chloramphenicol O-Acetyltransferase/genetics , DNA/metabolism , Glucocorticoids/pharmacology , Humans , Lipopolysaccharides/pharmacology , RNA, Messenger/analysis , RNA, Messenger/metabolism , Signal Transduction , Trans-Activators/metabolism
SELECTION OF CITATIONS
SEARCH DETAIL
...