Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2003-6-5
pubmed:abstractText
Interferon-gamma (IFN-gamma) is required for induction of the human nitric oxide synthase-2 (NOS2) gene in lung epithelium. Although the human NOS2 promoter region contains many cytokine-responsive elements, the molecular basis of induction is only partially understood. Here, the major cis-regulatory elements that control IFN-gamma-inducible NOS2 gene transcription in human lung epithelial cells are identified as composite response elements that bind signal transducer and activator of transcription 1 (STAT-1) and activator protein 1 (AP-1), which is comprised of c-Fos, Fra-2, c-Jun, and JunD. Notably, IFN-gamma activation of the human NOS2 promoter is shown to require functional AP-1 regulatory region(s), suggesting a role for AP-1 activation/binding in the IFN-gamma induction of genes. We show that c-Fos interacts with STAT-1 after IFN-gamma activation and the c-Fos/STAT-1 complex binds to the gamma-activated site (GAS) element in close proximity to AP-1 sites located at 4.9 kb upstream of the transcription start site. Taken together, our findings support a model in which a physical interaction between c-Fos and STAT-1 participates in NOS2 gene transcriptional activation.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-gamma, http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-1, http://linkedlifedata.com/resource/pubmed/chemical/NOS2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase, http://linkedlifedata.com/resource/pubmed/chemical/Nitric Oxide Synthase Type II, http://linkedlifedata.com/resource/pubmed/chemical/Oligodeoxyribonucleotides, Antisense, http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins c-fos, http://linkedlifedata.com/resource/pubmed/chemical/STAT1 Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/STAT1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factor AP-1, http://linkedlifedata.com/resource/pubmed/chemical/Tumor Necrosis Factor-alpha
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1040-0605
pubmed:author
pubmed:issnType
Print
pubmed:volume
285
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
L137-48
pubmed:dateRevised
2011-10-27
pubmed:meshHeading
pubmed-meshheading:12788789-5' Flanking Region, pubmed-meshheading:12788789-Antineoplastic Agents, pubmed-meshheading:12788789-Base Sequence, pubmed-meshheading:12788789-Cells, Cultured, pubmed-meshheading:12788789-DNA-Binding Proteins, pubmed-meshheading:12788789-Enzyme Induction, pubmed-meshheading:12788789-Gene Expression Regulation, Enzymologic, pubmed-meshheading:12788789-Humans, pubmed-meshheading:12788789-Interferon-gamma, pubmed-meshheading:12788789-Interleukin-1, pubmed-meshheading:12788789-Molecular Sequence Data, pubmed-meshheading:12788789-Mutagenesis, pubmed-meshheading:12788789-Nitric Oxide Synthase, pubmed-meshheading:12788789-Nitric Oxide Synthase Type II, pubmed-meshheading:12788789-Oligodeoxyribonucleotides, Antisense, pubmed-meshheading:12788789-Promoter Regions, Genetic, pubmed-meshheading:12788789-Proto-Oncogene Proteins c-fos, pubmed-meshheading:12788789-Respiratory Mucosa, pubmed-meshheading:12788789-STAT1 Transcription Factor, pubmed-meshheading:12788789-Signal Transduction, pubmed-meshheading:12788789-Trans-Activators, pubmed-meshheading:12788789-Transcription Factor AP-1, pubmed-meshheading:12788789-Transcriptional Activation, pubmed-meshheading:12788789-Tumor Necrosis Factor-alpha
pubmed:year
2003
pubmed:articleTitle
STAT-1 and c-Fos interaction in nitric oxide synthase-2 gene activation.
pubmed:affiliation
Pulmonary and Critical Care Medicine and Cancer Biology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio 44195, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.