Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
5
pubmed:dateCreated
2004-1-26
pubmed:abstractText
Over the past decade, a wealth of knowledge has been obtained concerning the mechanisms by which interferons (IFNs) and other cytokines activate or down-regulate immediate early genes via the Jak/Stat pathway. In contrast, little information is available on interferon-activated gene expression in naïve cells compared with cells that have been desensitized and subsequently resensitized to the actions of these cytokines. In naïve cells, the ISG54 gene is activated via IFN beta-stimulated formation of ISGF3, a heterotrimeric DNA binding complex consisting of p48 (IRF9) and tyrosine-phosphorylated Stat1 and Stat2. In contrast, in previously desensitized cells IFN beta weakly stimulates the assembly of an ISGF3-like complex that lacks Stat1, even though ISG54 mRNA induction is the same as in naïve cells. The lack of Stat1 tyrosine phosphorylation and DNA binding is due to increased activity of a protein-tyrosine phosphatase. In cells that do not express the tyrosine phosphatase Tc-PTP, the rate of Stat1 dephosphorylation is the same in naïve and previously desensitized cells. These results implicate Tc-PTP in a novel role in the regulation of type 1 interferon-stimulated gene expression.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Chromatin, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/IGSF3 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Immunoglobulins, http://linkedlifedata.com/resource/pubmed/chemical/Interferon Type I, http://linkedlifedata.com/resource/pubmed/chemical/Interferon-beta, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Proteins, http://linkedlifedata.com/resource/pubmed/chemical/PTPN2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatase..., http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatase..., http://linkedlifedata.com/resource/pubmed/chemical/Protein Tyrosine Phosphatases, http://linkedlifedata.com/resource/pubmed/chemical/Ptpn2 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/RNA, http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger, http://linkedlifedata.com/resource/pubmed/chemical/STAT1 Transcription Factor, http://linkedlifedata.com/resource/pubmed/chemical/STAT1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Stat1 protein, mouse, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Tyrosine
pubmed:status
MEDLINE
pubmed:month
Jan
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
30
pubmed:volume
279
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
3245-53
pubmed:dateRevised
2007-11-15
pubmed:meshHeading
pubmed-meshheading:14600148-Animals, pubmed-meshheading:14600148-Blotting, Western, pubmed-meshheading:14600148-Cell Line, pubmed-meshheading:14600148-Cell Nucleus, pubmed-meshheading:14600148-Cells, Cultured, pubmed-meshheading:14600148-Chromatin, pubmed-meshheading:14600148-Cytoplasm, pubmed-meshheading:14600148-DNA-Binding Proteins, pubmed-meshheading:14600148-Down-Regulation, pubmed-meshheading:14600148-Gene Expression Regulation, pubmed-meshheading:14600148-Humans, pubmed-meshheading:14600148-Immunoglobulins, pubmed-meshheading:14600148-Interferon Type I, pubmed-meshheading:14600148-Interferon-beta, pubmed-meshheading:14600148-Membrane Proteins, pubmed-meshheading:14600148-Mice, pubmed-meshheading:14600148-Phosphorylation, pubmed-meshheading:14600148-Precipitin Tests, pubmed-meshheading:14600148-Protein Binding, pubmed-meshheading:14600148-Protein Tyrosine Phosphatase, Non-Receptor Type 1, pubmed-meshheading:14600148-Protein Tyrosine Phosphatase, Non-Receptor Type 2, pubmed-meshheading:14600148-Protein Tyrosine Phosphatases, pubmed-meshheading:14600148-RNA, pubmed-meshheading:14600148-RNA, Messenger, pubmed-meshheading:14600148-STAT1 Transcription Factor, pubmed-meshheading:14600148-Time Factors, pubmed-meshheading:14600148-Trans-Activators, pubmed-meshheading:14600148-Tyrosine
pubmed:year
2004
pubmed:articleTitle
Cells previously desensitized to type 1 interferons display different mechanisms of activation of stat-dependent gene expression from naïve cells.
pubmed:affiliation
Department of Immunology, Lerner Research Institute, Cleveland Clinic Foundation, Ohio 44195, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't