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pubmed-article:11254713 a pubmed:Citation ;
	lifeskim:mentions umls-concept:C0019704 , umls-concept:C0679729 , umls-concept:C0021756 , umls-concept:C0085828 , umls-concept:C0040649 , umls-concept:C0879590 , umls-concept:C0086860 , umls-concept:C1167622 , umls-concept:C1145667 , umls-concept:C0439855 , umls-concept:C0205199 , umls-concept:C2825311 , umls-concept:C0013879 , umls-concept:C0392762 , umls-concept:C2349209 , umls-concept:C1705630 , umls-concept:C1515926 , umls-concept:C0961954 , umls-concept:C1100939 , umls-concept:C0205556 ;
	pubmed:issue "7" ;
	pubmed:dateCreated "2001-3-20" ;
	pubmed:abstractText "Dysregulation of cytokine secretion plays an important role in AIDS pathogenesis. Here, we demonstrate that expression of HIV-1 Tat protein in Jurkat cells induces a severe impairment of IL-2 but not TNF gene transcription. Interestingly, this inhibition correlates with the effect of the viral protein on the transactivation of the CD28RE/AP1 composite element (-164/-154), but not with that observed on the NFAT/AP1 site of the IL-2 gene promoter, neither with the effect on NF-kappa B- nor AP1-independent binding sites. Endogenous expression of Tat induced a decrease in the amount of the specific protein complex bound to the CD28RE/AP1 probe after PMA plus calcium ionophore stimulation. This effect was accompanied by qualitative alterations of the AP1 complex. Thus, in wild-type Jurkat cells, c-jun was absent from the complex, whereas in Tat-expressing cells, c-jun was increasingly recruited overtime. By contrast, similar amounts of c-rel and a small amount of NFAT1 were detected both in wild type and in Jurkat Tat(+) cells. Furthermore, Tat not only induced the participation of c-jun in the cooperative complex but also a decrease in its transactivation activity alone or in combination with c-rel. Thus, the interaction of Tat with the components of this rel/AP1 cooperative complex seems to induce quantitative and qualitative alterations of this complex as activation progresses, resulting in a decrease of IL-2 gene transcription. Altogether our results suggest the existence of tuned mechanisms that allow the viral protein to specifically affect cooperative interactions between transcription factors." ;
	pubmed:language "eng" ;
	pubmed:journal <http://linkedlifedata.com/resource/pubmed/journal/2985117R> ;
	pubmed:citationSubset "AIM" ;
	pubmed:chemical <http://linkedlifedata.com/resource/pubmed/chemical/Transcription+Factors> , <http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding+Proteins> , <http://linkedlifedata.com/resource/pubmed/chemical/Interleukin-2> , <http://linkedlifedata.com/resource/pubmed/chemical/Nuclear+Proteins> , <http://linkedlifedata.com/resource/pubmed/chemical/Gene+Products%2C+tat> , <http://linkedlifedata.com/resource/pubmed/chemical/tat+Gene+Products%2C+Human+Immunodeficiency+Virus> , <http://linkedlifedata.com/resource/pubmed/chemical/Antigens%2C+CD28> , <http://linkedlifedata.com/resource/pubmed/chemical/NF-kappa+B> , <http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene+Proteins+c-jun> , <http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene+Proteins+c-rel> , <http://linkedlifedata.com/resource/pubmed/chemical/Transcription+Factor+AP-1> , <http://linkedlifedata.com/resource/pubmed/chemical/NFATC+Transcription+Factors> , <http://linkedlifedata.com/resource/pubmed/chemical/NFATC2+protein%2C+human> ;
	pubmed:status "MEDLINE" ;
	pubmed:month "Apr" ;
	pubmed:issn "0022-1767" ;
	pubmed:author <http://linkedlifedata.com/resource/pubmed/author/Gonz%C3%A1lezEE> , <http://linkedlifedata.com/resource/pubmed/author/Gonz%C3%A1lezMM> , pubmed-author:FresnoMM , <http://linkedlifedata.com/resource/pubmed/author/Punz%C3%B3nCC> ;
	pubmed:issnType "Print" ;
	pubmed:day "1" ;
	pubmed:volume "166" ;
	pubmed:owner "NLM" ;
	pubmed:authorsComplete "Y" ;
	pubmed:pagination "4560-9" ;
	pubmed:dateRevised "2008-11-21" ;
	pubmed:meshHeading pubmed-meshheading:11254713-Humans , pubmed-meshheading:11254713-Animals , pubmed-meshheading:11254713-Kinetics , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Binding+Sites> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Nuclear+Proteins> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Transcription%2C+Genetic> , pubmed-meshheading:11254713-T-Lymphocytes , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Promoter+Regions%2C+Genetic> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-DNA-Binding+Proteins> , pubmed-meshheading:11254713-Down-Regulation , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Transcriptional+Activation> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Transcription+Factors> , pubmed-meshheading:11254713-Interleukin-2 , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-COS+Cells> , pubmed-meshheading:11254713-HIV-1 , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Gene+Products%2C+tat> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Antigens%2C+CD28> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Proto-Oncogene+Proteins+c-jun> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-tat+Gene+Products%2C+Human+Immunodeficiency+Virus> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-NF-kappa+B> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Proto-Oncogene+Proteins+c-rel> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-NFATC+Transcription+Factors> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Transcription+Factor+AP-1> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Jurkat+Cells> , <http://linkedlifedata.com/resource/pubmed/meshheading/11254713-Response+Elements> ;
	pubmed:year "2001" ;
	pubmed:articleTitle "HIV-1 Tat inhibits IL-2 gene transcription through qualitative and quantitative alterations of the cooperative Rel/AP1 complex bound to the CD28RE/AP1 composite element of the IL-2 promoter." ;
	pubmed:affiliation "Centro de Biología Molecular Severo Ochoa Consejo Superior de Investigaciones Cientificas-Universidad Autónoma de Madrid, Cantoblanco, Madrid, Spain." ;
	pubmed:publicationType "Journal Article" , "Research Support, Non-U.S. Gov't" .
