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dc.contributor.authorTzavaras, T. J.en
dc.contributor.authorTsawdaroglou, N. H.en
dc.contributor.authorSekeris, C. E.en
dc.date.accessioned2015-11-24T19:09:31Z-
dc.date.available2015-11-24T19:09:31Z-
dc.identifier.issn0014-5793-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/20713-
dc.rightsDefault Licence-
dc.subjectAdrenalectomyen
dc.subjectAnimalsen
dc.subjectCell Nucleus/*metabolismen
dc.subjectCytosol/metabolismen
dc.subjectDexamethasone/metabolismen
dc.subjectGenesen
dc.subjectKineticsen
dc.subjectLiver/*metabolismen
dc.subjectMaleen
dc.subjectRatsen
dc.subjectRats, Inbred Strainsen
dc.subjectReceptors, Glucocorticoid/metabolism/*physiologyen
dc.subjectThymus Gland/*metabolismen
dc.subject*Transcription, Geneticen
dc.subjectTyrosine Transaminase/geneticsen
dc.titleInteraction of cytosol fractions containing activated glucocorticoid-receptor complexes from rat liver and thymus with heterologous nuclei: effects on transcriptionen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.secondaryhttp://www.ncbi.nlm.nih.gov/pubmed/2567681-
heal.identifier.secondaryhttp://ac.els-cdn.com/0014579389806787/1-s2.0-0014579389806787-main.pdf?_tid=7d393870b2edea89c758cd9b5f92b62d&acdnat=1333007613_66b9f83214856f56e72588b573d6322b-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Επιστημών Υγείας. Τμήμα Ιατρικήςel
heal.publicationDate1989-
heal.abstractTwo rat liver cytosol fractions containing activated glucocorticoid-receptor complexes are able to stimulate the transcriptional activity of rat liver nuclei; the respective fractions from the cytosol of thymocytes inhibit the capacity of thymus nuclei for RNA synthesis. A similar inhibitory effect on thymus nuclei is exerted by the presence of rat liver cytosol fractions. Spot hybridization using a tyrosine aminotransferase (TAT) probe demonstrates that TAT gene expression is stimulated by the liver cytosol fractions acting on homologous nuclei whereas it is inhibited, in thymus nuclei, by the addition of thymus cytosol fractions. No effect on transcription is observed if the liver or thymus cytosol is heat activated in the presence of the glucocorticoid antagonist, cortexolone. Treatment of liver nuclei, previously subjected to the action of thymus cytosol fractions with the respective liver ones, restores transcriptional activity to control or higher levels. We conclude that rat thymocyte nuclei and cytosol contain transcriptional factors, which in the presence of the glucocorticoid-receptor complex, irrespective of its source, inhibit gene expression, whereas in the absence of such factors, the glucocorticoid-receptor complex positively regulates the respective genes.en
heal.journalNameFEBS Letten
heal.journalTypepeer-reviewed-
heal.fullTextAvailabilityTRUE-
Appears in Collections:Άρθρα σε επιστημονικά περιοδικά ( Ανοικτά) - ΙΑΤ

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