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dc.creatorPocuca, N
dc.creatorRuzdijic, S
dc.creatorDemonacos, C
dc.creatorKanazir, D
dc.creatorKrstic-Demonacos, M
dc.date.accessioned2018-03-01T18:37:09Z
dc.date.available2018-03-01T18:37:09Z
dc.date.issued1998
dc.identifier.issn0960-0760 (print)
dc.identifier.urihttp://vinar.vin.bg.ac.rs/handle/123456789/2188
dc.description.abstractThe glucocorticoid receptor (GR) is a phosphoprotein and a member of the steroid/thyroid receptor superfamily of ligand dependent transcription factors. When the glucocorticoid receptor is expressed in yeast (Saccharomyces cerevisiae), it is competent for signal transduction and transcriptional regulation. We have studied the glucocorticoid receptor phosphorylation in yeast and demonstrated that the receptor is phosphorylated in both the absence and presence of hormone, on serine and threonine residues. This phosphorylation occurs within 15 min upon addition of radioactivity in both hormone treated and untreated cells. As reported for mammalian cells, additional phosphorylation occurs upon hormone binding and this phosphorylation is dependent on the type of the ligand. We have followed the hormone dependent receptor phosphorylation by electrophoretic mobility shift assay, and have shown that this mobility change is sensitive to phosphatase treatment. In addition, the appearance of hormone dependent phosphoisoforms of the receptor depends on the potency of the agonist used. Using this method we show that the residues contributing to the hormone dependent mobility shift are localized in one of the transcriptional activation domains, between amino acids 130-247. We altered the phosphorylation sites within this domain that correspond to the amino acids phosphorylated in mouse hormone treated cells. Using phosphopeptide maps we show that hormone changes the peptide pattern of metabolically labelled receptor, and we identify peptides which are phosphorylated in hormone dependent manner. Then we determine that phosphorylation of residues S224 and S232 is increased in the presence of hormone, whereas phosphorylation of residues T171 and S246 is constitutive. Finally, we show that in both yeast and mammalian cells the same residues on the glucocorticoid receptor are phosphorylated. Our results suggest that yeast cells would be a suitable system to study glucocorticoid receptor phosphorylation. The genetic manipulability of yeast cells, together with conservation of the phosphorylation of GR in yeast and mammalian cells and identification of hormone dependent phosphorylation, would facilitate the isolation of molecules involved in the glucocorticoid receptor phosphorylation pathway and further our understanding of this process. (C) 1998 Elsevier Science Ltd. All rights reserved.en
dc.rightsrestrictedAccessen
dc.sourceJournal of Steroid Biochemistry and Molecular Biologyen
dc.titleUsing yeast to study glucocorticoid receptor phosphorylationen
dc.typearticleen
dcterms.abstractПоцуца, Н; Руздијиц, С; Каназир, Д; Крстиц-Демонацос, М; Демонацос, Ц;
dc.citation.volume66
dc.citation.issue5-6
dc.citation.spage303
dc.citation.epage318
dc.identifier.wos000075747500005
dc.identifier.doi10.1016/S0960-0760(98)00057-0
dc.citation.rankM22
dc.identifier.pmid9749836
dc.identifier.scopus2-s2.0-0031788142


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