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The nuclear-bound form of the progesterone receptor is generated through a hormone-dependent phosphorylation.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 1985 Aug 30; Vol. 131 (1), pp. 421-7. - Publication Year :
- 1985
-
Abstract
- The solubilized ("cytosolic") receptor present in the rabbit uterus in the absence of hormone and the chromatin-bound ("nuclear") receptor obtained after injection of a progestin were compared. Crude cellular extracts were analyzed by immunoblotting and receptors were purified by immunoaffinity chromatography. With both methods it was observed that the electrophoretic mobility of the "nuclear" receptor was slower than that of the "cytosolic" receptor. This difference in mobility appeared to be due to the existence of variably phosphorylated forms of receptor. The phosphorylation reaction was examined in uterine slices. In the absence of hormone the cytosolic receptor was phosphorylated. When hormone was added the phosphorylation of receptor was markedly enhanced and the electrophoretic mobility of the "nuclear" receptor was decreased. These experiments thus show that the receptor in its "cytosolic" form is a phosphoprotein. Under the effect of the hormone the receptor is further phosphorylated on some supplementary site(s). This polyphosphoprotein is the chromatin-bound, putatively active, form of the receptor. In this respect the intracellular progesterone receptor is similar to various membrane receptors for hormones and growth factors which are phosphorylated upon binding of their ligand.
- Subjects :
- Animals
Chromatography, Affinity
Cytosol metabolism
Electrophoresis, Polyacrylamide Gel
Female
Molecular Weight
Phosphorylation
Rabbits
Receptors, Progesterone drug effects
Cell Nucleus metabolism
Norpregnadienes pharmacology
Phosphoproteins metabolism
Promegestone pharmacology
Receptors, Progesterone metabolism
Uterus metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 0006-291X
- Volume :
- 131
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 4041184
- Full Text :
- https://doi.org/10.1016/0006-291x(85)91819-4