Dual effects of 2-deoxyglucose on synthesis of the glycoprotein hormone common alpha-subunit in butyrate-treated HeLa cells.
Open Access
- 1 May 1987
- journal article
- Published by Taylor & Francis in Molecular and Cellular Biology
- Vol. 7 (5) , 1592-1601
- https://doi.org/10.1128/mcb.7.5.1592
Abstract
Sodium butyrate (Btr) (3 mM) causes a 10-fold increase in production of the glycoprotein hormone alpha-subunit in HeLa cells. The following report demonstrates that this response could be inhibited about 95% by 5 mM 2-deoxy-D-glucose (dGlc), whereas alpha-subunit production in uninduced cells was affected little or not at all. Addition of D-mannose restored the Btr induction of Hela-alpha in cultures that had been treated with dGlc. When the alpha-subunits secreted by cells cultured in Btr plus dGlc or in Btr alone were compared by gel filtration (Sephadex G-75) and lectin affinity (concanavalin A and ricin) chromatography, differences were noted that probably reflect changes in their carbohydrate moieties. Immunoprecipitation of [35S]methionine-labeled HeLa-alpha and incubation with endoglycosidase H indicated that the subunit secreted from cells in the presence of dGlc contained oligosaccharide side chains that were not processed to the complex type. Cells that were simultaneously treated with Btr plus dGlc showed no increase in alpha-subunit production over cells receiving Btr only; in contrast, cells that were preincubated with Btr for either 16 or 36 h before dGlc was added exhibited high levels of subunit synthesis. Measurement of alpha-mRNA levels at various times after Btr and dGlc were added to cultures indicated that Btr brought about a dramatic increase in alpha-specific mRNA about 24 h after being added to cultures. This increase could be prevented by dGlc when added simultaneously with Btr but not when added after a 24-h preincubation. Although dGlc prevented the induction of alpha-subunit and alpha-mRNA in response to Btr, it had no effect on histone hyperacetylation, suggesting that if this chromatin modification is necessary for the induction process, it is not in itself sufficient. Together, the data demonstrate that dGlc inhibits the accumulation of alpha-subunit mRNA normally produced in response to Btr and that the subunit produced contains altered oligosaccharide constituents.Keywords
This publication has 42 references indexed in Scilit:
- Butyrate regulates glycosylation of the glycoprotein hormone alpha subunit secreted by “glucose-starved” human liver cellsBiochemical and Biophysical Research Communications, 1983
- Synthesis of the glycoprotein hormone .alpha. subunit and placental alkaline phosphatase by HeLa cells: effect of tunicamycin, 2-deoxyglucose, and sodium butyrateBiochemistry, 1981
- Nature of the difference in apparent molecular weights between the alpha subunit of urinary human chorionic gonadotropin and the alpha protein secreted by HeLa cellsBiochemical and Biophysical Research Communications, 1981
- Concentration-dependent effects of sodium butyrate in Chinese hamster cells: cell-cycle progression, inner-histone acetylation, histone H1 dephosphorylation, and induction of an H1-like proteinBiochemistry, 1980
- Isolation, cloning and sequence analysis of the cDNA for the α-subunit of human chorionic gonadotropinNature, 1979
- Formation of 2-Deoxyglucose-Containing Lipid-Linked Oligosaccharides. Interference with Glycosylation of GlycoproteinsEuropean Journal of Biochemistry, 1978
- Structure of chromatin containing extensively acetylated H3 and H4Cell, 1978
- Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase IJournal of Molecular Biology, 1977
- REVIEW THE BIOSYNTHESIS OF HORMONES BY NON-ENDOCRINE TUMOURS-A REVIEWJournal of Endocrinology, 1975
- Hormonal Effects of Nonendocrine TumorsAnnual Review of Medicine, 1965