Journal of Nutrition Animal Diets/Enrichment Products...

Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]
 QUICK SEARCH:   [advanced]


     


Journal of Nutrition Vol. 122 No. 8 August 1992, pp. 1620-1626
Copyright © 1992 by American Society for Nutrition
This Article
Right arrow Full Text (PDF)
Right arrow Purchase Article
Right arrow View Shopping Cart
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Christensen, M. J.
Right arrow Articles by Burgener, K. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Christensen, M. J.
Right arrow Articles by Burgener, K. W.

Dietary Selenium Stabilizes Glutathione Peroxidase mRNA in Rat Liver1,2,

Merrill J. Christensen and Kenneth W. Burgener

Department of Food Science and Nutrition, Brigham Young University, 475 WIDB, Provo, UT 84602

The objective of these studies was to determine the step at which dietary selenium (Se) regulates the pre-translational expression of the gene for cytosolic Se-glutathione peroxidase (Se-GPX) in rat liver. Weanling male Sprague-Dawley rats were fed a Torula yeast-based Se-deficient diet, or the same diet supplemented with 0.5 mg/kg as Na2SeO3, for at least 40 d. Livers were excised and divided into three portions for isolation of nuclei, for purification of total RNA and for assay of Se-GPX activity. Nuclei were used in run-on transcription assays and for isolation of total nuclear RNA. Nuclear RNA and total liver RNA were probed with segments from a rat Se-GPX cDNA in Northern blot and slot blot assays. Despite marked differences in Se-GPX activity, there were no significant differences between dietary groups in the transcription rates of the Se-GPX gene. Species hybridizing to Se-GPX were not detected in nuclear RNA. However, steady state levels of Se-GPX mRNA were markedly reduced by Se deficiency. These results suggest that dietary Se exerts its effect on pretranslational Se-GPX gene expression at the level of cytosolic mRNA stabilization.


KEY WORDS: • selenium • glutathione peroxidase • gene expression • rats • liver

1 Supported by NIH Grant no. DK41647 to M.J.C.

2 A report of these results was made at the Annual Meeting of the Federation of American Societies for Experimental Biology, April 21–25, 1991, Atlanta, GA [Christensen, M. J. & Burgener, K. W. (1991) Effect of selenium deficiency on gene transcription. FASEB J. 5: A579 (abs.)].

Manuscript received 7 October 1991. Revision accepted 14 April 1992.




This article has been cited by other articles:


Home page
Mol. Cell. Biol.Home page
J. E. Squires, I. Stoytchev, E. P. Forry, and M. J. Berry
SBP2 Binding Affinity Is a Major Determinant in Differential Selenoprotein mRNA Translation and Sensitivity to Nonsense-Mediated Decay
Mol. Cell. Biol., November 15, 2007; 27(22): 7848 - 7855.
[Abstract] [Full Text] [PDF]


Home page
Nucleic Acids ResHome page
P. R. Hoffmann, S. C. Hoge, P.-A. Li, F. W. Hoffmann, A. C. Hashimoto, and M. J. Berry
The selenoproteome exhibits widely varying, tissue-specific dependence on selenoprotein P for selenium supply
Nucleic Acids Res., June 9, 2007; 35(12): 3963 - 3973.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. Biol.Home page
L. A. de Jesus, P. R. Hoffmann, T. Michaud, E. P. Forry, A. Small-Howard, R. J. Stillwell, N. Morozova, J. W. Harney, and M. J. Berry
Nuclear Assembly of UGA Decoding Complexes on Selenoprotein mRNAs: a Mechanism for Eluding Nonsense-Mediated Decay?
Mol. Cell. Biol., March 1, 2006; 26(5): 1795 - 1805.
[Abstract] [Full Text] [PDF]




Home Help [Feedback] [For Subscribers] [Archive] [Search] [Contents]