Transcript analysis of the selenoproteome indicates that dietary selenium requirements of rats based on selenium-regulated selenoprotein mRNA levels are uniformly less than those based on glutathione peroxidase activity.

Dietary selenium (Se) requirements in rats have been based largely upon glutathione peroxidase-1 (Gpx1) enzyme activity and Gpx1 mRNA levels can also be used to determine Se requirements. The identification of the complete selenoprotein proteome suggests that we might identify additional useful mole...

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Publicado en:Journal of Nutrition Vol. 139; no. 2; pp. 199 - 207
Autores principales: Barnes KM, Evenson JK, Raines AM, Sunde RA, Barnes, Kimberly M, Evenson, Jacqueline K, Raines, Anna M, Sunde, Roger A
Formato: research Journal Article
Publicado: Elsevier B.V. Feb2009
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb2009
      vid: 139
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      pub: Elsevier B.V.
      place: New York, New York
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        10.3945/jn.108.098624
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        atl: Transcript analysis of the selenoproteome indicates that dietary selenium requirements of rats based on selenium-regulated selenoprotein mRNA levels are uniformly less than those based on glutathione peroxidase activity.
      aug:
        au:
          Barnes KM
          Evenson JK
          Raines AM
          Sunde RA
          Barnes, Kimberly M
          Evenson, Jacqueline K
          Raines, Anna M
          Sunde, Roger A
        affil: Department of Nutritional Sciences, University of Wisconsin, Madison, WI 53706, USA
      sug:
        subj:
          Nutritional Requirements
          Oxidoreductases Metabolism
          Proteins
          Proteomics
          RNA
          Selenium Administration and Dosage
          Animals
          Male
          Rats
          Selenium Pharmacokinetics
          Male
      ab: Dietary selenium (Se) requirements in rats have been based largely upon glutathione peroxidase-1 (Gpx1) enzyme activity and Gpx1 mRNA levels can also be used to determine Se requirements. The identification of the complete selenoprotein proteome suggests that we might identify additional useful molecular biomarkers for assessment of Se status. To characterize Se regulation of the entire rat selenoproteome, weanling male rats were fed a Se-deficient diet (<0.01 microg Se/g) supplemented with graded levels of Se (0-0.8 microg/g diet) for 28 d, Se status was determined by tissue Se concentration and selenoenzyme activity, and selenoprotein mRNA abundance in liver, kidney, and muscle was determined by quantitative real-time-PCR. Tissue Se and selenoenzyme biomarkers indicated that minimal Se requirements were <or=0.1 microg Se/g diet for most biomarkers. Liver Gpx1 mRNA also decreased to <10% of Se-adequate levels, with a minimum Se requirement at 0.07 microg/g diet. Five selenoprotein mRNA in liver, 4 in kidney, and 2 in muscle decreased to <41% of Se-adequate levels, all with minimum Se requirements at <or=0.07 microg/g diet; the majority of selenoprotein mRNA in each tissue were not significantly regulated by Se status, and 1 selenoprotein, selenophosphate synthetase-2, was upregulated in Se-deficient kidney. Plateau breakpoints for all regulated selenoprotein mRNA were very similar, suggesting that 1 underlying mechanism is in play in Se regulation of selenoprotein mRNA. Lastly, we did not find any selenoprotein mRNA that could be used as biomarkers for super-nutritional/anticarcinogenic levels (up to 0.8 microg Se/g diet) of Se.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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