Efficiency of mammalian selenocysteine incorporation

Anupama Mehta, Cheryl M. Rebsch, Scott A. Kinzyi, Julia E. Fletcher, Paul R. Copeland

Research output: Contribution to journalArticlepeer-review

71 Scopus citations

Abstract

Five components have thus far been identified that are necessary for the incorporation of selenocysteine (Sec) into ∼25 mammalian proteins. Two of these are cis sequences, a SECIS element in the 3′-untranslated region and a Sec codon (UGA) in the coding region. The three known trans-acting factors are a Sec-specific translation elongation factor (eEFSec), the Sec-tRNA Sec, and a SECIS-binding protein, SBP2. Here we describe a system in which the efficiency of Sec incorporation was determined quantitatively both in vitro and in transfected cells, and in which the contribution of each of the known factors is examined. The efficiency of Sec incorporation into a luciferase reporter system in vitro is maximally 5-8%, which is 6-10 times higher than that in transfected rat hepatoma cells, McArdle 7777. In contrast, the efficiency of Sec incorporation into selenoprotein P in vitro is ∼40%, suggesting that as yet unidentified cis-elements may regulate differential selenoprotein expression. In addition, we have found that SBP2 is the only limiting factor in rabbit reticulocyte lysate but not in transfected rat hepatoma cells where SBP2 is found to be mostly if not entirely cytoplasmic despite having a strong putative nuclear localization signal. The significance of these findings with regard to the function of known Sec incorporation factors is discussed.

Original languageEnglish (US)
Pages (from-to)37852-37859
Number of pages8
JournalJournal of Biological Chemistry
Volume279
Issue number36
DOIs
StatePublished - Sep 3 2004

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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