IDENTIFICATION OF A SELENOCYSTEYL-TRANSFER RNASER IN MAMMALIAN-CELLS THAT RECOGNIZES THE NONSENSE CODON, UGA

  • 15 June 1989
    • journal article
    • research article
    • Vol. 264  (17) , 9724-9727
Abstract
The presence of a unique opal suppressor seryl-tRNA in higher vertebrates which is converted to phosphoseryl-tRNA has been known for several years, but its function has been uncertain (see Hatfield, D. (1985) Trends Biochem. Sci. 10, 201-204 for review). In the present study, we demonstrate that this tRNA species also occurs in vivo as selenocysteyl-tRNASer suggesting that it functions both as a carrier molecule upon which selenocysteine is synthesized and as a direct selenocysteine donor to a growing polypeptide chain in response to specific UGA codons. [75Se]Seleno[3H]cysteyl-tRNASer formed by administering 75Se and [3H]serine to rat mammary tumor cells (TMT-081-MS) in culture was isolated from the cell extract. The amino acid attached to the tRNa was identified as selenocysteine following its deacylation and reaction with iodoacetate and 3-bromopropionate. The resulting alkyl derivatives co-chromatographed on an amino acid analyzer with authentic carboxymethylselenocysteine and carboxyethylselenocysteine. Seryl-tRNASer and phosphoseryl-tRNASer (Hatfield, D., Diamond, A., and Dudock, B. (1982) Proc. Natl. Acad. Sci. U. S. A. 79, 6215-6219), which co-migrate on a reverse phase chromatographic column with selenocysteyl-tRNASer, were also identified in extracts of TMT-018-MS cells. Hence, we propose that a metabolic pathway for selenocysteine synthesis in mammalian cells is the conversion of seryl-tRNASer via phosphoseryl-tRNASer to selenocysteyl-tRNASer. In a ribosomal binding assay selenocysteyl-tRNASer recognizes UGA but not any of the serine codons. Selenocysteyl-tRNASer is deacylated more readily than seryl-tRNASer (i.e. 58% deacylation during 15 min at pH 8.0 and 37.degree.C as compared to 41%).