
Recently, a mammalian tRNA which was previously designated as an opal suppressor seryl-tRNA and phosphoseryl-tRNA was shown to be a selenocysteyl-tRNA (B. J. Lee, P. J. Worland, J. N. Davis, T. C. Stadtman, and D. Hatfield, J. Biol. Chem. 264:9724-9727, 1989). Hence, this tRNA is now designated as selenocysteyl-tRNA[Ser]Sec, and its function is twofold, to serve as (i) a carrier molecule upon which selenocysteine is biosynthesized and (ii) as a donor of selenocysteine, which is the 21st naturally occurring amino acid of protein, to the nascent polypeptide chain in response to specific UGA codons. In the present study, the selenocysteine tRNA gene was sequenced from Xenopus laevis, Drosophila melanogaster, and Caenorhabditis elegans. The tRNA product of this gene was also identified within the seryl-tRNA population of a number of higher and lower animals, and the human tRNA[Ser]Sec gene was used as a probe to identify homologous sequences within genomic DNAs of organisms throughout the animal kingdom. The studies showed that the tRNA[Ser]Sec gene has undergone evolutionary change and that it is ubiquitous in the animal kingdom. Further, we conclude that selenocysteine-containing proteins, as well as the use of UGA as a codon for selenocysteine, are far more widespread in nature than previously thought.
Base Sequence, Molecular Sequence Data, RNA, Transfer, Amino Acid-Specific, Biological Evolution, Selenocysteine, Blotting, Southern, Selenium, Xenopus laevis, Drosophila melanogaster, Suppression, Genetic, Genes, RNA, Transfer, Caenorhabditis, Animals, Nucleic Acid Conformation, Cysteine, Codon, Phylogeny
Base Sequence, Molecular Sequence Data, RNA, Transfer, Amino Acid-Specific, Biological Evolution, Selenocysteine, Blotting, Southern, Selenium, Xenopus laevis, Drosophila melanogaster, Suppression, Genetic, Genes, RNA, Transfer, Caenorhabditis, Animals, Nucleic Acid Conformation, Cysteine, Codon, Phylogeny
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