Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
15
pubmed:dateCreated
1998-5-14
pubmed:databankReference
pubmed:abstractText
Selenium which occurs in proteins as the amino acid, selenocysteine, is essential for numerous biological processes and for human health. A prominent 75Se-labeled protein detected in human T-cells migrated as a 15-kDa band by SDS-polyacrylamide gel electrophoresis. This protein subunit was purified and subjected to tryptic digestion and peptide sequence analyses. Sequences of tryptic peptides derived from the protein corresponded to a human placental gene sequence containing an open reading frame of 162 residues and a readthrough in-frame TGA codon. Three different peptide sequences of the 15-kDa protein corresponded to a nucleotide sequence located downstream of this codon, suggesting that the T-cell 15-kDa selenoprotein contains a selenocysteine residue encoded by TGA. Post-translational processing of the N-terminal portion of the predicted gene product to give the 15-kDa protein was suggested on the basis of molecular mass, amino acid analysis, and immunoblot assays of the purified protein. The 3'-untranslated region (UTR) of the gene encoding the 15-kDa protein contained a sequence that is very similar to the canonical selenocysteine-inserting sequence element. Computer analysis of transcript map data bases indicated that this gene was located on human chromosome 1. Its coding sequence showed no homology to known protein-encoding genes. The 15-kDa protein gene was expressed as mRNA in a wide range of tissues, with increased levels in the thyroid, parathyroid, and prostate-derived cells as evidenced by searches of partial cDNA sequences in public data bases. Genes corresponding to the 15-kDa selenocysteine-containing protein were found in mice and rats, while the corresponding genes in Caenorhabditis elegans and Brugia malayi contained a cysteine codon in place of TGA. The discovery of a new human selenoprotein provides an additional example of the role of selenium in mammalian systems.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Apr
pubmed:issn
0021-9258
pubmed:author
pubmed:issnType
Print
pubmed:day
10
pubmed:volume
273
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
8910-5
pubmed:dateRevised
2005-11-17
pubmed:meshHeading
pubmed-meshheading:9535873-Amino Acid Sequence, pubmed-meshheading:9535873-Animals, pubmed-meshheading:9535873-Base Sequence, pubmed-meshheading:9535873-Brugia malayi, pubmed-meshheading:9535873-Caenorhabditis elegans, pubmed-meshheading:9535873-Cell Line, pubmed-meshheading:9535873-Chromosome Mapping, pubmed-meshheading:9535873-Chromosomes, Human, Pair 1, pubmed-meshheading:9535873-DNA, Complementary, pubmed-meshheading:9535873-Gene Library, pubmed-meshheading:9535873-Humans, pubmed-meshheading:9535873-Jurkat Cells, pubmed-meshheading:9535873-Male, pubmed-meshheading:9535873-Mice, pubmed-meshheading:9535873-Models, Molecular, pubmed-meshheading:9535873-Molecular Sequence Data, pubmed-meshheading:9535873-Molecular Weight, pubmed-meshheading:9535873-Neoplasms, pubmed-meshheading:9535873-Organ Specificity, pubmed-meshheading:9535873-Peptide Fragments, pubmed-meshheading:9535873-Peptide Mapping, pubmed-meshheading:9535873-Protein Biosynthesis, pubmed-meshheading:9535873-Protein Structure, Secondary, pubmed-meshheading:9535873-Proteins, pubmed-meshheading:9535873-Rats, pubmed-meshheading:9535873-Recombinant Proteins, pubmed-meshheading:9535873-Selenium, pubmed-meshheading:9535873-Selenium Radioisotopes, pubmed-meshheading:9535873-Selenoproteins, pubmed-meshheading:9535873-Sequence Alignment, pubmed-meshheading:9535873-Sequence Homology, Amino Acid, pubmed-meshheading:9535873-T-Lymphocytes, pubmed-meshheading:9535873-Transcription, Genetic
pubmed:year
1998
pubmed:articleTitle
A new human selenium-containing protein. Purification, characterization, and cDNA sequence.
pubmed:affiliation
Section on the Molecular Biology of Selenium, Basic Research Laboratory, NCI, National Institutes of Health, Bethesda, Maryland 20892, USA.VNG@unlinfo2.unl.edu
pubmed:publicationType
Journal Article