Abstract
The S1 species of mammalian reovirus mRNA, like a number of other viral but not cellular mRNAs, codes for two dissimilar polypeptides by initiation of translation at two 5'-proximal, out-of-frame AUG codons. To determine if uninfected cells can utilize bicistronic genes, a bovine papilloma virus-based vector system was used to select mouse C127 cell lines containing multiple integrated copies of the reovirus S1 gene. These cell lines produced both reovirus polypeptides from a single mRNA. In addition, studies of COS cells transfected with the S1 gene containing small changes around the first AUG suggest that bicistronic mRNA translation is regulated at the level of elongation. A model is proposed in which ribosomes engaged in translation of one reading frame interfere with movement of ribosomes in the other frame because of differences in codon usage. Expression of bicistronic genes may be similarly regulated in virus-infected cells.
MeSH Terms
Animals
Base Sequence
Cadmium/pharmacology
Cadmium Chloride
Cell Line
DNA, Viral/genetics
Gene Expression Regulation, Viral
Genes
Genetic Vectors
Mice
Molecular Sequence Data
Peptide Chain Elongation, Translational
Plasmids
Protein Biosynthesis/drug effects
RNA, Messenger/genetics
RNA, Viral/genetics
Reoviridae/genetics
Transfection
Viral Proteins/biosynthesis,genetics
Chemicals
DNA, Viral
RNA, Messenger
RNA, Viral
Viral Proteins
Cadmium
Cadmium Chloride
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Fajardo J E
Center for Advanced Biotechnology and Medicine, Piscataway, NJ 08854-5638.
Shatkin A J
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