Aberrant glycoprotein mRNA synthesized by the internal deletion mutant of vesicular stomatitis virus
Author(s) -
Ronald C. Herman,
Robert A. Lazzarini
Publication year - 1981
Publication title -
journal of virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.617
H-Index - 292
eISSN - 1070-6321
pISSN - 0022-538X
DOI - 10.1128/jvi.40.1.78-86.1981
Subject(s) - biology , polyadenylation , microbiology and biotechnology , transcription (linguistics) , vesicular stomatitis virus , messenger rna , rna polymerase ii , mutant , rhabdoviridae , rna , glycoprotein , polymerase , rna polymerase , gene , virology , gene expression , virus , promoter , genetics , linguistics , philosophy
The internal deletion mutant (DI-LT) derived from the heat-resistant strain of vesicular stomatitis virus synthesized an aberrant polyadenylated mRNA in vivo and in vitro. No normal glycoprotein message could be detected among the in vivo transcription products. The abnormal RNA contained a transcript of the partially deleted polymerase gene covalently linked to the 3' end of the glycoprotein message. The polyadenylate is located at the 3' end of the molecule and is most probably encoded by the remnant polymerase gene polyadenylation signal. This aberrant RNA may be synthesized because of either a failure to terminate transcription at the end of the glycoprotein gene or an inability to process an abnormal polycistronic precursor.
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