Abstract
The small defective T particle of vesicular stomatitis virus (VSV-111) has no detectable enzyme activity when assayed at 31 C, although qualitatively it possesses all the virion proteins found in complete VSV-1 virions. With VSV-1 transcription product ribonucleic acid (RNA), it is shown that the VSV-111 RNA is identical to part of the VSV-1 genome. Evidence is also presented to support the idea that in vitro VSV-1 transcription is sequential.
MeSH Terms
Animals
Cell Line
Centrifugation, Density Gradient
Cricetinae
Defective Viruses/analysis,enzymology,metabolism
Electrophoresis, Disc
Genetic Code
Genetics, Microbial
Kidney
Phosphorus Isotopes
RNA Nucleotidyltransferases/metabolism
RNA, Viral/analysis,biosynthesis
Ribonucleases
Tritium
Uracil Nucleotides/metabolism
Uridine/metabolism
Vesicular stomatitis Indiana virus/analysis,enzymology,isolation & purification,metabolism
Viral Interference
Virus Cultivation
Chemicals
Phosphorus Isotopes
RNA, Viral
Uracil Nucleotides
Tritium
RNA Nucleotidyltransferases
Ribonucleases
Uridine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Roy P
Bishop D H
References (20)
20 references, click to expand
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