Abstract
BHK cells infected with defective-interfering passages of Sindbis virus accumulate a species of RNA (20S) that is about half the molecular weight of the major viral mRNA (26S). We have performed competitive hybridization experiments with these species of RNA and have established that 20S RNA contains approximately 50% of the nucleotide sequences present in 26S RNA. Our further studies, however, demonstrate that 20S RNA is unable to carry out the messenger function of 26S RNA. We found very little of the defective RNA associated with polysomes in vivo. In addition, it was unable to stimulate protein synthesis in vitro under conditions in which 26S RNA was translated. We have also examined viral RNA synthesis in BHK cells infected with standard or defective-interfering passages of Sindbis virus. This comparison suggests that defective partioles do not synthesize a functional replicase.
MeSH Terms
Animals
Base Sequence
Cell Line
Cell-Free System
Cricetinae
Defective Viruses/analysis,growth & development,metabolism
Electrophoresis, Polyacrylamide Gel
Kidney
Nucleic Acid Hybridization
Phosphorus Radioisotopes
Polyribosomes/metabolism
Protein Biosynthesis
RNA, Messenger
RNA, Viral/analysis,biosynthesis
Sindbis Virus/analysis,growth & development,metabolism
Sulfur Radioisotopes
Tritium
Uridine/metabolism
Viral Interference
Viral Proteins/biosynthesis
Virus Replication
Chemicals
Phosphorus Radioisotopes
RNA, Messenger
RNA, Viral
Sulfur Radioisotopes
Viral Proteins
Tritium
Uridine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Weiss B
Goran D
Cancedda R
Schlesinger S
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