Abstract
The relative initiation rates for encephalomyocarditis virus mRNA and host mRNA's in infected cells were measured using two independent techniques. In both cases the results showed that viral mRNA initiates at a much higher rate than host mRNA'S. This difference was observed midway in the infectious cycle, well before virus-induced cytopathic effects (leakage of low-molecular-weight metabolites, failure to exclude trypan blue) were apparent. These results confirm that encephalomyocarditis viral mRNA is a more efficient initiator than host mRNA's in vivo, as has previously been demonstrated in in vitro experiments.
MeSH Terms
Animals
Anisomycin/pharmacology
Carcinoma, Krebs 2
Culture Techniques
Cycloheximide/pharmacology
Emetine/pharmacology
Encephalomyocarditis virus/metabolism
Molecular Weight
Neoplasm Proteins/biosynthesis
Peptide Biosynthesis
Peptide Chain Elongation, Translational/drug effects
Peptide Chain Initiation, Translational
RNA, Messenger/metabolism
RNA, Neoplasm/metabolism
RNA, Viral/metabolism
Viral Proteins/biosynthesis
Chemicals
Neoplasm Proteins
RNA, Messenger
RNA, Neoplasm
RNA, Viral
Viral Proteins
Anisomycin
Cycloheximide
Emetine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Jen G
Birge C H
Thach R E
References (23)
23 references, click to expand
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