The induction of interferon by natural and synthetic polynucleotides.hs.
Explore the source record for details and available documents.
Biomedical subjects
Publications and source records attributed to C Colby.
Explore the source record for details and available documents.
The synthesis of vaccinia virus double-stranded ribonucleic acid (RNA) in infected HeLa cells was sensitive to actinomycin D, suggesting that a deoxyribonucleic acid dependent reaction is involved. Some double-stranded RNA was made in the presence of cytosine arabinoside in infected cells. Double-stranded and complementary RNA were synthesized in vitro by using vaccinia cores. These two observations indicate that some of the double-stranded RNA is read from "early" genes. The double-stranded RNA synthesized in vitro had the same properties as that made in vivo. At least 70% of the double-stranded RNA made in vivo was in ribonuclease-resistant form prior to sodium dodecyl sulfate-phenol extraction. In addition, there was a complementary RNA in infected cells which could be converted to double-stranded RNA by annealing.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Treatment of chick embryo cells growing in culture with rI:rC and many other RNA-like polymers results in the induction of interferon. DEAE dextran is required to facilitate the uptake of the RNA into the cells. Interferon-inducing activity is found with a variety of double-stranded helical polynucleotides, provided that all the sugar residues are ribose. However, the effectiveness of different active polynucleotides at a given concentration varies considerably. The differences in activity among the various polynucleotides do not appear to reflect differences in the rate or amount of uptake into the cells or in the rate of intracellular breakdown. Thehigh degree of specificity of the induction process is consistent with the existence of a specific intracellular receptor site, which may be a protein.
The virus-specific, RNase-resistant RNA appearing in vaccinia virus-infected cells was directly shown to be an RNA duplex. After its melting and subsequent banding on Cs(2)SO(4) or incubation with DNase, the RNA could be reannealed and then hybridized with vaccinia virus DNA.The double-stranded virus-specific RNA appears to exist in the cell in the form of heterogeneous partially double-stranded RNA's sedimenting between 9 and 22S. The kinetics of the appearance of the double-stranded RNA in the cell show a dependence on the multiplicity of infection and suggest that the double-stranded RNA is a "late" product of viral intracellular biosynthesis. The synthesis of the double-stranded RNA is inhibited by actinomycin D.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.
Explore the source record for details and available documents.