Abstract |
Virion RNA from the avian leukosis virus Rous-associated virus 2 (RAV-2) and poly(A)-containing RNAs from RAV-2-infected chick embryo fibroblasts were microinjected into fibroblasts transformed by the Bryan high-titer strain of Rous sarcoma virus (RSV), which is deficient in viral envelope glycoprotein. Production of infectious RSV following these injections depended upon the viral envelope-messenger activity of the injected RNA. This system constituted a sensitive and rigorous assay system for viral envelope- messenger RNA. It was found that 21S mRNA from RAV-2-infected cells expressed the highest activity, while 35S mRNA expressed comparatively little. In addition, RAV-2-virion RNA expressed little messenger activity. The rate of formation of infectious RSV following 21S mRNA injections reached a peak near 9 hr, which was followed by a rapid decline. Evidence has been obtained that a small fraction of both 35S virion RNA and 35S mRNA from virus-infected cells was encapsulated into virus particles following their injection into virus-producing cells.
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Authors | D W Stacey, V G Allfrey, H Hanafusa |
Journal | Proceedings of the National Academy of Sciences of the United States of America
(Proc Natl Acad Sci U S A)
Vol. 74
Issue 4
Pg. 1614-8
(Apr 1977)
ISSN: 0027-8424 [Print] United States |
PMID | 193109
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Glycoproteins
- Membrane Proteins
- RNA, Messenger
- RNA, Viral
- Poly A
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Topics |
- Animals
- Avian Leukosis Virus
- Chick Embryo
- Fibroblasts
(metabolism)
- Glycoproteins
(biosynthesis)
- Kinetics
- Membrane Proteins
(biosynthesis)
- Microinjections
- Poly A
- Protein Biosynthesis
- RNA, Messenger
(metabolism)
- RNA, Viral
(metabolism)
- Virus Replication
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