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AbstractAbstract
[en] The transcriptional organization of the genome of herpes simplex virus type 1 was analyzed by measuring the sensitivity of viral polypeptide synthesis to uv irradiation of the infecting virus. Herpes simplex virus type 1 was irradiated with various doses of uv light and used to infect xeroderma pigmentosum fibroblasts. Immediate early transcription units were analyzed by having cycloheximide present throughout the period of infection, removing the drug at 8 h postinfection, and pulse-labeling proteins with [355]methionine. Delayed early transcription units were analyzed in similar studies by having 9-beta-D-arabinofuranosyladenine present during the experiment to block replication of the input irradiated genome. The results indicate that none of the immediate early genes analyzed can be cotranscribed, whereas some of the delayed early genes might be cotranscribed. No evidence was found for the existence of large, multigene transcription units
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Journal Article
Journal
Journal of Virology; ISSN 0022-538X;
; v. 34(3); p. 604-614

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AMINES, AMINO ACIDS, ANIMAL CELLS, ANTIBIOTICS, BETA DECAY RADIOISOTOPES, BETA-MINUS DECAY RADIOISOTOPES, BIOLOGICAL EFFECTS, CARBOXYLIC ACIDS, DAYS LIVING RADIOISOTOPES, DISEASES, DRUGS, ELECTROMAGNETIC RADIATION, EVEN-ODD NUCLEI, FUNGICIDES, HETEROCYCLIC COMPOUNDS, INFECTIOUS DISEASES, ISOTOPES, LIGHT NUCLEI, LIPOTROPIC FACTORS, NUCLEI, NUCLEIC ACIDS, ORGANIC ACIDS, ORGANIC COMPOUNDS, ORGANIC NITROGEN COMPOUNDS, ORGANIC SULFUR COMPOUNDS, PEPTIDES, PESTICIDES, PROTEINS, PURINES, RADIATION EFFECTS, RADIATIONS, RADIOISOTOPES, RNA, SKIN DISEASES, SULFUR ISOTOPES, SYNTHESIS
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