Abstract
Small amounts of fractionated, denatured, (32)P-labeled DNA from SV40 virus were incubated with a large excess of the complementary RNA of SV40 prepared in vitro with Escherichia coli RNA polymerase; the viral DNA strands were separated on hydroxyapatite columns. The RNA present in green monkey cells late in the lytic cycle reacted with 40-42% of the strand complementary to the in vitro complementary RNA (minus strand), and 60-64% of the opposite (plus) strand. "Early lytic" RNA failed to significantly interact with the plus strand, but formed stable duplex molecules with 35-39% of the minus strand. The RNA prepared from mouse embryo cells 24 hr after infection with SV40 combined with 35-38% of the minus strand and 60-62% of the plus strand. In all cases, the same regions of either the plus or minus strand appear to be transcribed in permissive and nonpermissive infections.
MeSH Terms
Animals
Cell Line
Centrifugation, Density Gradient
Chromatography
Cytarabine/pharmacology
DNA, Viral/biosynthesis,isolation & purification
Embryo, Mammalian/metabolism
Escherichia coli/enzymology
Haplorhini
Hydroxyapatites
Kidney/drug effects,metabolism
Mice
Nucleic Acid Denaturation
Nucleic Acid Hybridization
Phosphates/metabolism
Phosphorus Isotopes
RNA Nucleotidyltransferases
RNA, Viral/biosynthesis
Simian virus 40
Templates, Genetic
Chemicals
DNA, Viral
Hydroxyapatites
Phosphates
Phosphorus Isotopes
RNA, Viral
Cytarabine
RNA Nucleotidyltransferases
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Khoury G
Byrne J C
Martin M A
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