Abstract
Vaccinia virus DNA polymerase, a single-subunit enzyme of 110,000 molecular weight, is induced early after infection. Genetic analysis suggests that the gene encoding the enzyme maps within a 15-kilobase HindIII fragment located 45 kilobases from the left-hand end of the genome. We identified the in vitro translation product with these properties and mapped the transcript by hybrid selection, RNA filter hybridization, and S1 nuclease mapping. Two mRNAs from this region, 3.4 and 3.9 kilobases in size, could be translated in vitro to yield a 110K polypeptide. The two RNAs shared a common 5' terminus and had staggered 3' ends. Sequences mapping entirely within this gene were shown to be biologically active in rescuing mutants with temperature-sensitive or drug-resistant polymerase activity to the wild-type phenotype.
MeSH Terms
Chromosome Mapping
DNA Restriction Enzymes
DNA-Directed DNA Polymerase/genetics
Endonucleases
Genes, Viral
Molecular Weight
RNA, Messenger/genetics
RNA, Viral/genetics
Single-Strand Specific DNA and RNA Endonucleases
Transcription, Genetic
Vaccinia virus/genetics
Chemicals
RNA, Messenger
RNA, Viral
DNA-Directed DNA Polymerase
Endonucleases
DNA Restriction Enzymes
Single-Strand Specific DNA and RNA Endonucleases
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Traktman P
Sridhar P
Condit R C
Roberts B E
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