Abstract
Three noncomplementing vaccinia virus temperature-sensitive mutants, ts4, ts22, and ts23, exhibit an abortive late phenotype characterized by the simultaneous cessation of protein synthesis, the breakdown of rRNA and viral mRNA, and an increase in intracellular concentrations of 2'-5'-linked oligoadenylates late during infection at the nonpermissive temperature (R.F. Pacha and R.C. Condit, J. Virol. 56:395-403, 1985; R.J. Cohrs, R.C. Condit, R.F. Pacha, C.L. Thompson, and O.K. Sharma, J. Virol. 63:948-951, 1989). We have identified the virus gene affected by the abortive late mutants, determined its DNA sequence, and analyzed its transcription. The gene resides in the HindIII A DNA fragment, it has a predicted coding capacity of 57 kilodaltons, and it is transcribed both early and late during infection. The early transcript of the abortive late gene is unusual; it contains a 426-nucleotide 5' untranslated region, and it must be synthesized by transcription through an early transcription termination signal which is located in the middle of the gene in a hairpin loop structure. DNA sequence and transcription analysis of two flanking genes is also presented.
MeSH Terms
Amino Acid Sequence
Animals
Base Sequence
Blotting, Northern
Cell Line
Cell Transformation, Viral
Cloning, Molecular
Gene Expression
Genes, Viral
Molecular Sequence Data
Mutation
Nucleic Acid Conformation
Oligonucleotide Probes
Phenotype
Protein Biosynthesis
RNA, Messenger/genetics,metabolism
RNA, Ribosomal/genetics,metabolism
RNA, Viral/genetics,metabolism
Restriction Mapping
Vaccinia virus/genetics
Chemicals
Oligonucleotide Probes
RNA, Messenger
RNA, Ribosomal
RNA, Viral
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Pacha R F
Department of Biochemistry, State University of New York, Buffalo 14214.
Meis R J
Condit R C
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