Vaccinia virus has a genome of 185,000 bp that encodes approximately 200 polypeptides. These genes are expressed in a coordinated fashion so that some polypeptides are made before and others after DNA replication. In order to learn more about regulation of late gene expression, we sequenced an 8,600 base pair region of the vaccinia genome. Seven complete open-reading-frames were found. Six transcripts that initiated within this region were detected and of these four were synthesized only at late times. In each case, the transcriptional and translational start sites mapped within a few nucleotides of each other and the sequence TAAATG occurred at the start of the open-reading-frame. The putative promoter region of one late gene was analyzed by linking DNA segments to the coding region of the prokaryotic enzyme chloramphenicol acetyltransferase and recombining this construct into the vaccinia virus genome. By repeating this procedure with smaller and smaller putative promoter segments and assaying for enzyme activity, the location of the regulatory signals was determined. A rapidly sedimenting complex that accurately initiates and terminates transcription of early genes was isolated from vaccinia virus particles. Both a DNA-dependent ATPase and capping enzyme were associated with the transcription complex.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Intramural Research (Z01)
Project #
1Z01AI000307-05
Application #
3960535
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
5
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Niaid Extramural Activities
Department
Type
DUNS #
City
State
Country
United States
Zip Code
De Silva, Frank S; Paran, Nir; Moss, Bernard (2009) Products and substrate/template usage of vaccinia virus DNA primase. Virology 383:136-41
Katsafanas, George C; Moss, Bernard (2007) Colocalization of transcription and translation within cytoplasmic poxvirus factories coordinates viral expression and subjugates host functions. Cell Host Microbe 2:221-8
Parrish, Susan; Moss, Bernard (2007) Characterization of a second vaccinia virus mRNA-decapping enzyme conserved in poxviruses. J Virol 81:12973-8
Hebben, Matthias; Brants, Jan; Birck, Catherine et al. (2007) High level protein expression in mammalian cells using a safe viral vector: modified vaccinia virus Ankara. Protein Expr Purif 56:269-78
Parrish, Susan; Resch, Wolfgang; Moss, Bernard (2007) Vaccinia virus D10 protein has mRNA decapping activity, providing a mechanism for control of host and viral gene expression. Proc Natl Acad Sci U S A 104:2139-44
Garcia, Alonzo D; Otero, Joel; Lebowitz, Jacob et al. (2006) Quaternary structure and cleavage specificity of a poxvirus holliday junction resolvase. J Biol Chem 281:11618-26
Parrish, Susan; Moss, Bernard (2006) Characterization of a vaccinia virus mutant with a deletion of the D10R gene encoding a putative negative regulator of gene expression. J Virol 80:553-61
Domi, Arban; Moss, Bernard (2005) Engineering of a vaccinia virus bacterial artificial chromosome in Escherichia coli by bacteriophage lambda-based recombination. Nat Methods 2:95-7
De Silva, Frank S; Moss, Bernard (2005) Origin-independent plasmid replication occurs in vaccinia virus cytoplasmic factories and requires all five known poxvirus replication factors. Virol J 2:23
Katsafanas, George C; Moss, Bernard (2004) Vaccinia virus intermediate stage transcription is complemented by Ras-GTPase-activating protein SH3 domain-binding protein (G3BP) and cytoplasmic activation/proliferation-associated protein (p137) individually or as a heterodimer. J Biol Chem 279:52210-7

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