DNA Sequence Anaylysis of an Immediate-Early Gene Region of the Herpes Simplex Virus Type 1 Genome (Map Coordinates 0.950 to 0.978)
- 1 September 1982
- journal article
- research article
- Published by Microbiology Society in Journal of General Virology
- Vol. 62 (1) , 1-15
- https://doi.org/10.1099/0022-1317-62-1-1
Abstract
The nucleotide sequence of 4 kilobases of DNA from within the short region of the genome of herpes simplex virus type 1 was determined. This portion of DNA contains the junctions of the terminal and internal inverted repeat sequence components, with the unique sequence component and the 5'' regions of the genes which encode the Vmw 12, Vmw 68 and Vmw 175 immediate-early polypeptides. The transcription and translation initiation sites of all 3 genes and the 5'' and 3'' boundaries of the Vmw 12 and Vmw 68 gene introns have been localized on the DNA sequence and shown to be flanked by sequences which resemble those found in similar positions in other eukaryotic genes. For the Vmw 12 and Vmw 68 genes the promoters, the 5''-non-coding regions of the mRNA, and the introns lie within the terminal and internal inverted repeats, respectively, while the polypeptide-coding regions lie in the short unique component. The introns consist largely of tandemly reiterated copies of a 22-nucleotide sequence: the Vmw 12 gene intron contains 7 of these and the Vmw 68 gene intron 5. The Vmw 175 gene is located entirely within the short repeats, of which those regions sequenced here have extremely high G + C content of 78%, in marked contrast to the value of 66% obtained for the adjacent region of the unique sequence component. Prediction of the complete amino acid sequence of the Vmw 12 polypeptide, accounting for a MW of 9830, and of the first 523 amino-terminal amino acids of the Vmw 175 polypeptide has been made from the DNA sequence. The polypeptide-coding region of the Vmw 175 gene has an average G + C content of 80% but nevertheless specifies a wide range of amino acid types because of the maximal assignment of G and C residues to codon third base positions.This publication has 24 references indexed in Scilit:
- Recombinants between herpes simplex virus types 1 and 2: analyses of genome structures and expression of immediate early polypeptidesJournal of Virology, 1978
- Temperature-sensitive mutants of herpes simplex virus type 1 defective in transcriptional and post-transcriptional functions required for viral DNA synthesisVirology, 1978
- The Genome of Simian Virus 40Science, 1978
- Anatomy of herpes simplex virus (HSV) DNA. X. Mapping of viral genes by analysis of polypeptides and functions specified by HSV-1 X HSV-2 recombinantsJournal of Virology, 1978
- Spliced early mRNAs of simian virus 40Proceedings of the National Academy of Sciences, 1978
- A new method for sequencing DNA.Proceedings of the National Academy of Sciences, 1977
- Temporal regulation of herpes simplex virus type 1 transcription: location of transcripts on the viral genomePublished by Elsevier ,1977
- Sequence arrangement in herpes simplex virus type 1 DNA: identification of terminal fragments in restriction endonuclease digests and evidence for inversions in redundant and unique sequencesJournal of Virology, 1976
- Physical maps for Herpes simplex virus type 1 DNA for restriction endonucleases Hind III, Hpa-1, and X. badJournal of Virology, 1976
- In vivo methylation by Escherichia coli K-12 mec+ deoxyribonucleic acid-cytosine methylase protects against in vitro cleavage by the RII restriction endonuclease (R. Eco RII)Journal of Bacteriology, 1976