Comparative Sequence Analysis of the Long Repeat Regions and Adjoining Parts of the Long Unique Regions in the Genomes of Herpes Simplex Viruses Types 1 and 2

MRC Virology Unit, Institute of Virology, University of Glasgow, Church Street, Glasgow G11 5JR, U.K. We report the determination of the DNA sequence of the long repeat (R L ) region and adjacent parts of the long unique (U L ) region in the genome of herpes simplex virus type 2 (HSV-2) strain HG52....

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Veröffentlicht in:Journal of general virology 1991-12, Vol.72 (12), p.3057-3075
Hauptverfasser: McGeoch, Duncan J, Cunningham, Charles, McIntyre, Graham, Dolan, Aidan
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creator McGeoch, Duncan J
Cunningham, Charles
McIntyre, Graham
Dolan, Aidan
description MRC Virology Unit, Institute of Virology, University of Glasgow, Church Street, Glasgow G11 5JR, U.K. We report the determination of the DNA sequence of the long repeat (R L ) region and adjacent parts of the long unique (U L ) region in the genome of herpes simplex virus type 2 (HSV-2) strain HG52. The DNA sequences and genetic content of the extremities of HSV-2 U L were found to be closely similar to those determined previously for HSV-1. The 5658 bp sequenced at the left end of HSV-2 U L contained coding regions for genes UL1 to UL4 plus part of UL5. The 4355 bp sequenced at the right end of U L contained coding regions for part of gene UL53, and the whole of genes UL54 to UL56. Comparison of the HSV-1 and HSV-2 UL56 sequences led to a correction in the published HSV-1 UL56 reading frame. The HSV-2 R L region, including one copy of the a sequence, was determined to be 9263 bp, with a base composition of 75.4% G+C and with many repetitive sequence elements. In HSV-2 R L , sequences were identified corresponding to HSV-1 genes encoding the immediate early IE110 (ICP0) transcriptional regulator and the ICP34.5 neurovirulence factor; the former HSV-2 gene was proposed to contain two introns, and the latter one intron. Downstream of the HSV-2 immediate early gene, the R L sequence encoding the latency-associated transcripts (LATs) was found to be dissimilar to that in HSV-1; the probable LAT promoter regions, however, showed similarities to HSV-1. Properties of the LAT sequences in both HSV-1 and HSV-2 were consistent with LATs being generated as an intron excised from a longer transcript. Received 12 June 1991; accepted 13 August 1991.
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The DNA sequences and genetic content of the extremities of HSV-2 U L were found to be closely similar to those determined previously for HSV-1. The 5658 bp sequenced at the left end of HSV-2 U L contained coding regions for genes UL1 to UL4 plus part of UL5. The 4355 bp sequenced at the right end of U L contained coding regions for part of gene UL53, and the whole of genes UL54 to UL56. Comparison of the HSV-1 and HSV-2 UL56 sequences led to a correction in the published HSV-1 UL56 reading frame. The HSV-2 R L region, including one copy of the a sequence, was determined to be 9263 bp, with a base composition of 75.4% G+C and with many repetitive sequence elements. In HSV-2 R L , sequences were identified corresponding to HSV-1 genes encoding the immediate early IE110 (ICP0) transcriptional regulator and the ICP34.5 neurovirulence factor; the former HSV-2 gene was proposed to contain two introns, and the latter one intron. 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The DNA sequences and genetic content of the extremities of HSV-2 U L were found to be closely similar to those determined previously for HSV-1. The 5658 bp sequenced at the left end of HSV-2 U L contained coding regions for genes UL1 to UL4 plus part of UL5. The 4355 bp sequenced at the right end of U L contained coding regions for part of gene UL53, and the whole of genes UL54 to UL56. Comparison of the HSV-1 and HSV-2 UL56 sequences led to a correction in the published HSV-1 UL56 reading frame. The HSV-2 R L region, including one copy of the a sequence, was determined to be 9263 bp, with a base composition of 75.4% G+C and with many repetitive sequence elements. In HSV-2 R L , sequences were identified corresponding to HSV-1 genes encoding the immediate early IE110 (ICP0) transcriptional regulator and the ICP34.5 neurovirulence factor; the former HSV-2 gene was proposed to contain two introns, and the latter one intron. 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Psychology</topic><topic>Genes, Viral</topic><topic>Genetics</topic><topic>herpes simplex virus 1</topic><topic>herpes simplex virus 2</topic><topic>Immediate-Early Proteins - genetics</topic><topic>Microbiology</topic><topic>Molecular Sequence Data</topic><topic>Repetitive Sequences, Nucleic Acid</topic><topic>RNA Splicing</topic><topic>Sequence Alignment</topic><topic>Simplexvirus - genetics</topic><topic>Transcription, Genetic</topic><topic>Ubiquitin-Protein Ligases</topic><topic>Viral Proteins</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>McGeoch, Duncan J</creatorcontrib><creatorcontrib>Cunningham, Charles</creatorcontrib><creatorcontrib>McIntyre, Graham</creatorcontrib><creatorcontrib>Dolan, Aidan</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>McGeoch, Duncan J</au><au>Cunningham, Charles</au><au>McIntyre, Graham</au><au>Dolan, Aidan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative Sequence Analysis of the Long Repeat Regions and Adjoining Parts of the Long Unique Regions in the Genomes of Herpes Simplex Viruses Types 1 and 2</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>1991-12</date><risdate>1991</risdate><volume>72</volume><issue>12</issue><spage>3057</spage><epage>3075</epage><pages>3057-3075</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><coden>JGVIAY</coden><abstract>MRC Virology Unit, Institute of Virology, University of Glasgow, Church Street, Glasgow G11 5JR, U.K. We report the determination of the DNA sequence of the long repeat (R L ) region and adjacent parts of the long unique (U L ) region in the genome of herpes simplex virus type 2 (HSV-2) strain HG52. The DNA sequences and genetic content of the extremities of HSV-2 U L were found to be closely similar to those determined previously for HSV-1. The 5658 bp sequenced at the left end of HSV-2 U L contained coding regions for genes UL1 to UL4 plus part of UL5. The 4355 bp sequenced at the right end of U L contained coding regions for part of gene UL53, and the whole of genes UL54 to UL56. Comparison of the HSV-1 and HSV-2 UL56 sequences led to a correction in the published HSV-1 UL56 reading frame. The HSV-2 R L region, including one copy of the a sequence, was determined to be 9263 bp, with a base composition of 75.4% G+C and with many repetitive sequence elements. In HSV-2 R L , sequences were identified corresponding to HSV-1 genes encoding the immediate early IE110 (ICP0) transcriptional regulator and the ICP34.5 neurovirulence factor; the former HSV-2 gene was proposed to contain two introns, and the latter one intron. 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subjects Amino Acid Sequence
Base Sequence
Biological and medical sciences
DNA, Viral - genetics
Fundamental and applied biological sciences. Psychology
Genes, Viral
Genetics
herpes simplex virus 1
herpes simplex virus 2
Immediate-Early Proteins - genetics
Microbiology
Molecular Sequence Data
Repetitive Sequences, Nucleic Acid
RNA Splicing
Sequence Alignment
Simplexvirus - genetics
Transcription, Genetic
Ubiquitin-Protein Ligases
Viral Proteins
Virology
title Comparative Sequence Analysis of the Long Repeat Regions and Adjoining Parts of the Long Unique Regions in the Genomes of Herpes Simplex Viruses Types 1 and 2
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