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 |
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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. |
doi_str_mv | 10.1099/0022-1317-72-12-3057 |
format | Article |
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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;
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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.</description><subject>Amino Acid Sequence</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>DNA, Viral - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Viral</subject><subject>Genetics</subject><subject>herpes simplex virus 1</subject><subject>herpes simplex virus 2</subject><subject>Immediate-Early Proteins - genetics</subject><subject>Microbiology</subject><subject>Molecular Sequence Data</subject><subject>Repetitive Sequences, Nucleic Acid</subject><subject>RNA Splicing</subject><subject>Sequence Alignment</subject><subject>Simplexvirus - genetics</subject><subject>Transcription, Genetic</subject><subject>Ubiquitin-Protein Ligases</subject><subject>Viral Proteins</subject><subject>Virology</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1991</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc-O0zAQxi0EWsrCG4DkA0LiEPCf2G6OVQW7SJVA7C5Xa5pMWq8SO9jpQl-GZ8VpqwInTuPx95vPI3-EvOTsHWdV9Z4xIQouuSlMrqKQTJlHZMZLrQqRgcdkdkaekmcp3TPGy1KZC3LBtRa6MjPyaxn6ASKM7gHpDX7foa-RLjx0--QSDS0dt0hXwW_oVxwQxlw2LvhEwTd00dwH510Wv0Ac_8XvvMtuZ9z5g3SFPvR4IK8xDvl04_qhw5_0m4u7lPvb_XTLD_7iOXnSQpfwxalekruPH26X18Xq89Wn5WJV1KWQptB6Dkw2oFvQHBg3IEHjmrFm-giYr2vM_VyqqpIGlBGiqqqmNai15FWt5CV5c_QdYshbp9H2LtXYdeAx7JI1Io8qJf8Lci2kZlJksDyCdQwpRWztEF0PcW85s1N-dgrHTuFkd8uFnfLLY69O_rt1j82foWNgWX990iHV0LURfO3SGVNcsJLpjL09Ylu32f5wEe0Gfe_yLmsX7IOLfz35GyzHsJI</recordid><startdate>199112</startdate><enddate>199112</enddate><creator>McGeoch, Duncan J</creator><creator>Cunningham, Charles</creator><creator>McIntyre, Graham</creator><creator>Dolan, Aidan</creator><general>Soc General Microbiol</general><general>Society for General Microbiology</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7U9</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>199112</creationdate><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</title><author>McGeoch, Duncan J ; Cunningham, Charles ; McIntyre, Graham ; Dolan, Aidan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4237-668a03da6fa61a017a3a6eb00d2099a8bcea6e8359937a5722999df7e66319c53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Amino Acid Sequence</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>DNA, Viral - genetics</topic><topic>Fundamental and applied biological sciences. 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. 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.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>1662697</pmid><doi>10.1099/0022-1317-72-12-3057</doi><tpages>19</tpages><oa>free_for_read</oa></addata></record> |
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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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