Sequence of the Putative Origin of Replication in the UL Region of Herpes Simplex Virus Type 1 ANG DNA

Institute for Virus Research, German Cancer Research Center, 6900 Heidelberg, Federal Republic of Germany Interest has been stimulated concerning the region mapping between 0.38 and 0.42 on the prototype configuration of the herpes simplex virus type 1 (HSV-1) genome due to the high probability of t...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of general virology 1984-12, Vol.65 (12), p.2109-2119
Hauptverfasser: Gray, C. P, Kaerner, H. C
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2119
container_issue 12
container_start_page 2109
container_title Journal of general virology
container_volume 65
creator Gray, C. P
Kaerner, H. C
description Institute for Virus Research, German Cancer Research Center, 6900 Heidelberg, Federal Republic of Germany Interest has been stimulated concerning the region mapping between 0.38 and 0.42 on the prototype configuration of the herpes simplex virus type 1 (HSV-1) genome due to the high probability of the presence there of a second origin of DNA replication. A 960 bp restriction fragment ( Hin fI E) of a class II defective HSV-1 ANG DNA has been sequenced using the viral DNA rather than molecularly cloned DNA. This fragment includes the Bam HI U/R cleavage site, mapping at approximately 0.4. Part of the sequence derived in this study displays homology with the origins of DNA replication contained in TR S /IR S of HSV-1 and HSV-2 DNA. The homologous region comprising 76 bp occurs as two copies, each of which contains two palindromically arranged copies of an 8 bp sequence identical to the ‘consensus’ sequence reported to be part of the origin of DNA replication at the terminus of the mammalian adenoviruses. It can be deduced from a comparison of this structure to the TR S /IR S origin of HSV-1 and HSV-2 that there are two origins of replication in the U L region of HSV-1 ANG DNA. Assuming that the orientation of the consensus sequence is relevant to the direction of DNA replication, one can conclude that the U L origin(s) of HSV-1 ANG is (are) bidirectional. It has not yet been possible to clone DNA fragments molecularly which include the region spanning the U L origin(s) of HSV-1 DNA. Keywords: HSV-1, U L , origin of replication Present address: EMBL, Meyerhofstrasse 1, 6900 Heidelberg, F.R.G. Received 5 June 1984; accepted 29 August 1984.
doi_str_mv 10.1099/0022-1317-65-12-2109
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_75823260</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>75823260</sourcerecordid><originalsourceid>FETCH-LOGICAL-c343t-e5fc92ede2769b6a7197739370bced408cf5eb00a6bd369475ed8b8f5d80cccb3</originalsourceid><addsrcrecordid>eNpNkE1P3DAQhi0EolvKPwDJB4TUQ4o_Yjs-roBCpRVUBXq1HGey6ypf2AmUf19Hu1r1ZPmZZ2bsF6EzSr5RovUVIYxllFOVSZFRlrFED9CC5unKknCIFnvlE_oc4x9CaJ4LdYyOJdEyL_QC1U_wOkHnAPc1HjeAf06jHf0b4Mfg176b8S8YGu8S7TucyGy9rBJdzyDV7yEMEPGTb4cG_uLfPkwRP38MgClePtzhm4flF3RU2ybC6e48QS_fb5-v77PV492P6-UqczznYwaidppBBUxJXUqrqFaKa65I6aDKSeFqASUhVpYVlzpXAqqiLGpRFcQ5V_ITdLmdO4Q-_SuOpvXRQdPYDvopGiUKxpkkScy3ogt9jAFqMwTf2vBhKDFzvGbOzszZGSkMZWaON7Wd7-ZPZQvVvmmXZ6pf7Oo2OtvUwXbOx72mKeFSzNrXrbbx6827D2DW0LU-vaX0vXnz4b-V_wD1jY90</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>75823260</pqid></control><display><type>article</type><title>Sequence of the Putative Origin of Replication in the UL Region of Herpes Simplex Virus Type 1 ANG DNA</title><source>MEDLINE</source><source>Microbiology Society</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><source>Alma/SFX Local Collection</source><creator>Gray, C. P ; Kaerner, H. C</creator><creatorcontrib>Gray, C. P ; Kaerner, H. C</creatorcontrib><description>Institute for Virus Research, German Cancer Research Center, 6900 Heidelberg, Federal Republic of Germany Interest has been stimulated concerning the region mapping between 0.38 and 0.42 on the prototype configuration of the herpes simplex virus type 1 (HSV-1) genome due to the high probability of the presence there of a second origin of DNA replication. A 960 bp restriction fragment ( Hin fI E) of a class II defective HSV-1 ANG DNA has been sequenced using the viral DNA rather than molecularly cloned DNA. This fragment includes the Bam HI U/R cleavage site, mapping at approximately 0.4. Part of the sequence derived in this study displays homology with the origins of DNA replication contained in TR S /IR S of HSV-1 and HSV-2 DNA. The homologous region comprising 76 bp occurs as two copies, each of which contains two palindromically arranged copies of an 8 bp sequence identical to the ‘consensus’ sequence reported to be part of the origin of DNA replication at the terminus of the mammalian adenoviruses. It can be deduced from a comparison of this structure to the TR S /IR S origin of HSV-1 and HSV-2 that there are two origins of replication in the U L region of HSV-1 ANG DNA. Assuming that the orientation of the consensus sequence is relevant to the direction of DNA replication, one can conclude that the U L origin(s) of HSV-1 ANG is (are) bidirectional. It has not yet been possible to clone DNA fragments molecularly which include the region spanning the U L origin(s) of HSV-1 DNA. Keywords: HSV-1, U L , origin of replication Present address: EMBL, Meyerhofstrasse 1, 6900 Heidelberg, F.R.G. Received 5 June 1984; accepted 29 August 1984.</description><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/0022-1317-65-12-2109</identifier><identifier>PMID: 6096489</identifier><identifier>CODEN: JGVIAY</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>Base Sequence ; Biological and medical sciences ; Chromosome Deletion ; Cloning, Molecular ; Defective Viruses - genetics ; DNA Replication ; DNA, Viral - genetics ; Escherichia coli - genetics ; Fundamental and applied biological sciences. Psychology ; Genes, Regulator ; Genes, Viral ; Microbiology ; Morphology, structure, chemical composition, physicochemical properties ; Simplexvirus - genetics ; Virology</subject><ispartof>Journal of general virology, 1984-12, Vol.65 (12), p.2109-2119</ispartof><rights>1985 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c343t-e5fc92ede2769b6a7197739370bced408cf5eb00a6bd369475ed8b8f5d80cccb3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,3733,3734,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=9103659$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/6096489$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gray, C. P</creatorcontrib><creatorcontrib>Kaerner, H. C</creatorcontrib><title>Sequence of the Putative Origin of Replication in the UL Region of Herpes Simplex Virus Type 1 ANG DNA</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>Institute for Virus Research, German Cancer Research Center, 6900 Heidelberg, Federal Republic of Germany Interest has been stimulated concerning the region mapping between 0.38 and 0.42 on the prototype configuration of the herpes simplex virus type 1 (HSV-1) genome due to the high probability of the presence there of a second origin of DNA replication. A 960 bp restriction fragment ( Hin fI E) of a class II defective HSV-1 ANG DNA has been sequenced using the viral DNA rather than molecularly cloned DNA. This fragment includes the Bam HI U/R cleavage site, mapping at approximately 0.4. Part of the sequence derived in this study displays homology with the origins of DNA replication contained in TR S /IR S of HSV-1 and HSV-2 DNA. The homologous region comprising 76 bp occurs as two copies, each of which contains two palindromically arranged copies of an 8 bp sequence identical to the ‘consensus’ sequence reported to be part of the origin of DNA replication at the terminus of the mammalian adenoviruses. It can be deduced from a comparison of this structure to the TR S /IR S origin of HSV-1 and HSV-2 that there are two origins of replication in the U L region of HSV-1 ANG DNA. Assuming that the orientation of the consensus sequence is relevant to the direction of DNA replication, one can conclude that the U L origin(s) of HSV-1 ANG is (are) bidirectional. It has not yet been possible to clone DNA fragments molecularly which include the region spanning the U L origin(s) of HSV-1 DNA. Keywords: HSV-1, U L , origin of replication Present address: EMBL, Meyerhofstrasse 1, 6900 Heidelberg, F.R.G. Received 5 June 1984; accepted 29 August 1984.</description><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>Chromosome Deletion</subject><subject>Cloning, Molecular</subject><subject>Defective Viruses - genetics</subject><subject>DNA Replication</subject><subject>DNA, Viral - genetics</subject><subject>Escherichia coli - genetics</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Regulator</subject><subject>Genes, Viral</subject><subject>Microbiology</subject><subject>Morphology, structure, chemical composition, physicochemical properties</subject><subject>Simplexvirus - genetics</subject><subject>Virology</subject><issn>0022-1317</issn><issn>1465-2099</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNkE1P3DAQhi0EolvKPwDJB4TUQ4o_Yjs-roBCpRVUBXq1HGey6ypf2AmUf19Hu1r1ZPmZZ2bsF6EzSr5RovUVIYxllFOVSZFRlrFED9CC5unKknCIFnvlE_oc4x9CaJ4LdYyOJdEyL_QC1U_wOkHnAPc1HjeAf06jHf0b4Mfg176b8S8YGu8S7TucyGy9rBJdzyDV7yEMEPGTb4cG_uLfPkwRP38MgClePtzhm4flF3RU2ybC6e48QS_fb5-v77PV492P6-UqczznYwaidppBBUxJXUqrqFaKa65I6aDKSeFqASUhVpYVlzpXAqqiLGpRFcQ5V_ITdLmdO4Q-_SuOpvXRQdPYDvopGiUKxpkkScy3ogt9jAFqMwTf2vBhKDFzvGbOzszZGSkMZWaON7Wd7-ZPZQvVvmmXZ6pf7Oo2OtvUwXbOx72mKeFSzNrXrbbx6827D2DW0LU-vaX0vXnz4b-V_wD1jY90</recordid><startdate>198412</startdate><enddate>198412</enddate><creator>Gray, C. P</creator><creator>Kaerner, H. C</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>7X8</scope></search><sort><creationdate>198412</creationdate><title>Sequence of the Putative Origin of Replication in the UL Region of Herpes Simplex Virus Type 1 ANG DNA</title><author>Gray, C. P ; Kaerner, H. C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c343t-e5fc92ede2769b6a7197739370bced408cf5eb00a6bd369475ed8b8f5d80cccb3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>Chromosome Deletion</topic><topic>Cloning, Molecular</topic><topic>Defective Viruses - genetics</topic><topic>DNA Replication</topic><topic>DNA, Viral - genetics</topic><topic>Escherichia coli - genetics</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes, Regulator</topic><topic>Genes, Viral</topic><topic>Microbiology</topic><topic>Morphology, structure, chemical composition, physicochemical properties</topic><topic>Simplexvirus - genetics</topic><topic>Virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gray, C. P</creatorcontrib><creatorcontrib>Kaerner, H. C</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>MEDLINE - Academic</collection><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gray, C. P</au><au>Kaerner, H. C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sequence of the Putative Origin of Replication in the UL Region of Herpes Simplex Virus Type 1 ANG DNA</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>1984-12</date><risdate>1984</risdate><volume>65</volume><issue>12</issue><spage>2109</spage><epage>2119</epage><pages>2109-2119</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><coden>JGVIAY</coden><abstract>Institute for Virus Research, German Cancer Research Center, 6900 Heidelberg, Federal Republic of Germany Interest has been stimulated concerning the region mapping between 0.38 and 0.42 on the prototype configuration of the herpes simplex virus type 1 (HSV-1) genome due to the high probability of the presence there of a second origin of DNA replication. A 960 bp restriction fragment ( Hin fI E) of a class II defective HSV-1 ANG DNA has been sequenced using the viral DNA rather than molecularly cloned DNA. This fragment includes the Bam HI U/R cleavage site, mapping at approximately 0.4. Part of the sequence derived in this study displays homology with the origins of DNA replication contained in TR S /IR S of HSV-1 and HSV-2 DNA. The homologous region comprising 76 bp occurs as two copies, each of which contains two palindromically arranged copies of an 8 bp sequence identical to the ‘consensus’ sequence reported to be part of the origin of DNA replication at the terminus of the mammalian adenoviruses. It can be deduced from a comparison of this structure to the TR S /IR S origin of HSV-1 and HSV-2 that there are two origins of replication in the U L region of HSV-1 ANG DNA. Assuming that the orientation of the consensus sequence is relevant to the direction of DNA replication, one can conclude that the U L origin(s) of HSV-1 ANG is (are) bidirectional. It has not yet been possible to clone DNA fragments molecularly which include the region spanning the U L origin(s) of HSV-1 DNA. Keywords: HSV-1, U L , origin of replication Present address: EMBL, Meyerhofstrasse 1, 6900 Heidelberg, F.R.G. Received 5 June 1984; accepted 29 August 1984.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>6096489</pmid><doi>10.1099/0022-1317-65-12-2109</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0022-1317
ispartof Journal of general virology, 1984-12, Vol.65 (12), p.2109-2119
issn 0022-1317
1465-2099
language eng
recordid cdi_proquest_miscellaneous_75823260
source MEDLINE; Microbiology Society; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Base Sequence
Biological and medical sciences
Chromosome Deletion
Cloning, Molecular
Defective Viruses - genetics
DNA Replication
DNA, Viral - genetics
Escherichia coli - genetics
Fundamental and applied biological sciences. Psychology
Genes, Regulator
Genes, Viral
Microbiology
Morphology, structure, chemical composition, physicochemical properties
Simplexvirus - genetics
Virology
title Sequence of the Putative Origin of Replication in the UL Region of Herpes Simplex Virus Type 1 ANG DNA
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-30T06%3A53%3A34IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sequence%20of%20the%20Putative%20Origin%20of%20Replication%20in%20the%20UL%20Region%20of%20Herpes%20Simplex%20Virus%20Type%201%20ANG%20DNA&rft.jtitle=Journal%20of%20general%20virology&rft.au=Gray,%20C.%20P&rft.date=1984-12&rft.volume=65&rft.issue=12&rft.spage=2109&rft.epage=2119&rft.pages=2109-2119&rft.issn=0022-1317&rft.eissn=1465-2099&rft.coden=JGVIAY&rft_id=info:doi/10.1099/0022-1317-65-12-2109&rft_dat=%3Cproquest_cross%3E75823260%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=75823260&rft_id=info:pmid/6096489&rfr_iscdi=true