Mapping sequences required for productive replication of beet necrotic yellow vein virus RNA 3

Of the four genome components of beet necrotic yellow vein virus only RNAs 1 and 2 are essential for viral replication in leaves. We have mapped cis-regulatory elements on RNA 3 by introducing deletions into expressible cDNA clones and inoculating leaves with the altered transcripts along with RNAs...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Virology (New York, N.Y.) N.Y.), 1990-09, Vol.178 (1), p.273-280
Hauptverfasser: Jupin, I., Richards, K., Jonard, G., Guilley, H., Pleij, C.W.A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 280
container_issue 1
container_start_page 273
container_title Virology (New York, N.Y.)
container_volume 178
creator Jupin, I.
Richards, K.
Jonard, G.
Guilley, H.
Pleij, C.W.A.
description Of the four genome components of beet necrotic yellow vein virus only RNAs 1 and 2 are essential for viral replication in leaves. We have mapped cis-regulatory elements on RNA 3 by introducing deletions into expressible cDNA clones and inoculating leaves with the altered transcripts along with RNAs 1 and 2. Transcripts carrying internal deletions extending to within 69 residues of the 3′ poly(A) tail or to within about 300 residues of the 5′ terminus were efficiently amplified and encapsidated in vivo. The 3′ terminal cis-essential domain can be folded into a secondary structure which is conserved among all four genomic RNAs and which probably contains the minus-strand promoter. RNA 3 transcripts with 75% of the central core of the sequence deleted or replaced by the β-glucuronidase (GUS) gene were also viable. GUS activity was detected in infected tissue in the latter case.
doi_str_mv 10.1016/0042-6822(90)90403-E
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_79957260</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>004268229090403E</els_id><sourcerecordid>79957260</sourcerecordid><originalsourceid>FETCH-LOGICAL-c437t-e4d43561498cba55412f8910bc671b159ecdd93fc55741523cd1ee5d19e8196d3</originalsourceid><addsrcrecordid>eNqFkU1v1DAQhi0EKkvhDyCQfCmCQ8Djr8QXpKraAlILEtArlmNPKqNsEuxkq_77etlVudGTP95nXs28Q8grYO-Bgf7AmOSVbjh_a9g7wyQT1foRWQEzumJCwmOyukeekmc5_2blXdfsiBxx0RilxIr8unTTFIdrmvHPgoPHTFO5xYSBdmOiUxrD4ue4xfI_9dG7OY4DHTvaIs50QJ_GOXp6i30_3tAtxoFuY1oy_f71lIrn5Enn-owvDucxuTpf_zz7XF18-_Tl7PSi8lLUc4UySKE0SNP41iklgXeNAdZ6XUMLyqAPwYjOK1VLUFz4AIgqgMEGjA7imLzZ-5Z-yxx5tpuYfenJDTgu2dbGqJpr9iAIGngtuS6g3INlwJwTdnZKcePSrQVmd_nbXbh2F641zP7N365L2euD_9JuMNwXHQIv-slBd9m7vktu8DH_8zaK66apC_dyz3VutO46FebqhwHgUkARP-5FLJFuIyabfdwtL5S9-dmGMf6_yzvbKqkk</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>16127426</pqid></control><display><type>article</type><title>Mapping sequences required for productive replication of beet necrotic yellow vein virus RNA 3</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Jupin, I. ; Richards, K. ; Jonard, G. ; Guilley, H. ; Pleij, C.W.A.</creator><creatorcontrib>Jupin, I. ; Richards, K. ; Jonard, G. ; Guilley, H. ; Pleij, C.W.A.</creatorcontrib><description>Of the four genome components of beet necrotic yellow vein virus only RNAs 1 and 2 are essential for viral replication in leaves. We have mapped cis-regulatory elements on RNA 3 by introducing deletions into expressible cDNA clones and inoculating leaves with the altered transcripts along with RNAs 1 and 2. Transcripts carrying internal deletions extending to within 69 residues of the 3′ poly(A) tail or to within about 300 residues of the 5′ terminus were efficiently amplified and encapsidated in vivo. The 3′ terminal cis-essential domain can be folded into a secondary structure which is conserved among all four genomic RNAs and which probably contains the minus-strand promoter. RNA 3 transcripts with 75% of the central core of the sequence deleted or replaced by the β-glucuronidase (GUS) gene were also viable. GUS activity was detected in infected tissue in the latter case.</description><identifier>ISSN: 0042-6822</identifier><identifier>EISSN: 1096-0341</identifier><identifier>DOI: 10.1016/0042-6822(90)90403-E</identifier><identifier>PMID: 2389553</identifier><identifier>CODEN: VIRLAX</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>ARN ; Base Sequence ; Biological and medical sciences ; CHENOPODIUM QUINOA ; Chromosome Deletion ; DNA Replication ; FEUILLE ; Fundamental and applied biological sciences. Psychology ; Genes, Viral ; Genetics ; Glucuronidase - biosynthesis ; Glucuronidase - genetics ; HOJAS ; LEAVES ; Microbiology ; MOLECULAR SEQUENCE DATA ; Nucleic Acid Conformation ; NUCLEOTIDE ; Nucleotide Mapping ; NUCLEOTIDES ; NUCLEOTIDOS ; PLANT VIRUSES ; Plant Viruses - genetics ; RNA ; RNA AMPLIFICATION ; RNA, Viral - biosynthesis ; Sequence Homology, Nucleic Acid ; Transcription, Genetic ; Virology ; VIRUS DE LAS PLANTAS ; VIRUS DES VEGETAUX ; Virus Replication</subject><ispartof>Virology (New York, N.Y.), 1990-09, Vol.178 (1), p.273-280</ispartof><rights>1990</rights><rights>1991 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c437t-e4d43561498cba55412f8910bc671b159ecdd93fc55741523cd1ee5d19e8196d3</citedby><cites>FETCH-LOGICAL-c437t-e4d43561498cba55412f8910bc671b159ecdd93fc55741523cd1ee5d19e8196d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0042-6822(90)90403-E$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3536,27903,27904,45974</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=19526887$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2389553$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jupin, I.</creatorcontrib><creatorcontrib>Richards, K.</creatorcontrib><creatorcontrib>Jonard, G.</creatorcontrib><creatorcontrib>Guilley, H.</creatorcontrib><creatorcontrib>Pleij, C.W.A.</creatorcontrib><title>Mapping sequences required for productive replication of beet necrotic yellow vein virus RNA 3</title><title>Virology (New York, N.Y.)</title><addtitle>Virology</addtitle><description>Of the four genome components of beet necrotic yellow vein virus only RNAs 1 and 2 are essential for viral replication in leaves. We have mapped cis-regulatory elements on RNA 3 by introducing deletions into expressible cDNA clones and inoculating leaves with the altered transcripts along with RNAs 1 and 2. Transcripts carrying internal deletions extending to within 69 residues of the 3′ poly(A) tail or to within about 300 residues of the 5′ terminus were efficiently amplified and encapsidated in vivo. The 3′ terminal cis-essential domain can be folded into a secondary structure which is conserved among all four genomic RNAs and which probably contains the minus-strand promoter. RNA 3 transcripts with 75% of the central core of the sequence deleted or replaced by the β-glucuronidase (GUS) gene were also viable. GUS activity was detected in infected tissue in the latter case.</description><subject>ARN</subject><subject>Base Sequence</subject><subject>Biological and medical sciences</subject><subject>CHENOPODIUM QUINOA</subject><subject>Chromosome Deletion</subject><subject>DNA Replication</subject><subject>FEUILLE</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genes, Viral</subject><subject>Genetics</subject><subject>Glucuronidase - biosynthesis</subject><subject>Glucuronidase - genetics</subject><subject>HOJAS</subject><subject>LEAVES</subject><subject>Microbiology</subject><subject>MOLECULAR SEQUENCE DATA</subject><subject>Nucleic Acid Conformation</subject><subject>NUCLEOTIDE</subject><subject>Nucleotide Mapping</subject><subject>NUCLEOTIDES</subject><subject>NUCLEOTIDOS</subject><subject>PLANT VIRUSES</subject><subject>Plant Viruses - genetics</subject><subject>RNA</subject><subject>RNA AMPLIFICATION</subject><subject>RNA, Viral - biosynthesis</subject><subject>Sequence Homology, Nucleic Acid</subject><subject>Transcription, Genetic</subject><subject>Virology</subject><subject>VIRUS DE LAS PLANTAS</subject><subject>VIRUS DES VEGETAUX</subject><subject>Virus Replication</subject><issn>0042-6822</issn><issn>1096-0341</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkU1v1DAQhi0EKkvhDyCQfCmCQ8Djr8QXpKraAlILEtArlmNPKqNsEuxkq_77etlVudGTP95nXs28Q8grYO-Bgf7AmOSVbjh_a9g7wyQT1foRWQEzumJCwmOyukeekmc5_2blXdfsiBxx0RilxIr8unTTFIdrmvHPgoPHTFO5xYSBdmOiUxrD4ue4xfI_9dG7OY4DHTvaIs50QJ_GOXp6i30_3tAtxoFuY1oy_f71lIrn5Enn-owvDucxuTpf_zz7XF18-_Tl7PSi8lLUc4UySKE0SNP41iklgXeNAdZ6XUMLyqAPwYjOK1VLUFz4AIgqgMEGjA7imLzZ-5Z-yxx5tpuYfenJDTgu2dbGqJpr9iAIGngtuS6g3INlwJwTdnZKcePSrQVmd_nbXbh2F641zP7N365L2euD_9JuMNwXHQIv-slBd9m7vktu8DH_8zaK66apC_dyz3VutO46FebqhwHgUkARP-5FLJFuIyabfdwtL5S9-dmGMf6_yzvbKqkk</recordid><startdate>19900901</startdate><enddate>19900901</enddate><creator>Jupin, I.</creator><creator>Richards, K.</creator><creator>Jonard, G.</creator><creator>Guilley, H.</creator><creator>Pleij, C.W.A.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>FBQ</scope><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>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19900901</creationdate><title>Mapping sequences required for productive replication of beet necrotic yellow vein virus RNA 3</title><author>Jupin, I. ; Richards, K. ; Jonard, G. ; Guilley, H. ; Pleij, C.W.A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c437t-e4d43561498cba55412f8910bc671b159ecdd93fc55741523cd1ee5d19e8196d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>ARN</topic><topic>Base Sequence</topic><topic>Biological and medical sciences</topic><topic>CHENOPODIUM QUINOA</topic><topic>Chromosome Deletion</topic><topic>DNA Replication</topic><topic>FEUILLE</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genes, Viral</topic><topic>Genetics</topic><topic>Glucuronidase - biosynthesis</topic><topic>Glucuronidase - genetics</topic><topic>HOJAS</topic><topic>LEAVES</topic><topic>Microbiology</topic><topic>MOLECULAR SEQUENCE DATA</topic><topic>Nucleic Acid Conformation</topic><topic>NUCLEOTIDE</topic><topic>Nucleotide Mapping</topic><topic>NUCLEOTIDES</topic><topic>NUCLEOTIDOS</topic><topic>PLANT VIRUSES</topic><topic>Plant Viruses - genetics</topic><topic>RNA</topic><topic>RNA AMPLIFICATION</topic><topic>RNA, Viral - biosynthesis</topic><topic>Sequence Homology, Nucleic Acid</topic><topic>Transcription, Genetic</topic><topic>Virology</topic><topic>VIRUS DE LAS PLANTAS</topic><topic>VIRUS DES VEGETAUX</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jupin, I.</creatorcontrib><creatorcontrib>Richards, K.</creatorcontrib><creatorcontrib>Jonard, G.</creatorcontrib><creatorcontrib>Guilley, H.</creatorcontrib><creatorcontrib>Pleij, C.W.A.</creatorcontrib><collection>AGRIS</collection><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>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Virology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jupin, I.</au><au>Richards, K.</au><au>Jonard, G.</au><au>Guilley, H.</au><au>Pleij, C.W.A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Mapping sequences required for productive replication of beet necrotic yellow vein virus RNA 3</atitle><jtitle>Virology (New York, N.Y.)</jtitle><addtitle>Virology</addtitle><date>1990-09-01</date><risdate>1990</risdate><volume>178</volume><issue>1</issue><spage>273</spage><epage>280</epage><pages>273-280</pages><issn>0042-6822</issn><eissn>1096-0341</eissn><coden>VIRLAX</coden><abstract>Of the four genome components of beet necrotic yellow vein virus only RNAs 1 and 2 are essential for viral replication in leaves. We have mapped cis-regulatory elements on RNA 3 by introducing deletions into expressible cDNA clones and inoculating leaves with the altered transcripts along with RNAs 1 and 2. Transcripts carrying internal deletions extending to within 69 residues of the 3′ poly(A) tail or to within about 300 residues of the 5′ terminus were efficiently amplified and encapsidated in vivo. The 3′ terminal cis-essential domain can be folded into a secondary structure which is conserved among all four genomic RNAs and which probably contains the minus-strand promoter. RNA 3 transcripts with 75% of the central core of the sequence deleted or replaced by the β-glucuronidase (GUS) gene were also viable. GUS activity was detected in infected tissue in the latter case.</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>2389553</pmid><doi>10.1016/0042-6822(90)90403-E</doi><tpages>8</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0042-6822
ispartof Virology (New York, N.Y.), 1990-09, Vol.178 (1), p.273-280
issn 0042-6822
1096-0341
language eng
recordid cdi_proquest_miscellaneous_79957260
source MEDLINE; Elsevier ScienceDirect Journals Complete; EZB-FREE-00999 freely available EZB journals
subjects ARN
Base Sequence
Biological and medical sciences
CHENOPODIUM QUINOA
Chromosome Deletion
DNA Replication
FEUILLE
Fundamental and applied biological sciences. Psychology
Genes, Viral
Genetics
Glucuronidase - biosynthesis
Glucuronidase - genetics
HOJAS
LEAVES
Microbiology
MOLECULAR SEQUENCE DATA
Nucleic Acid Conformation
NUCLEOTIDE
Nucleotide Mapping
NUCLEOTIDES
NUCLEOTIDOS
PLANT VIRUSES
Plant Viruses - genetics
RNA
RNA AMPLIFICATION
RNA, Viral - biosynthesis
Sequence Homology, Nucleic Acid
Transcription, Genetic
Virology
VIRUS DE LAS PLANTAS
VIRUS DES VEGETAUX
Virus Replication
title Mapping sequences required for productive replication of beet necrotic yellow vein virus RNA 3
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T01%3A24%3A43IST&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=Mapping%20sequences%20required%20for%20productive%20replication%20of%20beet%20necrotic%20yellow%20vein%20virus%20RNA%203&rft.jtitle=Virology%20(New%20York,%20N.Y.)&rft.au=Jupin,%20I.&rft.date=1990-09-01&rft.volume=178&rft.issue=1&rft.spage=273&rft.epage=280&rft.pages=273-280&rft.issn=0042-6822&rft.eissn=1096-0341&rft.coden=VIRLAX&rft_id=info:doi/10.1016/0042-6822(90)90403-E&rft_dat=%3Cproquest_cross%3E79957260%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=16127426&rft_id=info:pmid/2389553&rft_els_id=004268229090403E&rfr_iscdi=true