Turnip mosaic potyvirus resistance in Nicotiana benthamiana derived by post-transcriptional gene silencing

The coat protein (CP) gene of turnip mosaic potyvirus isolate ESC8 (TuMV-ESC8) was cloned and sequenced. Comparisons of the 867-nucleotide (nt) CP region with those of 11 TuMV isolates showed 86.7-89.3% nucleotide identity and 92.4-95.5% amino acid identity. The CP gene was cloned into a plant expre...

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Veröffentlicht in:Transgenic research 1999-06, Vol.8 (3), p.203-213
Hauptverfasser: JAN, F.-J, PANG, S.-Z, FAGOAGA, C, GONSALVES, D
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PANG, S.-Z
FAGOAGA, C
GONSALVES, D
description The coat protein (CP) gene of turnip mosaic potyvirus isolate ESC8 (TuMV-ESC8) was cloned and sequenced. Comparisons of the 867-nucleotide (nt) CP region with those of 11 TuMV isolates showed 86.7-89.3% nucleotide identity and 92.4-95.5% amino acid identity. The CP gene was cloned into a plant expression vector and transformed into Nicotiana benthamiana plants via Agrobacterium tumefaciens-mediated leaf disk transformation. Progeny from R0 lines was screened for resistance to TuMV-ESC8. Five of 29 tested lines showed TuMV protection in more than 50% of their progeny. Interestingly, some of the resistant plants transformed with the CP gene of TuMV displayed mild mosaicism in the new growing leaves at the later stages of evaluation; but these mosaic symptoms disappeared when the leaves were fully expanded. Collective data from steady-state RNA analysis and nuclear run-on assay of a line showed that the resistance was RNA-mediated through the post-transcriptional gene silencing mechanism.
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Comparisons of the 867-nucleotide (nt) CP region with those of 11 TuMV isolates showed 86.7-89.3% nucleotide identity and 92.4-95.5% amino acid identity. The CP gene was cloned into a plant expression vector and transformed into Nicotiana benthamiana plants via Agrobacterium tumefaciens-mediated leaf disk transformation. Progeny from R0 lines was screened for resistance to TuMV-ESC8. Five of 29 tested lines showed TuMV protection in more than 50% of their progeny. Interestingly, some of the resistant plants transformed with the CP gene of TuMV displayed mild mosaicism in the new growing leaves at the later stages of evaluation; but these mosaic symptoms disappeared when the leaves were fully expanded. Collective data from steady-state RNA analysis and nuclear run-on assay of a line showed that the resistance was RNA-mediated through the post-transcriptional gene silencing mechanism.</description><identifier>ISSN: 0962-8819</identifier><identifier>EISSN: 1573-9368</identifier><identifier>DOI: 10.1023/A:1008915007271</identifier><identifier>PMID: 10478490</identifier><language>eng</language><publisher>Dordrecht: Springer</publisher><subject>Amino Acid Sequence ; Bacteria ; Base Sequence ; Biological and medical sciences ; Biotechnology ; Capsid - genetics ; Cloning, Molecular ; Fundamental and applied biological sciences. Psychology ; Generalities. Techniques. Transmission, epidemiology, ecology. Antiviral substances, control ; Genes ; Genetic engineering ; Genetic technics ; Methods. Procedures. Technologies ; Molecular Sequence Data ; Nicotiana - genetics ; Nicotiana - growth &amp; development ; Nicotiana - virology ; Nicotiana benthamiana ; Phytopathology. Animal pests. Plant and forest protection ; Plant Diseases - virology ; Plant viruses and viroids ; Plants, Genetically Modified - virology ; Plants, Toxic ; Potyvirus - genetics ; Proteins ; Sequence Analysis, DNA ; Transcription, Genetic ; Transformation, Genetic ; Transgenes ; Transgenic animals and transgenic plants ; Transgenic plants ; Turnip mosaic virus</subject><ispartof>Transgenic research, 1999-06, Vol.8 (3), p.203-213</ispartof><rights>2000 INIST-CNRS</rights><rights>Kluwer Academic Publishers 1999</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-8de7140a1a5409e5e0f89c9ac9dccd2c7a05f52568443ef028c30eea4166fe013</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=1195864$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10478490$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>JAN, F.-J</creatorcontrib><creatorcontrib>PANG, S.-Z</creatorcontrib><creatorcontrib>FAGOAGA, C</creatorcontrib><creatorcontrib>GONSALVES, D</creatorcontrib><title>Turnip mosaic potyvirus resistance in Nicotiana benthamiana derived by post-transcriptional gene silencing</title><title>Transgenic research</title><addtitle>Transgenic Res</addtitle><description>The coat protein (CP) gene of turnip mosaic potyvirus isolate ESC8 (TuMV-ESC8) was cloned and sequenced. Comparisons of the 867-nucleotide (nt) CP region with those of 11 TuMV isolates showed 86.7-89.3% nucleotide identity and 92.4-95.5% amino acid identity. The CP gene was cloned into a plant expression vector and transformed into Nicotiana benthamiana plants via Agrobacterium tumefaciens-mediated leaf disk transformation. Progeny from R0 lines was screened for resistance to TuMV-ESC8. Five of 29 tested lines showed TuMV protection in more than 50% of their progeny. Interestingly, some of the resistant plants transformed with the CP gene of TuMV displayed mild mosaicism in the new growing leaves at the later stages of evaluation; but these mosaic symptoms disappeared when the leaves were fully expanded. 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Plant and forest protection</topic><topic>Plant Diseases - virology</topic><topic>Plant viruses and viroids</topic><topic>Plants, Genetically Modified - virology</topic><topic>Plants, Toxic</topic><topic>Potyvirus - genetics</topic><topic>Proteins</topic><topic>Sequence Analysis, DNA</topic><topic>Transcription, Genetic</topic><topic>Transformation, Genetic</topic><topic>Transgenes</topic><topic>Transgenic animals and transgenic plants</topic><topic>Transgenic plants</topic><topic>Turnip mosaic virus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>JAN, F.-J</creatorcontrib><creatorcontrib>PANG, S.-Z</creatorcontrib><creatorcontrib>FAGOAGA, C</creatorcontrib><creatorcontrib>GONSALVES, D</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>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>Genetics Abstracts</collection><collection>Biotechnology Research Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Transgenic research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>JAN, F.-J</au><au>PANG, S.-Z</au><au>FAGOAGA, C</au><au>GONSALVES, D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Turnip mosaic potyvirus resistance in Nicotiana benthamiana derived by post-transcriptional gene silencing</atitle><jtitle>Transgenic research</jtitle><addtitle>Transgenic Res</addtitle><date>1999-06-01</date><risdate>1999</risdate><volume>8</volume><issue>3</issue><spage>203</spage><epage>213</epage><pages>203-213</pages><issn>0962-8819</issn><eissn>1573-9368</eissn><abstract>The coat protein (CP) gene of turnip mosaic potyvirus isolate ESC8 (TuMV-ESC8) was cloned and sequenced. Comparisons of the 867-nucleotide (nt) CP region with those of 11 TuMV isolates showed 86.7-89.3% nucleotide identity and 92.4-95.5% amino acid identity. The CP gene was cloned into a plant expression vector and transformed into Nicotiana benthamiana plants via Agrobacterium tumefaciens-mediated leaf disk transformation. Progeny from R0 lines was screened for resistance to TuMV-ESC8. Five of 29 tested lines showed TuMV protection in more than 50% of their progeny. Interestingly, some of the resistant plants transformed with the CP gene of TuMV displayed mild mosaicism in the new growing leaves at the later stages of evaluation; but these mosaic symptoms disappeared when the leaves were fully expanded. Collective data from steady-state RNA analysis and nuclear run-on assay of a line showed that the resistance was RNA-mediated through the post-transcriptional gene silencing mechanism.</abstract><cop>Dordrecht</cop><pub>Springer</pub><pmid>10478490</pmid><doi>10.1023/A:1008915007271</doi><tpages>11</tpages></addata></record>
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subjects Amino Acid Sequence
Bacteria
Base Sequence
Biological and medical sciences
Biotechnology
Capsid - genetics
Cloning, Molecular
Fundamental and applied biological sciences. Psychology
Generalities. Techniques. Transmission, epidemiology, ecology. Antiviral substances, control
Genes
Genetic engineering
Genetic technics
Methods. Procedures. Technologies
Molecular Sequence Data
Nicotiana - genetics
Nicotiana - growth & development
Nicotiana - virology
Nicotiana benthamiana
Phytopathology. Animal pests. Plant and forest protection
Plant Diseases - virology
Plant viruses and viroids
Plants, Genetically Modified - virology
Plants, Toxic
Potyvirus - genetics
Proteins
Sequence Analysis, DNA
Transcription, Genetic
Transformation, Genetic
Transgenes
Transgenic animals and transgenic plants
Transgenic plants
Turnip mosaic virus
title Turnip mosaic potyvirus resistance in Nicotiana benthamiana derived by post-transcriptional gene silencing
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