Artificial Defective Interfering RNAs Derived from Brome Mosaic Virus
Department of Biology, Texas A&M University, College Station, Texas 77843-3258, U.S.A. Naturally occurring defective interfering RNAs (DI-RNAs) greatly reduce the accumulation of their helper virus in vivo , but are rarely associated with plant positive-strand RNA viruses. Deletion mutants pRNA-...
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Veröffentlicht in: | Journal of general virology 1991-08, Vol.72 (8), p.1787-1792 |
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container_title | Journal of general virology |
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creator | Marsh, Loren E Pogue, Gregory P Connell, James P Hall, Timothy C |
description | Department of Biology, Texas A&M University, College Station, Texas 77843-3258, U.S.A.
Naturally occurring defective interfering RNAs (DI-RNAs) greatly reduce the accumulation of their helper virus in vivo , but are rarely associated with plant positive-strand RNA viruses. Deletion mutants pRNA-2 M/S and pRNA-2 E/S, derived from brome mosaic virus (BMV) genomic RNA-2, replicated in a manner dependent on BMV RNA-1 and -2, and effectively interfered with their accumulation in barley protoplasts. Based on their mode of replication, these mutant RNAs have been termed parasitic RNAs (pRNAs). When present with RNA-1 and -2 at low inoculum amounts, pRNA-2 M/S and pRNA-2 E/S reduced the level of replication of RNA-2, the parental RNA, by 37% and 64%, respectively. Greater amounts of pRNA in the inoculum completely eliminated the replication of both RNA-1 and -2. Mutations that prevented translation of truncated proteins from the pRNAs did not affect interference, but those that reduced pRNA replication decreased their ability to interfere with genomic RNA replication. At a molar pRNA: genomic RNA inoculum ratio of 1.5:1, pRNA-2 E/S reduced the accumulation of all helper virus RNAs by > 60%. This occurred in the presence of wild-type RNA-3 or SGP RNA-3, a deletion mutant of RNA-3 that lacks the subgenomic promoter necessary for coat protein expression, demonstrating that the interference mediated by the pRNAs was not effected by encapsidation. These data indicate that the expression of pRNAs that function as artificial DI-RNAs in transgenic plants may be an approach for inducing resistance to virus infection which is applicable to a wide range of plant viruses.
Received 18 February 1991;
accepted 23 April 1991. |
doi_str_mv | 10.1099/0022-1317-72-8-1787 |
format | Article |
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Naturally occurring defective interfering RNAs (DI-RNAs) greatly reduce the accumulation of their helper virus in vivo , but are rarely associated with plant positive-strand RNA viruses. Deletion mutants pRNA-2 M/S and pRNA-2 E/S, derived from brome mosaic virus (BMV) genomic RNA-2, replicated in a manner dependent on BMV RNA-1 and -2, and effectively interfered with their accumulation in barley protoplasts. Based on their mode of replication, these mutant RNAs have been termed parasitic RNAs (pRNAs). When present with RNA-1 and -2 at low inoculum amounts, pRNA-2 M/S and pRNA-2 E/S reduced the level of replication of RNA-2, the parental RNA, by 37% and 64%, respectively. Greater amounts of pRNA in the inoculum completely eliminated the replication of both RNA-1 and -2. Mutations that prevented translation of truncated proteins from the pRNAs did not affect interference, but those that reduced pRNA replication decreased their ability to interfere with genomic RNA replication. At a molar pRNA: genomic RNA inoculum ratio of 1.5:1, pRNA-2 E/S reduced the accumulation of all helper virus RNAs by > 60%. This occurred in the presence of wild-type RNA-3 or SGP RNA-3, a deletion mutant of RNA-3 that lacks the subgenomic promoter necessary for coat protein expression, demonstrating that the interference mediated by the pRNAs was not effected by encapsidation. These data indicate that the expression of pRNAs that function as artificial DI-RNAs in transgenic plants may be an approach for inducing resistance to virus infection which is applicable to a wide range of plant viruses.
Received 18 February 1991;
accepted 23 April 1991.</description><identifier>ISSN: 0022-1317</identifier><identifier>EISSN: 1465-2099</identifier><identifier>DOI: 10.1099/0022-1317-72-8-1787</identifier><identifier>PMID: 1875191</identifier><identifier>CODEN: JGVIAY</identifier><language>eng</language><publisher>Reading: Soc General Microbiol</publisher><subject>Biological and medical sciences ; Blotting, Northern ; brome mosaic virus ; Chromosome Deletion ; Codon ; Fundamental and applied biological sciences. Psychology ; Genetics ; Helper Viruses - physiology ; Hordeum ; Microbiology ; Mosaic Viruses - genetics ; Mosaic Viruses - physiology ; Mutagenesis ; Plasmids ; Protoplasts ; RNA, Viral - biosynthesis ; RNA, Viral - genetics ; RNA, Viral - isolation & purification ; Virology ; Virus Replication</subject><ispartof>Journal of general virology, 1991-08, Vol.72 (8), p.1787-1792</ispartof><rights>1992 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-eadf0161b59acbc41fdf027a55710eaca60d9e0c56c5810a457ced0e3c57757b3</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&idt=5006151$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/1875191$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marsh, Loren E</creatorcontrib><creatorcontrib>Pogue, Gregory P</creatorcontrib><creatorcontrib>Connell, James P</creatorcontrib><creatorcontrib>Hall, Timothy C</creatorcontrib><title>Artificial Defective Interfering RNAs Derived from Brome Mosaic Virus</title><title>Journal of general virology</title><addtitle>J Gen Virol</addtitle><description>Department of Biology, Texas A&M University, College Station, Texas 77843-3258, U.S.A.
Naturally occurring defective interfering RNAs (DI-RNAs) greatly reduce the accumulation of their helper virus in vivo , but are rarely associated with plant positive-strand RNA viruses. Deletion mutants pRNA-2 M/S and pRNA-2 E/S, derived from brome mosaic virus (BMV) genomic RNA-2, replicated in a manner dependent on BMV RNA-1 and -2, and effectively interfered with their accumulation in barley protoplasts. Based on their mode of replication, these mutant RNAs have been termed parasitic RNAs (pRNAs). When present with RNA-1 and -2 at low inoculum amounts, pRNA-2 M/S and pRNA-2 E/S reduced the level of replication of RNA-2, the parental RNA, by 37% and 64%, respectively. Greater amounts of pRNA in the inoculum completely eliminated the replication of both RNA-1 and -2. Mutations that prevented translation of truncated proteins from the pRNAs did not affect interference, but those that reduced pRNA replication decreased their ability to interfere with genomic RNA replication. At a molar pRNA: genomic RNA inoculum ratio of 1.5:1, pRNA-2 E/S reduced the accumulation of all helper virus RNAs by > 60%. This occurred in the presence of wild-type RNA-3 or SGP RNA-3, a deletion mutant of RNA-3 that lacks the subgenomic promoter necessary for coat protein expression, demonstrating that the interference mediated by the pRNAs was not effected by encapsidation. These data indicate that the expression of pRNAs that function as artificial DI-RNAs in transgenic plants may be an approach for inducing resistance to virus infection which is applicable to a wide range of plant viruses.
Received 18 February 1991;
accepted 23 April 1991.</description><subject>Biological and medical sciences</subject><subject>Blotting, Northern</subject><subject>brome mosaic virus</subject><subject>Chromosome Deletion</subject><subject>Codon</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Genetics</subject><subject>Helper Viruses - physiology</subject><subject>Hordeum</subject><subject>Microbiology</subject><subject>Mosaic Viruses - genetics</subject><subject>Mosaic Viruses - physiology</subject><subject>Mutagenesis</subject><subject>Plasmids</subject><subject>Protoplasts</subject><subject>RNA, Viral - biosynthesis</subject><subject>RNA, Viral - genetics</subject><subject>RNA, Viral - isolation & purification</subject><subject>Virology</subject><subject>Virus Replication</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>eNpFkMtKxDAUhoMoOo4-gQhdiLipntM2Tbsc7wNeQNRtSNOTMdKLJh3FtzdlBt0kJP93LnyMHSCcIpTlGUCSxJiiiEUSFzGKQmywCWY5j5OQb7LJH7HDdr1_B8As42KbbWMhOJY4YVczN1hjtVVNdEmG9GC_KJp3AzlDznaL6Olh5kPkwn8dGde30Xk4KLrvvbI6erVu6ffYllGNp_31PWUv11fPF7fx3ePN_GJ2F-ssLYaYVG0Ac6x4qXSlMzThnQjFuUAgpVUOdUmgea55gaDCrppqoFRzIbio0ik7XvX9cP3nkvwgW-s1NY3qqF96iTmAAMgCmK5A7XrvHRn54Wyr3I9EkKM8OaqRoxopElnIUV6oOly3X1Yt1f81K1shP1rnymvVGKc6bf0fxgFy5CN2ssLe7OLt2zqSC-paG1apbC-_rPuf-Asht4Rd</recordid><startdate>19910801</startdate><enddate>19910801</enddate><creator>Marsh, Loren E</creator><creator>Pogue, Gregory P</creator><creator>Connell, James P</creator><creator>Hall, Timothy 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>7TM</scope><scope>7U9</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>P64</scope><scope>RC3</scope></search><sort><creationdate>19910801</creationdate><title>Artificial Defective Interfering RNAs Derived from Brome Mosaic Virus</title><author>Marsh, Loren E ; Pogue, Gregory P ; Connell, James P ; Hall, Timothy C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-eadf0161b59acbc41fdf027a55710eaca60d9e0c56c5810a457ced0e3c57757b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1991</creationdate><topic>Biological and medical sciences</topic><topic>Blotting, Northern</topic><topic>brome mosaic virus</topic><topic>Chromosome Deletion</topic><topic>Codon</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Genetics</topic><topic>Helper Viruses - physiology</topic><topic>Hordeum</topic><topic>Microbiology</topic><topic>Mosaic Viruses - genetics</topic><topic>Mosaic Viruses - physiology</topic><topic>Mutagenesis</topic><topic>Plasmids</topic><topic>Protoplasts</topic><topic>RNA, Viral - biosynthesis</topic><topic>RNA, Viral - genetics</topic><topic>RNA, Viral - isolation & purification</topic><topic>Virology</topic><topic>Virus Replication</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marsh, Loren E</creatorcontrib><creatorcontrib>Pogue, Gregory P</creatorcontrib><creatorcontrib>Connell, James P</creatorcontrib><creatorcontrib>Hall, Timothy 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>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><jtitle>Journal of general virology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marsh, Loren E</au><au>Pogue, Gregory P</au><au>Connell, James P</au><au>Hall, Timothy C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Artificial Defective Interfering RNAs Derived from Brome Mosaic Virus</atitle><jtitle>Journal of general virology</jtitle><addtitle>J Gen Virol</addtitle><date>1991-08-01</date><risdate>1991</risdate><volume>72</volume><issue>8</issue><spage>1787</spage><epage>1792</epage><pages>1787-1792</pages><issn>0022-1317</issn><eissn>1465-2099</eissn><coden>JGVIAY</coden><abstract>Department of Biology, Texas A&M University, College Station, Texas 77843-3258, U.S.A.
Naturally occurring defective interfering RNAs (DI-RNAs) greatly reduce the accumulation of their helper virus in vivo , but are rarely associated with plant positive-strand RNA viruses. Deletion mutants pRNA-2 M/S and pRNA-2 E/S, derived from brome mosaic virus (BMV) genomic RNA-2, replicated in a manner dependent on BMV RNA-1 and -2, and effectively interfered with their accumulation in barley protoplasts. Based on their mode of replication, these mutant RNAs have been termed parasitic RNAs (pRNAs). When present with RNA-1 and -2 at low inoculum amounts, pRNA-2 M/S and pRNA-2 E/S reduced the level of replication of RNA-2, the parental RNA, by 37% and 64%, respectively. Greater amounts of pRNA in the inoculum completely eliminated the replication of both RNA-1 and -2. Mutations that prevented translation of truncated proteins from the pRNAs did not affect interference, but those that reduced pRNA replication decreased their ability to interfere with genomic RNA replication. At a molar pRNA: genomic RNA inoculum ratio of 1.5:1, pRNA-2 E/S reduced the accumulation of all helper virus RNAs by > 60%. This occurred in the presence of wild-type RNA-3 or SGP RNA-3, a deletion mutant of RNA-3 that lacks the subgenomic promoter necessary for coat protein expression, demonstrating that the interference mediated by the pRNAs was not effected by encapsidation. These data indicate that the expression of pRNAs that function as artificial DI-RNAs in transgenic plants may be an approach for inducing resistance to virus infection which is applicable to a wide range of plant viruses.
Received 18 February 1991;
accepted 23 April 1991.</abstract><cop>Reading</cop><pub>Soc General Microbiol</pub><pmid>1875191</pmid><doi>10.1099/0022-1317-72-8-1787</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Biological and medical sciences Blotting, Northern brome mosaic virus Chromosome Deletion Codon Fundamental and applied biological sciences. Psychology Genetics Helper Viruses - physiology Hordeum Microbiology Mosaic Viruses - genetics Mosaic Viruses - physiology Mutagenesis Plasmids Protoplasts RNA, Viral - biosynthesis RNA, Viral - genetics RNA, Viral - isolation & purification Virology Virus Replication |
title | Artificial Defective Interfering RNAs Derived from Brome Mosaic Virus |
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