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Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor
Abstract Host RNA-binding proteins are likely to play multiple, integral roles during replication of plus-strand RNA viruses. To identify host proteins that bind to viral RNAs, we took a global approach based on the yeast proteome microarray, which contains 4080 purified yeast proteins. The biotin-l...
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Published in: | Virology (New York, N.Y.) N.Y.), 2009-03, Vol.385 (1), p.245-260 |
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description | Abstract Host RNA-binding proteins are likely to play multiple, integral roles during replication of plus-strand RNA viruses. To identify host proteins that bind to viral RNAs, we took a global approach based on the yeast proteome microarray, which contains 4080 purified yeast proteins. The biotin-labeled RNA probes included two distantly related RNA viruses, namely Tomato bushy stunt virus (TBSV) and Brome mosaic virus (BMV). Altogether, we have identified 57 yeast proteins that bound to TBSV RNA and/or BMV RNA. Among the identified host proteins, eleven bound to TBSV RNA and seven bound to BMV RNA with high selectivity, whereas the remaining 39 host proteins bound to both viral RNAs. The interaction between the TBSV replicon RNA and five of the identified host proteins was confirmed via gel-mobility shift and co-purification experiments from yeast. Over-expression of the host proteins in yeast, a model host for TBSV, revealed 4 host proteins that enhanced TBSV replication as well as 14 proteins that inhibited replication. Detailed analysis of one of the identified yeast proteins binding to TBSV RNA, namely translation elongation factor eEF1A, revealed that it is present in the highly purified tombusvirus replicase complex. We also demonstrate binding of eEF1A to the p33 replication protein and a known cis-acting element at the 3′ end of TBSV RNA. Using a functional mutant of eEF1A, we provide evidence on the involvement of eEF1A in TBSV replication. |
doi_str_mv | 10.1016/j.virol.2008.11.041 |
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To identify host proteins that bind to viral RNAs, we took a global approach based on the yeast proteome microarray, which contains 4080 purified yeast proteins. The biotin-labeled RNA probes included two distantly related RNA viruses, namely Tomato bushy stunt virus (TBSV) and Brome mosaic virus (BMV). Altogether, we have identified 57 yeast proteins that bound to TBSV RNA and/or BMV RNA. Among the identified host proteins, eleven bound to TBSV RNA and seven bound to BMV RNA with high selectivity, whereas the remaining 39 host proteins bound to both viral RNAs. The interaction between the TBSV replicon RNA and five of the identified host proteins was confirmed via gel-mobility shift and co-purification experiments from yeast. Over-expression of the host proteins in yeast, a model host for TBSV, revealed 4 host proteins that enhanced TBSV replication as well as 14 proteins that inhibited replication. Detailed analysis of one of the identified yeast proteins binding to TBSV RNA, namely translation elongation factor eEF1A, revealed that it is present in the highly purified tombusvirus replicase complex. We also demonstrate binding of eEF1A to the p33 replication protein and a known cis-acting element at the 3′ end of TBSV RNA. Using a functional mutant of eEF1A, we provide evidence on the involvement of eEF1A in TBSV replication.</description><identifier>ISSN: 0042-6822</identifier><identifier>EISSN: 1096-0341</identifier><identifier>DOI: 10.1016/j.virol.2008.11.041</identifier><identifier>PMID: 19131084</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>3' Untranslated Regions ; Brome mosaic virus ; Bromovirus - genetics ; Bromovirus - physiology ; eEF1A ; Gene Expression ; Host factor ; Infectious Disease ; Mutation ; Peptide Elongation Factor 1 - genetics ; Peptide Elongation Factor 1 - metabolism ; Protein array ; Proteome array ; Replicase ; Replication ; RNA Replicase - genetics ; RNA Replicase - metabolism ; RNA, Viral - genetics ; RNA, Viral - metabolism ; Silencer Elements, Transcriptional ; TEF1 ; Tomato bushy stunt virus ; Tombusvirus ; Tombusvirus - genetics ; Tombusvirus - physiology ; Ubiquitin-Protein Ligase Complexes - metabolism ; Ubiquitination ; Viral Proteins - metabolism ; Virus Replication - physiology ; Yeast as a model host ; Yeasts - metabolism ; Yeasts - virology</subject><ispartof>Virology (New York, N.Y.), 2009-03, Vol.385 (1), p.245-260</ispartof><rights>2008</rights><rights>2009 Published by Elsevier Inc. 2009</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c609t-c7d861b92d339e95b95851735f06d8015a51f106eaa7615a4edfb18a23b751333</citedby><cites>FETCH-LOGICAL-c609t-c7d861b92d339e95b95851735f06d8015a51f106eaa7615a4edfb18a23b751333</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19131084$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Zhenghe</creatorcontrib><creatorcontrib>Pogany, Judit</creatorcontrib><creatorcontrib>Panavas, Tadas</creatorcontrib><creatorcontrib>Xu, Kai</creatorcontrib><creatorcontrib>Esposito, Anthony M</creatorcontrib><creatorcontrib>Kinzy, Terri Goss</creatorcontrib><creatorcontrib>Nagy, Peter D</creatorcontrib><title>Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor</title><title>Virology (New York, N.Y.)</title><addtitle>Virology</addtitle><description>Abstract Host RNA-binding proteins are likely to play multiple, integral roles during replication of plus-strand RNA viruses. To identify host proteins that bind to viral RNAs, we took a global approach based on the yeast proteome microarray, which contains 4080 purified yeast proteins. The biotin-labeled RNA probes included two distantly related RNA viruses, namely Tomato bushy stunt virus (TBSV) and Brome mosaic virus (BMV). Altogether, we have identified 57 yeast proteins that bound to TBSV RNA and/or BMV RNA. Among the identified host proteins, eleven bound to TBSV RNA and seven bound to BMV RNA with high selectivity, whereas the remaining 39 host proteins bound to both viral RNAs. The interaction between the TBSV replicon RNA and five of the identified host proteins was confirmed via gel-mobility shift and co-purification experiments from yeast. Over-expression of the host proteins in yeast, a model host for TBSV, revealed 4 host proteins that enhanced TBSV replication as well as 14 proteins that inhibited replication. Detailed analysis of one of the identified yeast proteins binding to TBSV RNA, namely translation elongation factor eEF1A, revealed that it is present in the highly purified tombusvirus replicase complex. We also demonstrate binding of eEF1A to the p33 replication protein and a known cis-acting element at the 3′ end of TBSV RNA. Using a functional mutant of eEF1A, we provide evidence on the involvement of eEF1A in TBSV replication.</description><subject>3' Untranslated Regions</subject><subject>Brome mosaic virus</subject><subject>Bromovirus - genetics</subject><subject>Bromovirus - physiology</subject><subject>eEF1A</subject><subject>Gene Expression</subject><subject>Host factor</subject><subject>Infectious Disease</subject><subject>Mutation</subject><subject>Peptide Elongation Factor 1 - genetics</subject><subject>Peptide Elongation Factor 1 - metabolism</subject><subject>Protein array</subject><subject>Proteome array</subject><subject>Replicase</subject><subject>Replication</subject><subject>RNA Replicase - genetics</subject><subject>RNA Replicase - metabolism</subject><subject>RNA, Viral - genetics</subject><subject>RNA, Viral - metabolism</subject><subject>Silencer Elements, Transcriptional</subject><subject>TEF1</subject><subject>Tomato bushy stunt virus</subject><subject>Tombusvirus</subject><subject>Tombusvirus - genetics</subject><subject>Tombusvirus - physiology</subject><subject>Ubiquitin-Protein Ligase Complexes - metabolism</subject><subject>Ubiquitination</subject><subject>Viral Proteins - metabolism</subject><subject>Virus Replication - physiology</subject><subject>Yeast as a model host</subject><subject>Yeasts - metabolism</subject><subject>Yeasts - virology</subject><issn>0042-6822</issn><issn>1096-0341</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqFkstu1DAUhiMEokPhCZCQV-wynBPHcbKgUlVxkyqxoKwtxzlpPXjswU5GzFPwyngu5bbpyj7y_5-Lv1MULxGWCNi8WS23Nga3rADaJeISanxULBC6pgRe4-NiAVBXZdNW1VnxLKUV5FhKeFqcYYccoa0Xxc-bqH1yerLBM3LB3x6vozZTiAwvmU1MMxPWm-DJTyyMbLojNoV1P6fcwJxYpI2zRic6yBz9YNoPTI8jmSkd1GnSvXV22t3bN5zf2w7lTCiPFZ8XT0btEr04nefF1_fvbq4-ltefP3y6urwuTQPdVBo5tA32XTVw3lEn-k60AiUXIzRDCyi0wBGhIa1lk6OahrHHVle8lwI55-fFxTHvZu7XNJg8WtRObaJd67hTQVv174u3d-o2bFUlW1F3TU7w-pQghu8zpUmtbTLknPYU5qSaphNS1uJBYQVcYi3aLORHoYkhpUjj724Q1J64WqkDcbUnrhBVJp5dr_4e5I_nhDgL3h4FlL9zaymqZCx5Q4ONGZAagn2gwMV_fuOsz-DcN9pRWoU5-kxKoUqVAvVlv3T7nYMWQHYo-C-C_NWQ</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Li, Zhenghe</creator><creator>Pogany, Judit</creator><creator>Panavas, Tadas</creator><creator>Xu, Kai</creator><creator>Esposito, Anthony M</creator><creator>Kinzy, Terri Goss</creator><creator>Nagy, Peter D</creator><general>Elsevier Inc</general><scope>6I.</scope><scope>AAFTH</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>H94</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20090301</creationdate><title>Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor</title><author>Li, Zhenghe ; Pogany, Judit ; Panavas, Tadas ; Xu, Kai ; Esposito, Anthony M ; Kinzy, Terri Goss ; Nagy, Peter D</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c609t-c7d861b92d339e95b95851735f06d8015a51f106eaa7615a4edfb18a23b751333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>3' Untranslated Regions</topic><topic>Brome mosaic virus</topic><topic>Bromovirus - genetics</topic><topic>Bromovirus - physiology</topic><topic>eEF1A</topic><topic>Gene Expression</topic><topic>Host factor</topic><topic>Infectious Disease</topic><topic>Mutation</topic><topic>Peptide Elongation Factor 1 - genetics</topic><topic>Peptide Elongation Factor 1 - metabolism</topic><topic>Protein array</topic><topic>Proteome array</topic><topic>Replicase</topic><topic>Replication</topic><topic>RNA Replicase - genetics</topic><topic>RNA Replicase - metabolism</topic><topic>RNA, Viral - genetics</topic><topic>RNA, Viral - metabolism</topic><topic>Silencer Elements, Transcriptional</topic><topic>TEF1</topic><topic>Tomato bushy stunt virus</topic><topic>Tombusvirus</topic><topic>Tombusvirus - genetics</topic><topic>Tombusvirus - physiology</topic><topic>Ubiquitin-Protein Ligase Complexes - metabolism</topic><topic>Ubiquitination</topic><topic>Viral Proteins - metabolism</topic><topic>Virus Replication - physiology</topic><topic>Yeast as a model host</topic><topic>Yeasts - metabolism</topic><topic>Yeasts - virology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Zhenghe</creatorcontrib><creatorcontrib>Pogany, Judit</creatorcontrib><creatorcontrib>Panavas, Tadas</creatorcontrib><creatorcontrib>Xu, Kai</creatorcontrib><creatorcontrib>Esposito, Anthony M</creatorcontrib><creatorcontrib>Kinzy, Terri Goss</creatorcontrib><creatorcontrib>Nagy, Peter D</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</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>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Virology (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Zhenghe</au><au>Pogany, Judit</au><au>Panavas, Tadas</au><au>Xu, Kai</au><au>Esposito, Anthony M</au><au>Kinzy, Terri Goss</au><au>Nagy, Peter D</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor</atitle><jtitle>Virology (New York, N.Y.)</jtitle><addtitle>Virology</addtitle><date>2009-03-01</date><risdate>2009</risdate><volume>385</volume><issue>1</issue><spage>245</spage><epage>260</epage><pages>245-260</pages><issn>0042-6822</issn><eissn>1096-0341</eissn><abstract>Abstract Host RNA-binding proteins are likely to play multiple, integral roles during replication of plus-strand RNA viruses. To identify host proteins that bind to viral RNAs, we took a global approach based on the yeast proteome microarray, which contains 4080 purified yeast proteins. The biotin-labeled RNA probes included two distantly related RNA viruses, namely Tomato bushy stunt virus (TBSV) and Brome mosaic virus (BMV). Altogether, we have identified 57 yeast proteins that bound to TBSV RNA and/or BMV RNA. Among the identified host proteins, eleven bound to TBSV RNA and seven bound to BMV RNA with high selectivity, whereas the remaining 39 host proteins bound to both viral RNAs. The interaction between the TBSV replicon RNA and five of the identified host proteins was confirmed via gel-mobility shift and co-purification experiments from yeast. Over-expression of the host proteins in yeast, a model host for TBSV, revealed 4 host proteins that enhanced TBSV replication as well as 14 proteins that inhibited replication. Detailed analysis of one of the identified yeast proteins binding to TBSV RNA, namely translation elongation factor eEF1A, revealed that it is present in the highly purified tombusvirus replicase complex. We also demonstrate binding of eEF1A to the p33 replication protein and a known cis-acting element at the 3′ end of TBSV RNA. Using a functional mutant of eEF1A, we provide evidence on the involvement of eEF1A in TBSV replication.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>19131084</pmid><doi>10.1016/j.virol.2008.11.041</doi><tpages>16</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3' Untranslated Regions Brome mosaic virus Bromovirus - genetics Bromovirus - physiology eEF1A Gene Expression Host factor Infectious Disease Mutation Peptide Elongation Factor 1 - genetics Peptide Elongation Factor 1 - metabolism Protein array Proteome array Replicase Replication RNA Replicase - genetics RNA Replicase - metabolism RNA, Viral - genetics RNA, Viral - metabolism Silencer Elements, Transcriptional TEF1 Tomato bushy stunt virus Tombusvirus Tombusvirus - genetics Tombusvirus - physiology Ubiquitin-Protein Ligase Complexes - metabolism Ubiquitination Viral Proteins - metabolism Virus Replication - physiology Yeast as a model host Yeasts - metabolism Yeasts - virology |
title | Translation elongation factor 1A is a component of the tombusvirus replicase complex and affects the stability of the p33 replication co-factor |
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