Translation initiation of viral mRNAs
Identifieur interne : 000F98 ( Istex/Corpus ); précédent : 000F97; suivant : 000F99Translation initiation of viral mRNAs
Auteurs : Marcelo L Pez-Lastra ; Pablo Ramdohr ; Alejandro Letelier ; Maricarmen Vallejos ; Jorge Vera-Otarola ; Fernando Valiente-EcheverríaSource :
- Reviews in Medical Virology [ 1052-9276 ] ; 2010-05.
English descriptors
- Teeft :
- Bicistronic, Biochem, Biochim biophys acta, Biol, Biol chem, Biophys, Cell biol, Cell cycle, Cellular, Cellular mrnas, Cellular proteins, Chem, Codon, Copyright, Eif1, Eif3, Eif4a, Eif4e, Eif4f, Eif4g, Eifs, Embo, Emcv, Encephalomyocarditis virus, Entry site, Eukaryotic, Eukaryotic ribosomes, Eukaryotic translation initiation factor, Helicase, Hellen, Hepatitis, Host cell protein synthesis, Human rhinovirus, Initiation, Initiation codon, Initiation factors, Initiator trna, Internal initiation, Internal ribosome entry site, Internal ribosome entry sites, Ire, Ires activity, Ires elements, Ires factors, Ireses, Itafs, John wiley sons, Leaky scanning, Mrna, Nsp3, Nucleic acids, Pabp, Pestova, Picornavirus, Poliovirus, Protein, Protein synthesis, Reinitiation, Replication, Respiratory syndrome coronavirus, Ribosomal, Ribosomal subunit, Ribosomal subunits, Ribosome, Ribosome entry site, Ribosome shunting, Rna, Sarnow, Shunting, Sonenberg, Subunit, Translation, Translation initiation, Translational, Translational control, Untranslated, Untranslated region, Utrs, Viral, Viral ires, Viral mrna, Viral mrna translation, Viral mrnas, Viral proteins, Virol, Virus.
Abstract
Viruses depend on cells for their replication but have evolved mechanisms to achieve this in an efficient and, in some instances, a cell‐type‐specific manner. The expression of viral proteins is frequently subject to translational control. The dominant target of such control is the initiation step of protein synthesis. Indeed, during the early stages of infection, viral mRNAs must compete with their host counterparts for the protein synthetic machinery, especially for the limited pool of eukaryotic translation initiation factors (eIFs) that mediate the recruitment of ribosomes to both viral and cellular mRNAs. To circumvent this competition viruses use diverse strategies so that ribosomes can be recruited selectively to viral mRNAs. In this review we focus on the initiation of protein synthesis and outline some of the strategies used by viruses to ensure efficient translation initiation of their mRNAs. Copyright © 2010 John Wiley & Sons, Ltd.
Url:
DOI: 10.1002/rmv.649
Links to Exploration step
ISTEX:FA82ACC43D89E3B29F42BFE0780C0178E80FD4E4Le document en format XML
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Alejandro" sort="Letelier, Alejandro" uniqKey="Letelier A" first="Alejandro" last="Letelier">Alejandro Letelier</name><affiliation><mods:affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</mods:affiliation></affiliation></author><author><name sortKey="Vallejos, Maricarmen" sort="Vallejos, Maricarmen" uniqKey="Vallejos M" first="Maricarmen" last="Vallejos">Maricarmen Vallejos</name><affiliation><mods:affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</mods:affiliation></affiliation></author><author><name sortKey="Vera Tarola, Jorge" sort="Vera Tarola, Jorge" uniqKey="Vera Tarola J" first="Jorge" last="Vera-Otarola">Jorge Vera-Otarola</name><affiliation><mods:affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</mods:affiliation></affiliation></author><author><name sortKey="Valiente Cheverria, Fernando" sort="Valiente Cheverria, Fernando" uniqKey="Valiente Cheverria F" first="Fernando" last="Valiente-Echeverría">Fernando Valiente-Echeverría</name><affiliation><mods:affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</mods:affiliation></affiliation></author></analytic><monogr></monogr><series><title level="j" type="main">Reviews in Medical Virology</title><title level="j" type="alt">REVIEWS IN MEDICAL VIROLOGY</title><idno type="ISSN">1052-9276</idno><idno type="eISSN">1099-1654</idno><imprint><biblScope unit="vol">20</biblScope><biblScope unit="issue">3</biblScope><biblScope unit="page" from="177">177</biblScope><biblScope unit="page" to="195">195</biblScope><biblScope unit="page-count">19</biblScope><publisher>John Wiley & Sons, Ltd.</publisher><pubPlace>Chichester, UK</pubPlace><date type="published" when="2010-05">2010-05</date></imprint><idno type="ISSN">1052-9276</idno></series></biblStruct></sourceDesc><seriesStmt><idno type="ISSN">1052-9276</idno></seriesStmt></fileDesc><profileDesc><textClass><keywords scheme="Teeft" xml:lang="en"><term>Bicistronic</term><term>Biochem</term><term>Biochim biophys acta</term><term>Biol</term><term>Biol chem</term><term>Biophys</term><term>Cell biol</term><term>Cell cycle</term><term>Cellular</term><term>Cellular mrnas</term><term>Cellular proteins</term><term>Chem</term><term>Codon</term><term>Copyright</term><term>Eif1</term><term>Eif3</term><term>Eif4a</term><term>Eif4e</term><term>Eif4f</term><term>Eif4g</term><term>Eifs</term><term>Embo</term><term>Emcv</term><term>Encephalomyocarditis virus</term><term>Entry site</term><term>Eukaryotic</term><term>Eukaryotic ribosomes</term><term>Eukaryotic translation initiation factor</term><term>Helicase</term><term>Hellen</term><term>Hepatitis</term><term>Host cell protein synthesis</term><term>Human rhinovirus</term><term>Initiation</term><term>Initiation codon</term><term>Initiation factors</term><term>Initiator trna</term><term>Internal initiation</term><term>Internal ribosome entry site</term><term>Internal ribosome entry sites</term><term>Ire</term><term>Ires activity</term><term>Ires elements</term><term>Ires factors</term><term>Ireses</term><term>Itafs</term><term>John wiley sons</term><term>Leaky scanning</term><term>Mrna</term><term>Nsp3</term><term>Nucleic acids</term><term>Pabp</term><term>Pestova</term><term>Picornavirus</term><term>Poliovirus</term><term>Protein</term><term>Protein synthesis</term><term>Reinitiation</term><term>Replication</term><term>Respiratory syndrome coronavirus</term><term>Ribosomal</term><term>Ribosomal subunit</term><term>Ribosomal subunits</term><term>Ribosome</term><term>Ribosome entry site</term><term>Ribosome shunting</term><term>Rna</term><term>Sarnow</term><term>Shunting</term><term>Sonenberg</term><term>Subunit</term><term>Translation</term><term>Translation initiation</term><term>Translational</term><term>Translational control</term><term>Untranslated</term><term>Untranslated region</term><term>Utrs</term><term>Viral</term><term>Viral ires</term><term>Viral mrna</term><term>Viral mrna translation</term><term>Viral mrnas</term><term>Viral proteins</term><term>Virol</term><term>Virus</term></keywords></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en">Viruses depend on cells for their replication but have evolved mechanisms to achieve this in an efficient and, in some instances, a cell‐type‐specific manner. The expression of viral proteins is frequently subject to translational control. The dominant target of such control is the initiation step of protein synthesis. Indeed, during the early stages of infection, viral mRNAs must compete with their host counterparts for the protein synthetic machinery, especially for the limited pool of eukaryotic translation initiation factors (eIFs) that mediate the recruitment of ribosomes to both viral and cellular mRNAs. To circumvent this competition viruses use diverse strategies so that ribosomes can be recruited selectively to viral mRNAs. In this review we focus on the initiation of protein synthesis and outline some of the strategies used by viruses to ensure efficient translation initiation of their mRNAs. Copyright © 2010 John Wiley & Sons, Ltd.</div></front></TEI><istex><corpusName>wiley</corpusName><keywords><teeft><json:string>mrna</json:string><json:string>viral</json:string><json:string>ribosome</json:string><json:string>virol</json:string><json:string>translation initiation</json:string><json:string>ire</json:string><json:string>ribosomal</json:string><json:string>eif4g</json:string><json:string>subunit</json:string><json:string>codon</json:string><json:string>biol</json:string><json:string>eukaryotic</json:string><json:string>translational</json:string><json:string>viral mrnas</json:string><json:string>ireses</json:string><json:string>eif4e</json:string><json:string>eif4f</json:string><json:string>john wiley sons</json:string><json:string>pabp</json:string><json:string>copyright</json:string><json:string>protein synthesis</json:string><json:string>viral mrna</json:string><json:string>ribosomal 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activity</json:string><json:string>gene expression</json:string><json:string>satellite tobacco necrosis virus</json:string><json:string>human virus type</json:string><json:string>virus replication</json:string><json:string>disease virus</json:string><json:string>picornavirus ireses</json:string><json:string>binding protein</json:string><json:string>untranslated regions</json:string><json:string>binding sites</json:string><json:string>initiation codons</json:string><json:string>mrna translation</json:string></teeft></keywords><author><json:item><name>Marcelo López‐Lastra</name><affiliations><json:string>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</json:string><json:string>E-mail: malopez@med.puc.cl</json:string><json:string>Correspondence address: Laboratorio de Virología Molecular, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile.</json:string></affiliations></json:item><json:item><name>Pablo Ramdohr</name><affiliations><json:string>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</json:string></affiliations></json:item><json:item><name>Alejandro Letelier</name><affiliations><json:string>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</json:string></affiliations></json:item><json:item><name>Maricarmen Vallejos</name><affiliations><json:string>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</json:string></affiliations></json:item><json:item><name>Jorge Vera‐Otarola</name><affiliations><json:string>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</json:string></affiliations></json:item><json:item><name>Fernando Valiente‐Echeverría</name><affiliations><json:string>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</json:string></affiliations></json:item></author><articleId><json:string>RMV649</json:string></articleId><arkIstex>ark:/67375/WNG-N1CLFBWG-C</arkIstex><language><json:string>eng</json:string></language><originalGenre><json:string>reviewArticle</json:string></originalGenre><abstract>Viruses depend on cells for their replication but have evolved mechanisms to achieve this in an efficient and, in some instances, a cell‐type‐specific manner. The expression of viral proteins is frequently subject to translational control. The dominant target of such control is the initiation step of protein synthesis. Indeed, during the early stages of infection, viral mRNAs must compete with their host counterparts for the protein synthetic machinery, especially for the limited pool of eukaryotic translation initiation factors (eIFs) that mediate the recruitment of ribosomes to both viral and cellular mRNAs. To circumvent this competition viruses use diverse strategies so that ribosomes can be recruited selectively to viral mRNAs. In this review we focus on the initiation of protein synthesis and outline some of the strategies used by viruses to ensure efficient translation initiation of their mRNAs. Copyright © 2010 John Wiley & Sons, Ltd.</abstract><qualityIndicators><score>8.74</score><pdfWordCount>11078</pdfWordCount><pdfCharCount>72209</pdfCharCount><pdfVersion>1.3</pdfVersion><pdfPageCount>19</pdfPageCount><pdfPageSize>574 x 741 pts</pdfPageSize><pdfWordsPerPage>583</pdfWordsPerPage><pdfText>true</pdfText><refBibsNative>true</refBibsNative><abstractWordCount>145</abstractWordCount><abstractCharCount>956</abstractCharCount><keywordCount>0</keywordCount></qualityIndicators><title>Translation initiation of viral mRNAs</title><pmid><json:string>20440748</json:string></pmid><genre><json:string>review-article</json:string></genre><host><title>Reviews in Medical Virology</title><language><json:string>unknown</json:string></language><doi><json:string>10.1002/(ISSN)1099-1654</json:string></doi><issn><json:string>1052-9276</json:string></issn><eissn><json:string>1099-1654</json:string></eissn><publisherId><json:string>RMV</json:string></publisherId><volume>20</volume><issue>3</issue><pages><first>177</first><last>195</last><total>19</total></pages><genre><json:string>journal</json:string></genre><subject><json:item><value>Review</value></json:item><json:item><value>Reviews</value></json:item></subject></host><namedEntities><unitex><date><json:string>40S</json:string><json:string>48S</json:string><json:string>80S</json:string><json:string>18S</json:string><json:string>43S</json:string><json:string>35S</json:string><json:string>60S</json:string><json:string>2010</json:string></date><geogName></geogName><orgName><json:string>Sons, Ltd.</json:string><json:string>Chile SUMMARY Viruses</json:string><json:string>Chile, Marcoleta</json:string><json:string>Sons, Ltd</json:string></orgName><orgName_funder></orgName_funder><orgName_provider></orgName_provider><persName><json:string>M. 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Copyright © 2010 John Wiley & Sons, Ltd.</p></abstract></abstractGroup></contentMeta></header></component></istex:document></istex:metadataXml><mods version="3.6"><titleInfo lang="en"><title>Translation initiation of viral mRNAs</title></titleInfo><titleInfo type="abbreviated" lang="en"><title>Translation initiation of viral mRNAs</title></titleInfo><titleInfo type="alternative" contentType="CDATA" lang="en"><title>Translation initiation of viral mRNAs</title></titleInfo><name type="personal"><namePart type="given">Marcelo</namePart><namePart type="family">López‐Lastra</namePart><affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</affiliation><affiliation>E-mail: malopez@med.puc.cl</affiliation><affiliation>Correspondence address: Laboratorio de Virología Molecular, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile.</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Pablo</namePart><namePart type="family">Ramdohr</namePart><affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Alejandro</namePart><namePart type="family">Letelier</namePart><affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Maricarmen</namePart><namePart type="family">Vallejos</namePart><affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Jorge</namePart><namePart type="family">Vera‐Otarola</namePart><affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</affiliation><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">Fernando</namePart><namePart type="family">Valiente‐Echeverría</namePart><affiliation>Laboratorio de Virología Molecular, Instituto Milenio de Inmunología e Inmunoterapia, Centro de Investigaciones Médicas, Facultad de Medicina, Pontificia Universidad Católica de Chile, Marcoleta 391, Santiago, Chile</affiliation><role><roleTerm type="text">author</roleTerm></role></name><typeOfResource>text</typeOfResource><genre type="review-article" displayLabel="reviewArticle" authority="ISTEX" authorityURI="https://content-type.data.istex.fr" valueURI="https://content-type.data.istex.fr/ark:/67375/XTP-L5L7X3NF-P">review-article</genre><originInfo><publisher>John Wiley & Sons, Ltd.</publisher><place><placeTerm type="text">Chichester, UK</placeTerm></place><dateIssued encoding="w3cdtf">2010-05</dateIssued><dateCaptured encoding="w3cdtf">2009-10-29</dateCaptured><dateValid encoding="w3cdtf">2010-01-18</dateValid><copyrightDate encoding="w3cdtf">2010</copyrightDate></originInfo><language><languageTerm type="code" authority="rfc3066">en</languageTerm><languageTerm type="code" authority="iso639-2b">eng</languageTerm></language><physicalDescription><extent unit="figures">3</extent><extent unit="tables">0</extent><extent unit="references">167</extent></physicalDescription><abstract lang="en">Viruses depend on cells for their replication but have evolved mechanisms to achieve this in an efficient and, in some instances, a cell‐type‐specific manner. The expression of viral proteins is frequently subject to translational control. The dominant target of such control is the initiation step of protein synthesis. Indeed, during the early stages of infection, viral mRNAs must compete with their host counterparts for the protein synthetic machinery, especially for the limited pool of eukaryotic translation initiation factors (eIFs) that mediate the recruitment of ribosomes to both viral and cellular mRNAs. To circumvent this competition viruses use diverse strategies so that ribosomes can be recruited selectively to viral mRNAs. In this review we focus on the initiation of protein synthesis and outline some of the strategies used by viruses to ensure efficient translation initiation of their mRNAs. Copyright © 2010 John Wiley & Sons, Ltd.</abstract><relatedItem type="host"><titleInfo><title>Reviews in Medical Virology</title></titleInfo><titleInfo type="abbreviated"><title>Rev. Med. Virol.</title></titleInfo><genre type="journal" authority="ISTEX" authorityURI="https://publication-type.data.istex.fr" valueURI="https://publication-type.data.istex.fr/ark:/67375/JMC-0GLKJH51-B">journal</genre><subject><genre>article-category</genre><topic>Review</topic><topic>Reviews</topic></subject><identifier type="ISSN">1052-9276</identifier><identifier type="eISSN">1099-1654</identifier><identifier type="DOI">10.1002/(ISSN)1099-1654</identifier><identifier type="PublisherID">RMV</identifier><part><date>2010</date><detail type="volume"><caption>vol.</caption><number>20</number></detail><detail type="issue"><caption>no.</caption><number>3</number></detail><extent unit="pages"><start>177</start><end>195</end><total>19</total></extent></part></relatedItem><relatedItem type="references" displayLabel="cit1"><titleInfo><title>Regulation of translation initiation in eukaryotes: mechanisms and biological targets</title></titleInfo><name type="personal"><namePart type="given">N</namePart><namePart type="family">Sonenberg</namePart><role><roleTerm type="text">author</roleTerm></role></name><name type="personal"><namePart type="given">AG</namePart><namePart type="family">Hinnebusch</namePart><role><roleTerm type="text">author</roleTerm></role></name><genre>journal-article</genre><note type="citation/reference">Sonenberg N, Hinnebusch AG. 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