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The role of RNA folding free energy in the evolution of the polymerase genes of the influenza A virus

Identifieur interne : 000984 ( Pmc/Checkpoint ); précédent : 000983; suivant : 000985

The role of RNA folding free energy in the evolution of the polymerase genes of the influenza A virus

Auteurs : Rachel Brower-Sinning [États-Unis] ; Donald M. Carter [États-Unis] ; Corey J. Crevar [États-Unis] ; Elodie Ghedin [États-Unis] ; Ted M. Ross [États-Unis] ; Panayiotis V. Benos [États-Unis]

Source :

RBID : PMC:2688270

Abstract

RNA folding free energy is important for the evolution and host-adaptation of the influenza virus. Human virus polymerase genes are shown to have substantially higher folding free energy values than their avian counterparts.


Url:
DOI: 10.1186/gb-2009-10-2-r18
PubMed: 19216739
PubMed Central: 2688270


Affiliations:


Links toward previous steps (curation, corpus...)


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PMC:2688270

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<article-title>The role of RNA folding free energy in the evolution of the polymerase genes of the influenza A virus</article-title>
</title-group>
<contrib-group>
<contrib id="A1" contrib-type="author">
<name>
<surname>Brower-Sinning</surname>
<given-names>Rachel</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<email>rab71@pitt.edu</email>
</contrib>
<contrib id="A2" contrib-type="author">
<name>
<surname>Carter</surname>
<given-names>Donald M</given-names>
</name>
<xref ref-type="aff" rid="I2">2</xref>
<email>dmc46@cvr.pitt.edu</email>
</contrib>
<contrib id="A3" contrib-type="author">
<name>
<surname>Crevar</surname>
<given-names>Corey J</given-names>
</name>
<xref ref-type="aff" rid="I2">2</xref>
<email>cjc63@cvr.pitt.edu</email>
</contrib>
<contrib id="A4" contrib-type="author">
<name>
<surname>Ghedin</surname>
<given-names>Elodie</given-names>
</name>
<xref ref-type="aff" rid="I3">3</xref>
<email>elg21@pitt.edu</email>
</contrib>
<contrib id="A5" contrib-type="author">
<name>
<surname>Ross</surname>
<given-names>Ted M</given-names>
</name>
<xref ref-type="aff" rid="I2">2</xref>
<xref ref-type="aff" rid="I4">4</xref>
<email>tmr15@cvr.pitt.edu</email>
</contrib>
<contrib id="A6" corresp="yes" contrib-type="author">
<name>
<surname>Benos</surname>
<given-names>Panayiotis V</given-names>
</name>
<xref ref-type="aff" rid="I1">1</xref>
<xref ref-type="aff" rid="I5">5</xref>
<email>benos@pitt.edu</email>
</contrib>
</contrib-group>
<aff id="I1">
<label>1</label>
Department of Computational Biology, School of Medicine, University of Pittsburgh, Fifth Avenue, Pittsburgh, PA 15260, USA</aff>
<aff id="I2">
<label>2</label>
Center for Vaccine Research, University of Pittsburgh, Fifth Avenue, Pittsburgh, PA 15260, USA</aff>
<aff id="I3">
<label>3</label>
Department of Medicine, School of Medicine, University of Pittsburgh, Fifth Avenue, Pittsburgh, PA 15261, USA</aff>
<aff id="I4">
<label>4</label>
Department of Microbiology and Molecular Genetics, School of Medicine, University of Pittsburgh, Lothrop Street, Pittsburgh, PA 15261, USA</aff>
<aff id="I5">
<label>5</label>
Department of Biomedical Informatics, School of Medicine, University of Pittsburgh, Meyran Avenue, Pittsburgh, PA 15260, USA</aff>
<pub-date pub-type="ppub">
<year>2009</year>
</pub-date>
<pub-date pub-type="epub">
<day>12</day>
<month>2</month>
<year>2009</year>
</pub-date>
<volume>10</volume>
<issue>2</issue>
<fpage>R18</fpage>
<lpage>R18</lpage>
<ext-link ext-link-type="uri" xlink:href="http://genomebiology.com/2009/10/2/R18"></ext-link>
<history>
<date date-type="received">
<day>4</day>
<month>12</month>
<year>2008</year>
</date>
<date date-type="rev-recd">
<day>29</day>
<month>1</month>
<year>2009</year>
</date>
<date date-type="accepted">
<day>12</day>
<month>2</month>
<year>2009</year>
</date>
</history>
<permissions>
<copyright-statement>Copyright © 2009 Brower-Sinning et al.; licensee BioMed Central Ltd.</copyright-statement>
<copyright-year>2009</copyright-year>
<copyright-holder>Brower-Sinning et al.; licensee BioMed Central Ltd.</copyright-holder>
<license license-type="open-access" xlink:href="http://creativecommons.org/licenses/by/2.0">
<p>This is an open access article distributed under the terms of the Creative Commons Attribution License (
<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by/2.0"></ext-link>
), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</p>
<pmc-comment> Brower-Sinning Rachel rab71@pitt.edu The role of RNA folding free energy in the evolution of the polymerase genes of the influenza A virus 2009Genome Biology 10(2): R18-. (2009)1465-6906(2009)10:2urn:ISSN:1465-6906</pmc-comment>
</license>
</permissions>
<abstract abstract-type="short">
<p>RNA folding free energy is important for the evolution and host-adaptation of the influenza virus. Human virus polymerase genes are shown to have substantially higher folding free energy values than their avian counterparts.</p>
</abstract>
<abstract>
<sec>
<title>Background</title>
<p>The influenza A virus genome is composed of eight single-stranded RNA segments of negative polarity. Although the hemagglutinin and neuraminidase genes are known to play a key role in host adaptation, the polymerase genes (which encode the polymerase segments PB2, PB1, PA) and the nucleoprotein gene are also important for the efficient propagation of the virus in the host and for its adaptation to new hosts. Current efforts to understand the host-specificity of the virus have largely focused on the amino acid differences between avian and human isolates.</p>
</sec>
<sec>
<title>Results</title>
<p>Here we show that the folding free energy of the RNA segments may play an equally important role in the evolution and host adaptation of the influenza virus. Folding free energy may affect the stability of the viral RNA and influence the rate of viral protein translation. We found that there is a clear distinction between the avian and human folding free energy distributions for the polymerase and the nucleoprotein genes, with human viruses having substantially higher folding free energy values. This difference is independent of the amino acid composition and the codon bias. Furthermore, the folding free energy values of the commonly circulating human viruses tend to shift towards higher values over the years, after they entered the human population. Finally, our results indicate that the temperature in which the cells grow affects infection efficiency.</p>
</sec>
<sec>
<title>Conclusions</title>
<p>Our data suggest for the first time that RNA structure stability may play an important role in the emergence and host shift of influenza A virus. The fact that cell temperature affects virus propagation in mammalian cells could help identify those avian strains that pose a higher threat to humans.</p>
</sec>
</abstract>
</article-meta>
</front>
</pmc>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Pennsylvanie</li>
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   |type=    RBID
   |clé=     PMC:2688270
   |texte=   The role of RNA folding free energy in the evolution of the polymerase genes of the influenza A virus
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Checkpoint/RBID.i   -Sk "pubmed:19216739" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Checkpoint/biblio.hfd   \
       | NlmPubMed2Wicri -a H2N2V1 

Wicri

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