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Annotation of long non-coding RNAs expressed in collaborative cross founder mice in response to respiratory virus infection reveals a new class of interferon-stimulated transcripts.

Identifieur interne : 001706 ( Main/Exploration ); précédent : 001705; suivant : 001707

Annotation of long non-coding RNAs expressed in collaborative cross founder mice in response to respiratory virus infection reveals a new class of interferon-stimulated transcripts.

Auteurs : Laurence Josset [États-Unis] ; Nicolas Tchitchek [États-Unis] ; Lisa E. Gralinski [États-Unis] ; Martin T. Ferris [États-Unis] ; Amie J. Eisfeld [États-Unis] ; Richard R. Green [États-Unis] ; Matthew J. Thomas [États-Unis] ; Jennifer Tisoncik-Go [États-Unis] ; Gary P. Schroth [États-Unis] ; Yoshihiro Kawaoka [États-Unis] ; Fernando Pardo Manuel De Villena [États-Unis] ; Ralph S. Baric [États-Unis] ; Mark T. Heise [États-Unis] ; Xinxia Peng [États-Unis] ; Michael G. Katze [États-Unis]

Source :

RBID : pubmed:24922324

Descripteurs français

English descriptors

Abstract

The outcome of respiratory virus infection is determined by a complex interplay of viral and host factors. Some potentially important host factors for the antiviral response, whose functions remain largely unexplored, are long non-coding RNAs (lncRNAs). Here we systematically inferred the regulatory functions of host lncRNAs in response to influenza A virus and severe acute respiratory syndrome coronavirus (SARS-CoV) based on their similarity in expression with genes of known function. We performed total RNA-Seq on viral-infected lungs from eight mouse strains, yielding a large data set of transcriptional responses. Overall 5,329 lncRNAs were differentially expressed after infection. Most of the lncRNAs were co-expressed with coding genes in modules enriched in genes associated with lung homeostasis pathways or immune response processes. Each lncRNA was further individually annotated using a rank-based method, enabling us to associate 5,295 lncRNAs to at least one gene set and to predict their potential cis effects. We validated the lncRNAs predicted to be interferon-stimulated by profiling mouse responses after interferon-α treatment. Altogether, these results provide a broad categorization of potential lncRNA functions and identify subsets of lncRNAs with likely key roles in respiratory virus pathogenesis. These data are fully accessible through the MOuse NOn-Code Lung interactive database (MONOCLdb).

DOI: 10.4161/rna.29442
PubMed: 24922324


Affiliations:


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<wicri:cityArea>Department of Pathobiological Sciences; Influenza Research Institute; University of Wisconsin-Madison; Madison</wicri:cityArea>
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<name sortKey="Manuel De Villena, Fernando Pardo" sort="Manuel De Villena, Fernando Pardo" uniqKey="Manuel De Villena F" first="Fernando Pardo" last="Manuel De Villena">Fernando Pardo Manuel De Villena</name>
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<region type="state">Caroline du Nord</region>
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<country>États-Unis</country>
<placeName>
<region type="state">Oregon</region>
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<wicri:cityArea>Department of Microbiology; School of Medicine; University of Washington; Seattle, WA USA; Pacific Northwest Regional Center of Excellence for Biodefense and Emerging Infectious Diseases Research; Portland</wicri:cityArea>
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<name sortKey="Katze, Michael G" sort="Katze, Michael G" uniqKey="Katze M" first="Michael G" last="Katze">Michael G. Katze</name>
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<region type="state">Oregon</region>
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<term>Antiviral Agents (pharmacology)</term>
<term>Cell Line</term>
<term>Female</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation (drug effects)</term>
<term>Influenza A virus (drug effects)</term>
<term>Influenza A virus (physiology)</term>
<term>Interferon-alpha (administration & dosage)</term>
<term>Interferon-alpha (pharmacology)</term>
<term>Lung (metabolism)</term>
<term>Lung (virology)</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Molecular Sequence Annotation</term>
<term>RNA Virus Infections (drug therapy)</term>
<term>RNA Virus Infections (genetics)</term>
<term>RNA Virus Infections (virology)</term>
<term>RNA, Long Noncoding (genetics)</term>
<term>SARS Virus (drug effects)</term>
<term>SARS Virus (physiology)</term>
<term>Sequence Analysis, RNA</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>ARN long non codant (génétique)</term>
<term>Analyse de profil d'expression de gènes</term>
<term>Analyse de séquence d'ARN</term>
<term>Animaux</term>
<term>Annotation de séquence moléculaire</term>
<term>Antiviraux (administration et posologie)</term>
<term>Antiviraux (pharmacologie)</term>
<term>Femelle</term>
<term>Infections à virus à ARN (génétique)</term>
<term>Infections à virus à ARN (traitement médicamenteux)</term>
<term>Infections à virus à ARN (virologie)</term>
<term>Interféron alpha (administration et posologie)</term>
<term>Interféron alpha (pharmacologie)</term>
<term>Lignée cellulaire</term>
<term>Poumon (métabolisme)</term>
<term>Poumon (virologie)</term>
<term>Régulation de l'expression des gènes ()</term>
<term>Souris</term>
<term>Souris de lignée C57BL</term>
<term>Virus de la grippe A ()</term>
<term>Virus de la grippe A (physiologie)</term>
<term>Virus du SRAS ()</term>
<term>Virus du SRAS (physiologie)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="administration & dosage" xml:lang="en">
<term>Antiviral Agents</term>
<term>Interferon-alpha</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>RNA, Long Noncoding</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="pharmacology" xml:lang="en">
<term>Antiviral Agents</term>
<term>Interferon-alpha</term>
</keywords>
<keywords scheme="MESH" qualifier="administration et posologie" xml:lang="fr">
<term>Antiviraux</term>
<term>Interféron alpha</term>
</keywords>
<keywords scheme="MESH" qualifier="drug effects" xml:lang="en">
<term>Gene Expression Regulation</term>
<term>Influenza A virus</term>
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="drug therapy" xml:lang="en">
<term>RNA Virus Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>RNA Virus Infections</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>ARN long non codant</term>
<term>Infections à virus à ARN</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>Lung</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Poumon</term>
</keywords>
<keywords scheme="MESH" qualifier="pharmacologie" xml:lang="fr">
<term>Antiviraux</term>
<term>Interféron alpha</term>
</keywords>
<keywords scheme="MESH" qualifier="physiologie" xml:lang="fr">
<term>Virus de la grippe A</term>
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="physiology" xml:lang="en">
<term>Influenza A virus</term>
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="traitement médicamenteux" xml:lang="fr">
<term>Infections à virus à ARN</term>
</keywords>
<keywords scheme="MESH" qualifier="virologie" xml:lang="fr">
<term>Infections à virus à ARN</term>
<term>Poumon</term>
</keywords>
<keywords scheme="MESH" qualifier="virology" xml:lang="en">
<term>Lung</term>
<term>RNA Virus Infections</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Cell Line</term>
<term>Female</term>
<term>Gene Expression Profiling</term>
<term>Mice</term>
<term>Mice, Inbred C57BL</term>
<term>Molecular Sequence Annotation</term>
<term>Sequence Analysis, RNA</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse de profil d'expression de gènes</term>
<term>Analyse de séquence d'ARN</term>
<term>Animaux</term>
<term>Annotation de séquence moléculaire</term>
<term>Femelle</term>
<term>Lignée cellulaire</term>
<term>Régulation de l'expression des gènes</term>
<term>Souris</term>
<term>Souris de lignée C57BL</term>
<term>Virus de la grippe A</term>
<term>Virus du SRAS</term>
</keywords>
</textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">The outcome of respiratory virus infection is determined by a complex interplay of viral and host factors. Some potentially important host factors for the antiviral response, whose functions remain largely unexplored, are long non-coding RNAs (lncRNAs). Here we systematically inferred the regulatory functions of host lncRNAs in response to influenza A virus and severe acute respiratory syndrome coronavirus (SARS-CoV) based on their similarity in expression with genes of known function. We performed total RNA-Seq on viral-infected lungs from eight mouse strains, yielding a large data set of transcriptional responses. Overall 5,329 lncRNAs were differentially expressed after infection. Most of the lncRNAs were co-expressed with coding genes in modules enriched in genes associated with lung homeostasis pathways or immune response processes. Each lncRNA was further individually annotated using a rank-based method, enabling us to associate 5,295 lncRNAs to at least one gene set and to predict their potential cis effects. We validated the lncRNAs predicted to be interferon-stimulated by profiling mouse responses after interferon-α treatment. Altogether, these results provide a broad categorization of potential lncRNA functions and identify subsets of lncRNAs with likely key roles in respiratory virus pathogenesis. These data are fully accessible through the MOuse NOn-Code Lung interactive database (MONOCLdb). </div>
</front>
</TEI>
<affiliations>
<list>
<country>
<li>États-Unis</li>
</country>
<region>
<li>Californie</li>
<li>Caroline du Nord</li>
<li>Oregon</li>
<li>Wisconsin</li>
</region>
<settlement>
<li>Madison (Wisconsin)</li>
</settlement>
<orgName>
<li>Université du Wisconsin à Madison</li>
</orgName>
</list>
<tree>
<country name="États-Unis">
<region name="Oregon">
<name sortKey="Josset, Laurence" sort="Josset, Laurence" uniqKey="Josset L" first="Laurence" last="Josset">Laurence Josset</name>
</region>
<name sortKey="Baric, Ralph S" sort="Baric, Ralph S" uniqKey="Baric R" first="Ralph S" last="Baric">Ralph S. Baric</name>
<name sortKey="Eisfeld, Amie J" sort="Eisfeld, Amie J" uniqKey="Eisfeld A" first="Amie J" last="Eisfeld">Amie J. Eisfeld</name>
<name sortKey="Ferris, Martin T" sort="Ferris, Martin T" uniqKey="Ferris M" first="Martin T" last="Ferris">Martin T. Ferris</name>
<name sortKey="Gralinski, Lisa E" sort="Gralinski, Lisa E" uniqKey="Gralinski L" first="Lisa E" last="Gralinski">Lisa E. Gralinski</name>
<name sortKey="Green, Richard R" sort="Green, Richard R" uniqKey="Green R" first="Richard R" last="Green">Richard R. Green</name>
<name sortKey="Heise, Mark T" sort="Heise, Mark T" uniqKey="Heise M" first="Mark T" last="Heise">Mark T. Heise</name>
<name sortKey="Katze, Michael G" sort="Katze, Michael G" uniqKey="Katze M" first="Michael G" last="Katze">Michael G. Katze</name>
<name sortKey="Kawaoka, Yoshihiro" sort="Kawaoka, Yoshihiro" uniqKey="Kawaoka Y" first="Yoshihiro" last="Kawaoka">Yoshihiro Kawaoka</name>
<name sortKey="Manuel De Villena, Fernando Pardo" sort="Manuel De Villena, Fernando Pardo" uniqKey="Manuel De Villena F" first="Fernando Pardo" last="Manuel De Villena">Fernando Pardo Manuel De Villena</name>
<name sortKey="Peng, Xinxia" sort="Peng, Xinxia" uniqKey="Peng X" first="Xinxia" last="Peng">Xinxia Peng</name>
<name sortKey="Schroth, Gary P" sort="Schroth, Gary P" uniqKey="Schroth G" first="Gary P" last="Schroth">Gary P. Schroth</name>
<name sortKey="Tchitchek, Nicolas" sort="Tchitchek, Nicolas" uniqKey="Tchitchek N" first="Nicolas" last="Tchitchek">Nicolas Tchitchek</name>
<name sortKey="Thomas, Matthew J" sort="Thomas, Matthew J" uniqKey="Thomas M" first="Matthew J" last="Thomas">Matthew J. Thomas</name>
<name sortKey="Tisoncik Go, Jennifer" sort="Tisoncik Go, Jennifer" uniqKey="Tisoncik Go J" first="Jennifer" last="Tisoncik-Go">Jennifer Tisoncik-Go</name>
</country>
</tree>
</affiliations>
</record>

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