Unique signatures of long noncoding RNA expression in response to virus infection and altered innate immune signaling.
Identifieur interne : 002239 ( Ncbi/Curation ); précédent : 002238; suivant : 002240Unique signatures of long noncoding RNA expression in response to virus infection and altered innate immune signaling.
Auteurs : Xinxia Peng [États-Unis] ; Lisa Gralinski ; Christopher D. Armour ; Martin T. Ferris ; Matthew J. Thomas ; Sean Proll ; Birgit G. Bradel-Tretheway ; Marcus J. Korth ; John C. Castle ; Matthew C. Biery ; Heather K. Bouzek ; David R. Haynor ; Matthew B. Frieman ; Mark Heise ; Christopher K. Raymond ; Ralph S. Baric ; Michael G. KatzeSource :
- mBio [ 2150-7511 ] ; 2010.
Descripteurs français
- KwdFr :
- ARN non traduit (biosynthèse), Analyse de profil d'expression de gènes, Animaux, Immunité innée, Modèles animaux de maladie humaine, Régulation de l'expression des gènes, Souris, Syndrome respiratoire aigu sévère (anatomopathologie), Syndrome respiratoire aigu sévère (immunologie), Syndrome respiratoire aigu sévère (virologie), Transcription génétique, Transduction du signal, Virus du SRAS (immunologie), Virus du SRAS (pathogénicité).
- MESH :
- anatomopathologie : Syndrome respiratoire aigu sévère.
- biosynthèse : ARN non traduit.
- immunologie : Syndrome respiratoire aigu sévère, Virus du SRAS.
- pathogénicité : Virus du SRAS.
- virologie : Syndrome respiratoire aigu sévère.
- Analyse de profil d'expression de gènes, Animaux, Immunité innée, Modèles animaux de maladie humaine, Régulation de l'expression des gènes, Souris, Transcription génétique, Transduction du signal.
English descriptors
- KwdEn :
- Animals, Disease Models, Animal, Gene Expression Profiling, Gene Expression Regulation, Immunity, Innate, Mice, RNA, Untranslated (biosynthesis), SARS Virus (immunology), SARS Virus (pathogenicity), Severe Acute Respiratory Syndrome (immunology), Severe Acute Respiratory Syndrome (pathology), Severe Acute Respiratory Syndrome (virology), Signal Transduction, Transcription, Genetic.
- MESH :
- chemical , biosynthesis : RNA, Untranslated.
- immunology : SARS Virus, Severe Acute Respiratory Syndrome.
- pathogenicity : SARS Virus.
- pathology : Severe Acute Respiratory Syndrome.
- virology : Severe Acute Respiratory Syndrome.
- Animals, Disease Models, Animal, Gene Expression Profiling, Gene Expression Regulation, Immunity, Innate, Mice, Signal Transduction, Transcription, Genetic.
Abstract
Studies of the host response to virus infection typically focus on protein-coding genes. However, non-protein-coding RNAs (ncRNAs) are transcribed in mammalian cells, and the roles of many of these ncRNAs remain enigmas. Using next-generation sequencing, we performed a whole-transcriptome analysis of the host response to severe acute respiratory syndrome coronavirus (SARS-CoV) infection across four founder mouse strains of the Collaborative Cross. We observed differential expression of approximately 500 annotated, long ncRNAs and 1,000 nonannotated genomic regions during infection. Moreover, studies of a subset of these ncRNAs and genomic regions showed the following. (i) Most were similarly regulated in response to influenza virus infection. (ii) They had distinctive kinetic expression profiles in type I interferon receptor and STAT1 knockout mice during SARS-CoV infection, including unique signatures of ncRNA expression associated with lethal infection. (iii) Over 40% were similarly regulated in vitro in response to both influenza virus infection and interferon treatment. These findings represent the first discovery of the widespread differential expression of long ncRNAs in response to virus infection and suggest that ncRNAs are involved in regulating the host response, including innate immunity. At the same time, virus infection models provide a unique platform for studying the biology and regulation of ncRNAs.
DOI: 10.1128/mBio.00206-10
PubMed: 20978541
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pubmed:20978541Le document en format XML
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<affiliation wicri:level="4"><nlm:affiliation>Department of Microbiology, School of Medicine, University of Washington, Seattle, Washington, USA.</nlm:affiliation>
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<term>Gene Expression Regulation</term>
<term>Immunity, Innate</term>
<term>Mice</term>
<term>RNA, Untranslated (biosynthesis)</term>
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<term>SARS Virus (pathogenicity)</term>
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<term>Animaux</term>
<term>Immunité innée</term>
<term>Modèles animaux de maladie humaine</term>
<term>Régulation de l'expression des gènes</term>
<term>Souris</term>
<term>Syndrome respiratoire aigu sévère (anatomopathologie)</term>
<term>Syndrome respiratoire aigu sévère (immunologie)</term>
<term>Syndrome respiratoire aigu sévère (virologie)</term>
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<term>Transduction du signal</term>
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<term>Virus du SRAS (pathogénicité)</term>
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<keywords scheme="MESH" qualifier="biosynthèse" xml:lang="fr"><term>ARN non traduit</term>
</keywords>
<keywords scheme="MESH" qualifier="immunologie" xml:lang="fr"><term>Syndrome respiratoire aigu sévère</term>
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="immunology" xml:lang="en"><term>SARS Virus</term>
<term>Severe Acute Respiratory Syndrome</term>
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<keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr"><term>Virus du SRAS</term>
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<keywords scheme="MESH" qualifier="pathology" xml:lang="en"><term>Severe Acute Respiratory Syndrome</term>
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<keywords scheme="MESH" qualifier="virologie" xml:lang="fr"><term>Syndrome respiratoire aigu sévère</term>
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<term>Disease Models, Animal</term>
<term>Gene Expression Profiling</term>
<term>Gene Expression Regulation</term>
<term>Immunity, Innate</term>
<term>Mice</term>
<term>Signal Transduction</term>
<term>Transcription, Genetic</term>
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<term>Immunité innée</term>
<term>Modèles animaux de maladie humaine</term>
<term>Régulation de l'expression des gènes</term>
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<front><div type="abstract" xml:lang="en">Studies of the host response to virus infection typically focus on protein-coding genes. However, non-protein-coding RNAs (ncRNAs) are transcribed in mammalian cells, and the roles of many of these ncRNAs remain enigmas. Using next-generation sequencing, we performed a whole-transcriptome analysis of the host response to severe acute respiratory syndrome coronavirus (SARS-CoV) infection across four founder mouse strains of the Collaborative Cross. We observed differential expression of approximately 500 annotated, long ncRNAs and 1,000 nonannotated genomic regions during infection. Moreover, studies of a subset of these ncRNAs and genomic regions showed the following. (i) Most were similarly regulated in response to influenza virus infection. (ii) They had distinctive kinetic expression profiles in type I interferon receptor and STAT1 knockout mice during SARS-CoV infection, including unique signatures of ncRNA expression associated with lethal infection. (iii) Over 40% were similarly regulated in vitro in response to both influenza virus infection and interferon treatment. These findings represent the first discovery of the widespread differential expression of long ncRNAs in response to virus infection and suggest that ncRNAs are involved in regulating the host response, including innate immunity. At the same time, virus infection models provide a unique platform for studying the biology and regulation of ncRNAs.</div>
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