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Elife ; 5: e11275, 2016 Mar 24.
Article in English | MEDLINE | ID: mdl-27011352

ABSTRACT

The RIG-I-like receptors (RLRs) play a major role in sensing RNA virus infection to initiate and modulate antiviral immunity. They interact with particular viral RNAs, most of them being still unknown. To decipher the viral RNA signature on RLRs during viral infection, we tagged RLRs (RIG-I, MDA5, LGP2) and applied tagged protein affinity purification followed by next-generation sequencing (NGS) of associated RNA molecules. Two viruses with negative- and positive-sense RNA genome were used: measles (MV) and chikungunya (CHIKV). NGS analysis revealed that distinct regions of MV genome were specifically recognized by distinct RLRs: RIG-I recognized defective interfering genomes, whereas MDA5 and LGP2 specifically bound MV nucleoprotein-coding region. During CHIKV infection, RIG-I associated specifically to the 3' untranslated region of viral genome. This study provides the first comparative view of the viral RNA ligands for RIG-I, MDA5 and LGP2 in the presence of infection.


Subject(s)
Chikungunya virus/immunology , DEAD Box Protein 58/metabolism , Interferon-Induced Helicase, IFIH1/metabolism , Measles virus/immunology , RNA Helicases/metabolism , RNA, Viral/metabolism , Receptors, Immunologic/metabolism , Cell Line , High-Throughput Nucleotide Sequencing , Humans , Interferon-Induced Helicase, IFIH1/isolation & purification , RNA Helicases/isolation & purification , RNA, Viral/genetics , Receptors, Immunologic/isolation & purification
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