Hyperediting of human T-cell leukemia virus type 2 and simian T-cell leukemia virus type 3 by the dsRNA adenosine deaminase ADAR-1
Autor: | Nga Ling Ko, Jean-Pierre Vartanian, Renaud Mahieux, Emmanuel Birlouez, Simon Wain-Hobson |
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Přispěvatelé: | Epidémiologie et Physiopathologie des Virus Oncogènes, Institut Pasteur [Paris] (IP)-Centre National de la Recherche Scientifique (CNRS), Rétrovirologie Moléculaire, Institut Pasteur [Paris] (IP), Oncogenèse rétrovirale – Retroviral Oncogenesis (OR), Centre International de Recherche en Infectiologie - UMR (CIRI), École normale supérieure - Lyon (ENS Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure - Lyon (ENS Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), This work was supported by funds from the Institut Pasteur the CNRS and the DGA (Direction Générale des Armées). The Molecular Retrovirology Unit is ‘Equipe labellisée LIGUE 2010’. R. M. is supported by Ecole Normale Supérieure de Lyon, by INSERM and through funding from the Programme interdisciplinaire CNRS Maladies infectieuses émergentes and from NIH (grant AI072495-01)., Vartanian, Jean-Pierre, Centre International de Recherche en Infectiologie (CIRI), École normale supérieure de Lyon (ENS de Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS)-École normale supérieure de Lyon (ENS de Lyon)-Université Claude Bernard Lyon 1 (UCBL), Université de Lyon-Université de Lyon-Université Jean Monnet - Saint-Étienne (UJM)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS) |
Jazyk: | angličtina |
Rok vydání: | 2012 |
Předmět: |
MESH: Simian T-lymphotropic virus 3
Adenosine MESH: Mutation Adenosine Deaminase viruses [SDV]Life Sciences [q-bio] Molecular Sequence Data T-cell leukemia Viral transformation Genome Viral MESH: Base Sequence Polymerase Chain Reaction MESH: Sequence Homology Nucleic Acid Virus Adenosine deaminase Sequence Homology Nucleic Acid Virology Animals Humans MESH: RNA Editing MESH: Animals MESH: Adenosine Deaminase Simian T-lymphotropic virus 3 MESH: Humans MESH: Molecular Sequence Data Base Sequence biology MESH: Human T-lymphotropic virus 2 Animal Human T-lymphotropic virus 2 RNA-Binding Proteins RNA MESH: Polymerase Chain Reaction MESH: Adenosine Molecular biology [SDV] Life Sciences [q-bio] HEK293 Cells MESH: RNA-Binding Proteins RNA editing MESH: HEK293 Cells MESH: RNA Viral Mutation ADAR biology.protein RNA Viral RNA Editing MESH: Genome Viral |
Zdroj: | Journal of General Virology Journal of General Virology, 2012, 93 (12), pp.2646-2651. ⟨10.1099/vir.0.045146-0⟩ |
ISSN: | 0022-1317 1465-2099 |
DOI: | 10.1099/vir.0.045146-0⟩ |
Popis: | RNA editing mediated by adenosine deaminases acting on RNA (ADARs) converts adenosine (A) to inosine (I) residues in dsRNA templates. While ADAR-1-mediated editing was essentially described for RNA viruses, the present work addresses the issue for two δ-retroviruses, human T-cell leukemia virus type 2 and simian T-cell leukemia virus type 3 (HTLV-2 and STLV-3). We examined whether ADAR-1 could edit HTLV-2 and STLV-3 virus genomes in cell culture andin vivo. Using a highly sensitive PCR-based method, referred to as 3DI-PCR, we showed that ADAR-1 could hypermutate adenosine residues in HTLV-2. STLV-3 hypermutation was obtained without using 3DI-PCR, suggesting a higher mutation frequency for this virus. Detailed analysis of the dinucleotide editing context showed preferences for 5′ ArA and 5′ UrA. In conclusion, the present observations demonstrate that ADAR-1 massively edits HTLV-2 and STLV-3 retrovirusesin vitro, but probably remains a rare phenomenonin vivo. |
Databáze: | OpenAIRE |
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