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WeightNameValue
1000 Titel
  • RESIC: A Tool for Comprehensive Adenosine to Inosine RNA Editing Site Identification and Classification
1000 Autor/in
  1. Light, Dean |
  2. Haas, Roni |
  3. Yazbak, Mahmoud |
  4. Elfand, Tal |
  5. Blau, Tal |
  6. Lamm, Ayelet T. |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-07-23
1000 Erschienen in
1000 Quellenangabe
  • 12:686851
1000 Copyrightjahr
  • 2021
1000 Embargo
  • 2022-01-25
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.3389/fgene.2021.686851 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8343188/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Abstract/Summary
  • <jats:p>Adenosine to inosine (A-to-I) RNA editing, the most prevalent type of RNA editing in metazoans, is carried out by adenosine deaminases (ADARs) in double-stranded RNA regions. Several computational approaches have been recently developed to identify A-to-I RNA editing sites from sequencing data, each addressing a particular issue. Here, we present RNA Editing Sites Identification and Classification (RESIC), an efficient pipeline that combines several approaches for the detection and classification of RNA editing sites. The pipeline can be used for all organisms and can use any number of RNA-sequencing datasets as input. RESIC provides (1) the detection of editing sites in both repetitive and non-repetitive genomic regions; (2) the identification of hyper-edited regions; and (3) optional exclusion of polymorphism sites to increase reliability, based on DNA, and ADAR-mutant RNA sequencing datasets, or SNP databases. We demonstrate the utility of RESIC by applying it to human, successfully overlapping and extending the list of known putative editing sites. We further tested changes in the patterns of A-to-I RNA editing, and RNA abundance of ADAR enzymes, following SARS-CoV-2 infection in human cell lines. Our results suggest that upon SARS-CoV-2 infection, compared to mock, the number of hyper editing sites is increased, and in agreement, the activity of ADAR1, which catalyzes hyper-editing, is enhanced. These results imply the involvement of A-to-I RNA editing in conceiving the unpredicted phenotype of COVID-19 disease. RESIC code is open-source and is easily extendable.</jats:p>
1000 Sacherschließung
lokal epitranscriptome
lokal ADAR
lokal Genetics
lokal hyper-editing
lokal interferon
lokal SARS-CoV-2
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/TGlnaHQsIERlYW4=|https://frl.publisso.de/adhoc/uri/SGFhcywgUm9uaQ==|https://frl.publisso.de/adhoc/uri/WWF6YmFrLCBNYWhtb3Vk|https://frl.publisso.de/adhoc/uri/RWxmYW5kLCBUYWw=|https://frl.publisso.de/adhoc/uri/QmxhdSwgVGFs|https://frl.publisso.de/adhoc/uri/TGFtbSwgQXllbGV0IFQu
1000 Hinweis
  • DeepGreen-ID: 4abcca50889e45b5857983a49df74f5c ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
1000 Label
1000 Förderer
  1. Division of Molecular and Cellular Biosciences |
1000 Fördernummer
  1. -
1000 Förderprogramm
  1. -
1000 Dateien
1000 Förderung
  1. 1000 joinedFunding-child
    1000 Förderer Division of Molecular and Cellular Biosciences |
    1000 Förderprogramm -
    1000 Fördernummer -
1000 Objektart article
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1000 @id frl:6476775.rdf
1000 Erstellt am 2024-05-14T14:31:12.869+0200
1000 Erstellt von 322
1000 beschreibt frl:6476775
1000 Zuletzt bearbeitet 2024-05-15T08:27:25.164+0200
1000 Objekt bearb. Wed May 15 08:27:25 CEST 2024
1000 Vgl. frl:6476775
1000 Oai Id
  1. oai:frl.publisso.de:frl:6476775 |
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