Correlation Engine 2.0
Clear Search sequence regions


  • ADAR1 (1)
  • ADAR2 (1)
  • ADAR3 (1)
  • alu elements (1)
  • base pairs (1)
  • cellular (2)
  • d rna (1)
  • genes (1)
  • interferon (1)
  • mammals (1)
  • microrna (1)
  • mrna (1)
  • p110 (1)
  • polyomavirus (1)
  • receptor (1)
  • responses interferon (1)
  • rna (14)
  • rna viral (1)
  • rna viral (1)
  • Sizes of these terms reflect their relevance to your search.

    C6 deamination of adenosine (A) to inosine (I) in double-stranded RNA (dsRNA) is catalyzed by a family of enzymes known as ADARs (adenosine deaminases acting on RNA) encoded by three genes in mammals. Alternative promoters and splicing produce two ADAR1 proteins, an interferon-inducible cytoplasmic p150 and a constitutively expressed p110 that like ADAR2 is a nuclear enzyme. ADAR3 lacks deaminase activity. A-to-I editing occurs with both viral and cellular RNAs. Deamination activity is dependent on dsRNA substrate structure and regulatory RNA-binding proteins and ranges from highly site selective with hepatitis D RNA and glutamate receptor precursor messenger RNA (pre-mRNA) to hyperediting of measles virus and polyomavirus transcripts and cellular inverted Alu elements. Because I base-pairs as guanosine instead of A, editing can alter mRNA decoding, pre-mRNA splicing, and microRNA silencing. Editing also alters dsRNA structure, thereby suppressing innate immune responses including interferon production and action.

    Citation

    Christian K Pfaller, Cyril X George, Charles E Samuel. Adenosine Deaminases Acting on RNA (ADARs) and Viral Infections. Annual review of virology. 2021 Sep 29;8(1):239-264

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 33882257

    View Full Text