RNA editing and immune control: from mechanism to therapy

Curr Opin Genet Dev. 2024 Jun:86:102195. doi: 10.1016/j.gde.2024.102195. Epub 2024 Apr 20.

Abstract

Adenosine-to-inosine RNA editing, catalyzed by the enzymes ADAR1 and ADAR2, stands as a pervasive RNA modification. A primary function of ADAR1-mediated RNA editing lies in labeling endogenous double-stranded RNAs (dsRNAs) as 'self', thereby averting their potential to activate innate immune responses. Recent findings have highlighted additional roles of ADAR1, independent of RNA editing, that are crucial for immune control. Here, we focus on recent progress in understanding ADAR1's RNA editing-dependent and -independent roles in immune control. We describe how ADAR1 regulates various dsRNA innate immune receptors through distinct mechanisms. Furthermore, we discuss the implications of ADAR1 and RNA editing in diseases, including autoimmune diseases and cancers.

Publication types

  • Review

MeSH terms

  • Adenosine Deaminase / genetics
  • Adenosine Deaminase / metabolism
  • Animals
  • Autoimmune Diseases / genetics
  • Autoimmune Diseases / immunology
  • Humans
  • Immunity, Innate*
  • Neoplasms / genetics
  • Neoplasms / immunology
  • Neoplasms / therapy
  • RNA Editing*
  • RNA, Double-Stranded / genetics
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism

Substances

  • ADAR protein, human
  • Adenosine Deaminase
  • RNA, Double-Stranded
  • RNA-Binding Proteins