Double-stranded RNA-specific adenosine deaminase: nucleic acid binding properties

Methods. 1998 Jul;15(3):199-205. doi: 10.1006/meth.1998.0624.

Abstract

The RNA-specific adenosine deaminase (ADAR1, herein referred to as ADAR) is an interferon-inducible RNA-editing enzyme. ADAR catalyzes the C-6 deamination of adenosine in double-stranded (ds) structures present in viral RNAs and cellular pre-mRNAs as well as synthetic dsRNA substrates. ADAR possesses three functionally distinct copies of the highly conserved double-stranded RNA binding R motif (RI, RII, RIII) implicated in the recognition of dsRNA structures within the substrate RNAs. ADAR is also a Z-DNA-binding protein. Two Z-DNA binding motifs (Zalpha and Zbeta) present in ADAR correspond to repeated regions homologous to the N-terminal region of the vaccinia virus E3L protein. Here we describe assay methods for measurement of ADAR enzymatic activity, dsRNA binding activity, and Z-DNA binding activity.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenosine Deaminase / genetics
  • Adenosine Deaminase / metabolism*
  • Animals
  • COS Cells
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • Genetic Vectors
  • Protein Binding
  • RNA-Binding Proteins
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism

Substances

  • DNA-Binding Proteins
  • RNA-Binding Proteins
  • Recombinant Proteins
  • ADARB1 protein, human
  • Adenosine Deaminase