The binding of apobec-1 to mammalian apo B RNA is stabilized by the presence of complementation factors which are required for post-transcriptional editing

Nucleic Acids Symp Ser. 1995:(33):99-102.

Abstract

C to U RNA editing in mammalian intestinal apolipoprotein B mRNA creates an in-frame translational stop and the synthesis of a truncated protein called apo B48. This site specific cytidine deamination is mediated by an enzyme complex of which the catalytic component (apobec-1) is a 27 kDa zinc-binding protein. apobec-1, expressed in bacteria, will bind to mammalian apo B RNA as well as a number of other AU-rich RNA templates. Apo B RNA-binding activity can be competed by the addition of tRNA, an effect which can be overcome by the addition of complementation factors such as chick enterocyte S-100 extracts. Thus, apobec-1 may be a non-specific RNA binding protein which requires the presence of complementation factors to stabilize and enhance its binding in the setting of the holo-enzyme.

Publication types

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

MeSH terms

  • APOBEC-1 Deaminase
  • Animals
  • Apolipoproteins B / genetics*
  • Chickens
  • Cross-Linking Reagents
  • Cytidine Deaminase / metabolism*
  • Enzyme Stability
  • Glutathione Transferase / metabolism
  • In Vitro Techniques
  • Intestinal Mucosa / metabolism
  • RNA / genetics*
  • RNA / metabolism*
  • RNA Editing*
  • RNA Processing, Post-Transcriptional
  • RNA, Transfer / metabolism
  • Recombinant Fusion Proteins / metabolism
  • Ultraviolet Rays

Substances

  • Apolipoproteins B
  • Cross-Linking Reagents
  • Recombinant Fusion Proteins
  • RNA
  • RNA, Transfer
  • Glutathione Transferase
  • AICDA (activation-induced cytidine deaminase)
  • APOBEC-1 Deaminase
  • Cytidine Deaminase