Mutagenesis of apobec-1 complementation factor reveals distinct domains that modulate RNA binding, protein-protein interaction with apobec-1, and complementation of C to U RNA-editing activity

J Biol Chem. 2001 Dec 7;276(49):46386-93. doi: 10.1074/jbc.M107654200. Epub 2001 Sep 24.

Abstract

C to U editing of apolipoprotein B (apoB) RNA requires a multicomponent holoenzyme complex in which minimal constituents include apobec-1 and apobec-1 complementation factor (ACF). We have examined the predicted functional domains in ACF in binding apoB RNA, interaction with apobec-1, and complementation of RNA editing. We demonstrate that apoB RNA binding and apobec-1-interacting domains are defined by two partially overlapping regions containing the NH(2)-terminal RNA recognition motifs of ACF. Both apoB RNA binding and apobec-1 interaction are required for editing complementation activity. ACF is a nuclear protein that upon cotransfection with apobec-1 results in nuclear colocalization and redistribution of apobec-1 from the cytoplasm. ACF constructs with deletions or mutations in the putative nuclear localization signal (NLS) still localize in the nucleus of transfected cells but do not colocalize with apobec-1, the latter remaining predominantly cytoplasmic. These observations suggest that the putative NLS motif in ACF is not responsible for its nucleo-cytoplasmic trafficking. By contrast, protein-protein interaction is important for the nuclear import of apobec-1. Taken together, these data suggest that functional complementation of C to U RNA editing by apobec-1 involves the NH(2)-terminal 380 residues of ACF.

Publication types

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

MeSH terms

  • APOBEC-1 Deaminase
  • Animals
  • Apolipoproteins B / metabolism
  • Base Sequence
  • Cell Line
  • Cloning, Molecular
  • Cytidine Deaminase*
  • DNA Primers
  • Mutagenesis
  • RNA / metabolism*
  • RNA Editing*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • RNA-Binding Proteins / physiology*
  • Rats
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Sequence Deletion

Substances

  • Apolipoproteins B
  • DNA Primers
  • RNA-Binding Proteins
  • Recombinant Proteins
  • RNA
  • APOBEC-1 Deaminase
  • Apobec1 protein, rat
  • Cytidine Deaminase