Single-strand specificity of APOBEC3G accounts for minus-strand deamination of the HIV genome

Nat Struct Mol Biol. 2004 May;11(5):435-42. doi: 10.1038/nsmb758. Epub 2004 Apr 18.

Abstract

HIV-1 deleted for the vif accessory gene encapsidates the cellular cytidine deaminase APOBEC3G. Upon infection, the encapsidated APOBEC3G induces G-->A mutations in the viral reverse transcripts. The G-->A mutations result either from C-->U deamination of the minus strand or deamination of both strands followed by repair of the plus strand. We report here that minus-strand deamination occurred over the length of the virus genome, preferentially at CCCA sequences, with a graded frequency in the 5'-->3' direction. APOBEC3G induced previously undetected C-->T mutations in the 5' U3 and the primer-binding site, both of which become transiently single-stranded during reverse transcription. In vitro, APOBEC3G bound and deaminated single-stranded DNA (ssDNA) but not double-stranded DNA (dsDNA) or DNA-RNA hybrids. We propose that the requirement for ssDNA accounts for the minus-strand mutations, the 5'-->3' graded frequency of deamination and the rare C-->T mutations.

Publication types

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

MeSH terms

  • APOBEC-3G Deaminase
  • Cytidine Deaminase
  • Genome, Viral*
  • HIV / genetics*
  • Nucleoside Deaminases
  • Proteins / metabolism*
  • Proteins / physiology
  • RNA, Messenger / genetics
  • Recombinant Proteins / metabolism
  • Repressor Proteins

Substances

  • Proteins
  • RNA, Messenger
  • Recombinant Proteins
  • Repressor Proteins
  • Nucleoside Deaminases
  • APOBEC-3G Deaminase
  • APOBEC3G protein, human
  • Cytidine Deaminase