Initiation of HIV-1 reverse transcription and functional role of nucleocapsid-mediated tRNA/viral genome interactions

Virus Res. 2012 Nov;169(2):324-39. doi: 10.1016/j.virusres.2012.06.006. Epub 2012 Jun 18.

Abstract

HIV-1 reverse transcription is initiated from a tRNA(Lys)(3) molecule annealed to the viral RNA at the primer binding site (PBS). The annealing of tRNA(Lys)(3) requires the opening of its three-dimensional structure and RNA rearrangements to form an efficient initiation complex recognized by the reverse transcriptase. This annealing is mediated by the nucleocapsid protein (NC). In this paper, we first review the actual knowledge about HIV-1 viral RNA and tRNA(Lys)(3) structures. Then, we summarize the studies explaining how NC chaperones the formation of the tRNA(Lys)(3)/PBS binary complex. Additional NMR data that investigated the NC interaction with tRNA(Lys)(3) D-loop are presented. Lastly, we focused on the additional interactions occurring between tRNA(Lys)(3) and the viral RNA and showed that they are dependent on HIV-1 isolates, i.e. the sequence and the structure of the viral RNA.

Publication types

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

MeSH terms

  • HIV-1 / physiology*
  • Magnetic Resonance Spectroscopy
  • Molecular Chaperones / metabolism
  • Nucleic Acid Conformation
  • RNA, Transfer, Lys / chemistry
  • RNA, Transfer, Lys / metabolism*
  • RNA, Viral / chemistry
  • RNA, Viral / metabolism*
  • Reverse Transcription*
  • gag Gene Products, Human Immunodeficiency Virus / chemistry
  • gag Gene Products, Human Immunodeficiency Virus / metabolism

Substances

  • Molecular Chaperones
  • NCP7 protein, Human immunodeficiency virus 1
  • RNA, Transfer, Lys
  • RNA, Viral
  • gag Gene Products, Human Immunodeficiency Virus