The HIV-1 Nef protein enhances the affinity of reverse transcriptase for RNA in vitro

Virus Genes. 2002 Dec;25(3):255-69. doi: 10.1023/a:1020971823562.

Abstract

Several viral proteins, including nucleocapsid protein, integrase, Vif, Tat, and Nef have been proposed to act as cofactors of HIV-1 reverse transcription. Using two viral RNA probes, one overlapping the primer-binding site (PBS) and the other representing the ribosomal frameshifting signal (FS) of HIV-1 RNA, we found that recombinant full-length Nef protein (NefLAI) increased the affinity of reverse transcriptase (RT) for RNA in vitro, and interacted directly with RT in protein co-precipitation assays. The effect on RT-RNA binding and the capacity of Nef to interact with RT was also observed with N-terminal deletion mutant NefDelta57 and NefSF2, although to a lesser level. NefDelta57 corresponded to the processed Nef protein present in the internal core of mature virions, and lacked the N-myristoylated N-terminus and N-terminal region implicated in virus infectivity and pathogenicity in vivo. NefSF2, a Nef allele from a highly pathogenic strain of HIV-1, differed from NefLAI by the amino acid sequence and immunoreactivity of its N-terminal domain. The effect observed with NefSF2 and NefDelta57, and data from phage biopanning experiments suggested that the RT-binding region in Nef involved the C-terminal flexible loop of its C-terminal domain, but the function in RT-RNA binding was also influenced by its N-terminal domain.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Binding Sites
  • Electrophoretic Mobility Shift Assay
  • Gene Products, nef / metabolism*
  • HIV-1 / genetics*
  • HIV-1 / metabolism
  • Humans
  • In Vitro Techniques
  • Molecular Sequence Data
  • Protein Footprinting
  • RNA / genetics
  • RNA / metabolism*
  • RNA-Directed DNA Polymerase / metabolism*
  • nef Gene Products, Human Immunodeficiency Virus

Substances

  • Gene Products, nef
  • nef Gene Products, Human Immunodeficiency Virus
  • RNA
  • RNA-Directed DNA Polymerase