Dynamic evolution of the human immunodeficiency virus type 1 pathogenic factor, Nef

J Virol. 2006 Feb;80(3):1311-20. doi: 10.1128/JVI.80.3.1311-1320.2006.

Abstract

The human immunodeficiency virus type 1 (HIV-1) early gene product Nef is a multifunctional protein that alters numerous pathways of T-cell function, including endocytosis, signal transduction, vesicular trafficking, and immune modulation, and is a major determinant of pathogenesis. Individual Nef functions include PAK-2 activation, CD4 downregulation, major histocompatibility complex (MHC) class I downregulation, and enhancement of viral particle infectivity. How Nef accomplishes its multiple tasks presents a difficult problem of mechanistic analysis because of the complications associated with multiple, overlapping functional domains in the context of significant sequence variability. To address these issues we determined the conservation of each Nef residue based on 1,643 subtype B Nef sequences. Mutational analysis based on conservative substitutions and Nef sequence data allowed us to search for amino acids on the surface of Nef that are specifically required for PAK-2 activation. We found residues 85, 89, and 191 to be highly significant determinants for Nef's PAK-2 activation function but functionally unlinked to CD4 and MHC class I downregulation or enhancement of infectivity. These residues are not conserved across HIV-1 subtypes but are confined to separate sets of surface elements within a subtype. Thus, L85/H89/F191 and F85/F89/R191 are dominant in subtype B and subtype E or C, respectively. Our results provide support for developing subtype-specific interventions in HIV-1 disease.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Amino Acid Sequence
  • Amino Acid Substitution
  • Cell Line
  • Conserved Sequence
  • Databases, Protein
  • Enzyme Activation
  • Evolution, Molecular*
  • Gene Products, nef / chemistry
  • Gene Products, nef / genetics*
  • Gene Products, nef / physiology
  • HIV-1 / classification
  • HIV-1 / genetics*
  • HIV-1 / pathogenicity
  • HIV-1 / physiology
  • HeLa Cells
  • Humans
  • In Vitro Techniques
  • Mutagenesis, Site-Directed
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Structure, Tertiary
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Virulence / genetics
  • Virulence / physiology
  • nef Gene Products, Human Immunodeficiency Virus
  • p21-Activated Kinases

Substances

  • Gene Products, nef
  • Recombinant Proteins
  • nef Gene Products, Human Immunodeficiency Virus
  • PAK2 protein, human
  • Protein Serine-Threonine Kinases
  • p21-Activated Kinases