Effect of HIV integrase inhibitors on the RAG1/2 recombinase

Proc Natl Acad Sci U S A. 2002 Jan 8;99(1):134-7. doi: 10.1073/pnas.012610699. Epub 2001 Dec 26.

Abstract

Assembly of functional Ig and T cell receptor genes by V(D)J recombination depends on site-specific cleavage of chromosomal DNA by the RAG1/2 recombinase. As RAG1/2 action has mechanistic similarities to DNA transposases and integrases such as HIV-1 integrase, we sought to determine how integrase inhibitors of the diketo acid type would affect the various activities of RAG1/2. Both of the inhibitors we tested interfered with DNA cleavage and disintegration activities of RAG1/2, apparently by disrupting interaction with the DNA motifs bound specifically by the recombinase. The inhibitors did not ablate RAG1/2's transposition activity or capture of nonspecific transpositional target DNA, suggesting this DNA occupies a site on the recombinase different from that used for specific binding. These results further underscore the similarities between RAG1/2 and integrase and suggest that certain integrase inhibitors may have the potential to interfere with aspects of B and T cell development.

MeSH terms

  • Amino Acid Motifs
  • Animals
  • Calcium / pharmacology
  • Cell-Free System
  • DNA-Binding Proteins / metabolism*
  • Dose-Response Relationship, Drug
  • Electrophoresis, Polyacrylamide Gel
  • Enzyme Inhibitors / pharmacology*
  • HIV Integrase Inhibitors / pharmacology*
  • Homeodomain Proteins / metabolism*
  • Magnesium / pharmacology
  • Mice
  • Models, Biological
  • Protein Binding
  • Recombination, Genetic*
  • Time Factors

Substances

  • DNA-Binding Proteins
  • Enzyme Inhibitors
  • HIV Integrase Inhibitors
  • Homeodomain Proteins
  • Rag2 protein, mouse
  • V(D)J recombination activating protein 2
  • RAG-1 protein
  • Magnesium
  • Calcium