DOT1L/H3K79me2 represses HIV-1 reactivation via recruiting DCAF1

Cell Rep. 2024 Jul 23;43(7):114368. doi: 10.1016/j.celrep.2024.114368. Epub 2024 Jun 20.

Abstract

DOT1L mediates the methylation of histone H3 at lysine 79 and, in turn, the transcriptional activation or repression in a context-dependent manner, yet the regulatory mechanisms and functions of DOT1L/H3K79me remain to be fully explored. Following peptide affinity purification and proteomic analysis, we identified that DCAF1-a component of the E3 ligase complex involved in HIV regulation-is associated with H3K79me2 and DOT1L. Interestingly, blocking the expression or catalytic activity of DOT1L or repressing the expression of DCAF1 significantly enhances the tumor necrosis factor alpha (TNF-α)/nuclear factor κB (NF-κB)-induced reactivation of the latent HIV-1 genome. Mechanistically, upon TNF-α/NF-κB activation, DCAF1 is recruited to the HIV-1 long terminal repeat (LTR) by DOT1L and H3K79me2. Recruited DCAF1 subsequently induces the ubiquitination of NF-κB and restricts its accumulation at the HIV-1 LTR. Altogether, our findings reveal a feedback modulation of HIV reactivation by DOT1L-mediated histone modification regulation and highlight the potential of targeting the DOT1L/DCAF1 axis as a therapeutic strategy for HIV treatment.

Keywords: CP: Microbiology; CP: Molecular biology; DCAF1; DOT1L; H3K79me2; HIV-1 reactivation; NF-κB.

MeSH terms

  • HEK293 Cells
  • HIV Infections / metabolism
  • HIV Infections / virology
  • HIV Long Terminal Repeat / genetics
  • HIV-1* / metabolism
  • HIV-1* / physiology
  • Histone-Lysine N-Methyltransferase* / genetics
  • Histone-Lysine N-Methyltransferase* / metabolism
  • Histones* / metabolism
  • Humans
  • Lysine / metabolism
  • Methylation
  • NF-kappa B* / metabolism
  • Protein Serine-Threonine Kinases
  • Tumor Necrosis Factor-alpha / metabolism
  • Ubiquitin-Protein Ligases* / metabolism
  • Ubiquitination
  • Virus Activation

Substances

  • Histone-Lysine N-Methyltransferase
  • DOT1L protein, human
  • Histones
  • NF-kappa B
  • Ubiquitin-Protein Ligases
  • DCAF1 protein, human
  • Tumor Necrosis Factor-alpha
  • Lysine
  • Protein Serine-Threonine Kinases