Molecular mechanism of hTid-1, the human homolog of Drosophila tumor suppressor l(2)Tid, in the regulation of NF-kappaB activity and suppression of tumor growth

Mol Cell Biol. 2005 Jan;25(1):44-59. doi: 10.1128/MCB.25.1.44-59.2005.


hTid-1, a human homolog of the Drosophila tumor suppressor l(2)Tid and a novel DnaJ protein, regulates the activity of nuclear factor kappaB (NF-kappaB), but its mechanism is not established. We report here that hTid-1 strongly associated with the cytoplasmic protein complex of NF-kappaB-IkappaB through direct interaction with IkappaBalpha/beta and the IKKalpha/beta subunits of the IkappaB kinase complex. These interactions resulted in suppression of the IKK activity in a J-domain-dependent fashion and led to the cytoplasmic retention and enhanced stability of IkappaB. Overexpression of hTid-1 by using recombinant baculovirus or adenovirus led to inhibition of cell proliferation and induction of apoptosis of human osteosarcoma cells regardless of the p53 expression status. Adherent cultured cells transduced with Ad.hTid-1 detached from the dish surface. Morphological changes consistent with apoptosis and cell death were evident 48 h after Ad.EGFP-hTid-1 transduction. In contrast, cells transduced with Ad.EGFP or Ad.EGFP-hTd-1DeltaN100, a mutant that has the N-terminal J domain deletion and that lost suppressive activity on IKK, continued to proliferate. Similar data were obtained with A375 human melanoma cells. Ad.EGFP or Ad.EGFP-hTd-1DeltaN100 ex vivo-transduced A375 cells injected subcutaneously into nude mice produced growing tumors, whereas Ad.EGFP-hTid-1-transduced cells did not. Collectively, the data suggest that hTid-1 represses the activity of NF-kappaB through physical and functional interactions with the IKK complex and IkappaB and, in doing so, it modulates cell growth and death.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenoviridae / genetics
  • Adenoviridae / metabolism
  • Agar / metabolism
  • Animals
  • Apoptosis
  • Baculoviridae / metabolism
  • Cell Death
  • Cell Line
  • Cell Line, Tumor
  • Cell Proliferation
  • Cytoplasm / metabolism
  • Drosophila
  • Gene Deletion
  • Gene Expression Regulation
  • Genes, Reporter
  • Glutathione Transferase / metabolism
  • Green Fluorescent Proteins / metabolism
  • HSP40 Heat-Shock Proteins
  • Heat-Shock Proteins / chemistry
  • Heat-Shock Proteins / physiology*
  • Humans
  • I-kappa B Proteins / metabolism
  • Immunoprecipitation
  • Lentivirus / genetics
  • Male
  • Mice
  • Mice, Nude
  • Microscopy, Fluorescence
  • Mutation
  • NF-kappa B / metabolism*
  • Neoplasm Transplantation
  • Osteosarcoma / metabolism
  • Plasmids / metabolism
  • Protein Binding
  • Protein Structure, Tertiary
  • Recombinant Fusion Proteins / metabolism
  • Signal Transduction
  • Tetrazolium Salts / pharmacology
  • Thiazoles / pharmacology
  • Time Factors
  • Transfection
  • Tumor Suppressor Protein p53 / metabolism


  • DNAJA3 protein, human
  • HSP40 Heat-Shock Proteins
  • Heat-Shock Proteins
  • I-kappa B Proteins
  • NF-kappa B
  • Recombinant Fusion Proteins
  • Tetrazolium Salts
  • Thiazoles
  • Tumor Suppressor Protein p53
  • Green Fluorescent Proteins
  • Agar
  • Glutathione Transferase
  • thiazolyl blue