Induction of homologue of Slimb ubiquitin ligase receptor by mitogen signaling

J Biol Chem. 2002 Sep 27;277(39):36624-30. doi: 10.1074/jbc.M204524200. Epub 2002 Jul 31.

Abstract

Homologue of Slimb (HOS) is the substrate-recognizing component of the SCF(HOS)-Roc1 E3 ubiquitin protein ligase. This ligase mediates ubiquitination of the inhibitor of NF-kappaB transcription factor (IkappaB). We have found that HOS is highly expressed in a number of human cancer cell lines. The rates of the HOS gene transcription as well as HOS mRNA and protein levels were up-regulated in cells treated with mitogens or transfected with the inducers of mitogen-activated protein kinase pathway. Conversely, mitogen withdrawal strikingly reduced HOS levels during differentiation of mouse myoblasts. Activators of mitogen-activated protein kinase accelerated IkappaBalpha degradation and increased NF-kappaB transcriptional activity. Inhibition of HOS function via expression of dominant negative HOS (HOS(DeltaF)) initiated mouse myoblast differentiation and prevented Ras-mediated acceleration of IkappaBalpha degradation as well as NF-kappaB trans-activation and transformation of NIH3T3 cells. These data link the induction of HOS in proliferating cells with mitogen-signaling-dependent inhibition of cell differentiation and promotion of cell transformation.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Animals
  • Blotting, Northern
  • Cell Differentiation
  • Cell Nucleus / metabolism
  • Cell Transformation, Neoplastic
  • Dose-Response Relationship, Drug
  • Down-Regulation
  • Enzyme Activation
  • Fibroblasts / metabolism
  • Genes, Dominant
  • Humans
  • Immunoblotting
  • Ligases / metabolism*
  • Mice
  • Mitogens / metabolism*
  • NF-kappa B / metabolism
  • Ornithine Decarboxylase / metabolism
  • Precipitin Tests
  • Signal Transduction
  • Time Factors
  • Tumor Cells, Cultured
  • Ubiquitin / metabolism*

Substances

  • Mitogens
  • NF-kappa B
  • Ubiquitin
  • Ornithine Decarboxylase
  • Ligases