Fbw7 dimerization determines the specificity and robustness of substrate degradation

Genes Dev. 2013 Dec 1;27(23):2531-6. doi: 10.1101/gad.229195.113.

Abstract

The Fbw7 tumor suppressor targets a broad network of proteins for ubiquitylation. Here we show critical functions for Fbw7 dimerization in regulating the specificity and robustness of degradation. Dimerization enables Fbw7 to target substrates through concerted binding to two suboptimal and independent recognition sites. Accordingly, an endogenous dimerization-deficient Fbw7 mutation stabilizes suboptimal substrates. Dimerization increases Fbw7's robustness by preserving its function in the setting of mutations that disable Fbw7 monomers, thereby buffering against pathogenic mutations. Finally, dimerization regulates Fbw7 stability, and this likely involves Fbw7 trans-autoubiquitylation. Our study reveals novel functions of Fbw7 dimerization and an unanticipated complexity in substrate degradation.

Keywords: Fbw7; SCF; cyclin E; phosphodegron.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Motifs
  • Cell Cycle Proteins / chemistry
  • Cell Cycle Proteins / metabolism*
  • Dimerization
  • F-Box Proteins / chemistry
  • F-Box Proteins / metabolism*
  • F-Box-WD Repeat-Containing Protein 7
  • HCT116 Cells
  • Humans
  • Ligases / chemistry
  • Ligases / metabolism
  • Mutation
  • Protein Binding
  • Protein Stability
  • Substrate Specificity
  • Ubiquitin-Protein Ligases / chemistry
  • Ubiquitin-Protein Ligases / metabolism*
  • Ubiquitination

Substances

  • Cell Cycle Proteins
  • F-Box Proteins
  • F-Box-WD Repeat-Containing Protein 7
  • FBXW7 protein, human
  • Ubiquitin-Protein Ligases
  • Ligases