Huntingtin is ubiquitinated and interacts with a specific ubiquitin-conjugating enzyme

  • J Biol Chem. 1996 Aug 9;271(32):19385-94. doi: 10.1074/jbc.271.32.19385.
M A Kalchman  1 R K Graham G Xia H B Koide J G Hodgson K C Graham Y P Goldberg R D Gietz C M Pickart M R Hayden
Affiliations
  • 1. Department of Medical Genetics, University of British Columbia, Vancouver, British Columbia, Canada V6T 1Z4.
Abstract

Using the yeast two-hybrid system, we have identified a human ubiquitin-conjugating enzyme (hE2-25K) as a protein that interacts with the gene product for Huntington disease (HD) (Huntingtin). This protein has complete amino acid identity with the bovine E2-25K protein and has striking similarity to the UBC-1, -4 and -5 Enzymes of Saccharomyces cerevisiae. This protein is highly expressed in brain and a slightly larger protein recognized by an anti-E2-25K polyclonal antibody is selectively expressed in brain regions affected in HD. The huntingtin-E2-25K interaction is not obviously modulated by CAG length. We also demonstrate that Huntingtin is ubiquitinated. These findings have implications for the regulated catabolism of the gene product for HD.