Huntingtin Is Ubiquitinated and Interacts with a Specific Ubiquitin-conjugating Enzyme
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...
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Veröffentlicht in: | The Journal of biological chemistry 1996-08, Vol.271 (32), p.19385-19394 |
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Sprache: | eng |
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Zusammenfassung: | 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, â4 and â5 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. |
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ISSN: | 0021-9258 1083-351X |
DOI: | 10.1074/jbc.271.32.19385 |