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

被引:292
作者
Kalchman, MA
Graham, RK
Xia, G
Koide, HB
Hodgson, JG
Graham, KC
Goldberg, YP
Gietz, RD
Pickart, CM
Hayden, MR
机构
[1] UNIV BRITISH COLUMBIA,DEPT MED GENET,VANCOUVER,BC V6T 1Z4,CANADA
[2] JOHNS HOPKINS UNIV,SCH PUBL HLTH,DEPT BIOCHEM,BALTIMORE,MD 21205
[3] UNIV MANITOBA,DEPT HUMAN GENET,WINNIPEG,MB R3E 0W3,CANADA
关键词
D O I
10.1074/jbc.271.32.19385
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:19385 / 19394
页数:10
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