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Enhanced SUMOylation in polyglutamine diseases

Authors :
Xia Lin
Hideji Hashida
Ichiro Kanazawa
Jun Goto
Kiyomitsu Oyanagi
Hiroko Ueda
Huda Y. Zoghbi
Hitoshi Kawano
Hitoshi Okazawa
Source :
Biochemical and Biophysical Research Communications. 293:307-313
Publication Year :
2002
Publisher :
Elsevier BV, 2002.

Abstract

Small ubiquitin-like modifiers (SUMOs) are proteins homologous to ubiquitin that possibly regulate intranuclear protein localization, nuclear transport, and ubiquitination. We examined patients of DRPLA, SCA1, MJD, and Huntington's disease and found that neurons in affected regions of the brain react strongly to SUMO-1, a family member of SUMOs. Western blot with a transgenic mouse expressing mutant ataxin-1 showed the increase of SUMOylated proteins in the cerebellar cortex, which we named ESCA1 and ESCA2. These results indicated activation of SUMO-1 system in polyglutamine diseases and predicted its involvement in the pathology.

Details

ISSN :
0006291X
Volume :
293
Database :
OpenAIRE
Journal :
Biochemical and Biophysical Research Communications
Accession number :
edsair.doi.dedup.....c4234eafbd67ae86ba00145045105da3
Full Text :
https://doi.org/10.1016/s0006-291x(02)00211-5