| Literature DB >> 25343992 |
Peng Yin1, Zhuchi Tu1, An Yin1, Ting Zhao2, Sen Yan3, Xiangyu Guo1, Renbao Chang1, Lianhe Zhang1, Yan Hong2, Xiahe Huang1, Junxia Zhou1, Yingchun Wang1, Shihua Li2, Xiao-Jiang Li4.
Abstract
Although misfolded proteins are ubiquitinated and cleared by the proteasome, they can accumulate in synapses in aged neurons to promote synaptic dysfunction in a variety of neurodegenerative diseases, including Huntington's disease (HD), which is caused by polyglutamine expansion in huntingtin. The mechanism behind this aging-related phenomenon is unknown and has been difficult to investigate using animals with short life spans. With brain tissues from longer-lived rhesus monkeys of different ages, we found that aging reduces ubiquitin-proteasomal activity and also increases the level of ubiquitin-conjugating enzyme UBE2N (Ubc13) in synaptosomes. Synaptosomal fractions from aged monkey brain increase in vitro ubiquitinated huntingtin, whereas depletion of UBE2N markedly reduces this increase. Overexpressing UBE2N increases the aggregation of mutant huntingtin, and reducing UBE2N attenuates huntingtin aggregation in cellular and mouse models of HD. Our studies suggest that increased UBE2N plays a critical role in the synaptosomal accumulation of mutant huntingtin with age.Entities:
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Year: 2014 PMID: 25343992 PMCID: PMC4321442 DOI: 10.1093/hmg/ddu544
Source DB: PubMed Journal: Hum Mol Genet ISSN: 0964-6906 Impact factor: 6.150