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A novel ubiquitin‐binding protein ZNF216 functioning in muscle atrophy
Author(s) -
Hishiya Akinori,
Iemura Shunichiro,
Natsume Tohru,
Takayama Shinichi,
Ikeda Kyoji,
Watanabe Ken
Publication year - 2006
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/sj.emboj.7600945
Subject(s) - library science , geriatrics , gerontology , medicine , family medicine , computer science , psychiatry
The ubiquitin–proteasome system (UPS) is critical for specific degradation of cellular proteins and plays a pivotal role on protein breakdown in muscle atrophy. Here, we show that ZNF216 directly binds polyubiquitin chains through its N‐terminal A20‐type zinc‐finger domain and associates with the 26S proteasome. ZNF216 was colocalized with the aggresome, which contains ubiquitinylated proteins and other UPS components. Expression of Znf216 was increased in both denervation‐ and fasting‐induced muscle atrophy and upregulated by expression of constitutively active FOXO, a master regulator of muscle atrophy. Mice deficient in Znf216 exhibited resistance to denervation‐induced atrophy, and ubiquitinylated proteins markedly accumulated in neurectomized muscle compared to wild‐type mice. These data suggest that ZNF216 functions in protein degradation via the UPS and plays a crucial role in muscle atrophy.