| Literature DB >> 24297164 |
John Hanna1, David Waterman, Marta Isasa, Suzanne Elsasser, Yuan Shi, Steven Gygi, Daniel Finley.
Abstract
Protein misfolding is a universal threat to cells. The ubiquitin-proteasome system mediates a cellular stress response capable of eliminating misfolded proteins. Here we identify Cuz1/Ynl155w as a component of the ubiquitin system, capable of interacting with both the proteasome and Cdc48. Cuz1/Ynl155w is regulated by the transcription factor Rpn4, and is required for cells to survive exposure to the trivalent metalloids arsenic and antimony. A related protein, Yor052c, shows similar phenotypes, suggesting a multicomponent stress response pathway. Cuz1/Ynl155w functions as a zinc-dependent ubiquitin-binding protein. Thus, Cuz1/Ynl155w is proposed to protect cells from metalloid-induced proteotoxicity by delivering ubiquitinated substrates to Cdc48 and the proteasome for destruction.Entities:
Keywords: Proteasome; Protein Degradation; Protein Misfolding; Stress Response; Ubiquitin
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Year: 2013 PMID: 24297164 PMCID: PMC3894362 DOI: 10.1074/jbc.M113.534032
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157