Abstract

Elimination of misfolded proteins from the endoplasmic reticulum (ER) by ER-associated degradation involves substrate retrotranslocation from the ER lumen into the cytosol for degradation by the proteasome. For many substrates, retrotranslocation requires the action of ubiquitinating enzymes, which polyubiquitinate substrates emerging from the ER lumen, and of the p97-Ufd1-Npl4 ATPase complex, which hydrolyzes ATP to dislocate polyubiquitinated substrates into the cytosol. Polypeptides extracted by p97 are eventually transferred to the proteasome for destruction. In mammalian cells, ERAD can be blocked by a chemical inhibitor termed Eeyarestatin I, but the mechanism of EerI action is unclear. Here we report that EerI can associate with a p97 complex to inhibit ERAD. The interaction of EerI with the p97 complex appears to negatively influence a deubiquitinating process that is mediated by p97-associated deubiquitinating enzymes. We further show that ataxin-3, a p97-associated deubiquitinating enzyme previously implicated in ER-associated degradation, is among those affected. Interestingly, p97-associated deubiquitination is also involved in degradation of a soluble substrate. Our analyses establish a role for a novel deubiquitinating process in proteasome-dependent protein turnover.

Highlights

  • In eukaryotic cells the ubiquitin proteasome system (UPS)2 plays pivotal roles in many protein quality control pathways including the elimination of misfolded proteins from the endoplasmic reticulum (ER) [1,2,3]

  • P97 can be recruited to the ER membrane via association with two membrane proteins, Derlin and VIMP, which mediate the transport of a subset of substrates to the cytosol [26,27,28,29,30,31,32]

  • We recently reported that the degradation of several ER-associated protein degradation (ERAD) substrates is regulated by a p97-associated deubiquitinating enzyme (DUB) named ataxin-3, which may be part of the substrate delivery system [44]

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Summary

Eeyarestatin I Inhibits Deubiquitination

Cell Lines—A9 cells (stably expressing US11 and HA-tagged heavy chain) were described previously [45]. TG12 cells (stably expressing TCR␣-GFP) were a generous gift of Dr R. GFP␮, a retroviral packaging cell line (GP2-293 cells) was co-transfected with pLNCX2-HA-GFP␮. 72 h after transfection, and used to infect 373MG cells. HA-GFP␮-expressing cells were selected by neomycin (500 ␮g/ml). Mammalian Cell Culture, Transient Gene Expression, Fractionation, and Coimmunoprecipitation—Astrocytoma cells and 293T cells were maintained according to standard procedures. Transfections in 293T cells were done with Trans. Cytoma cells were performed as described previously [36]. Astrocytoma cells expressing US11 were treated with chemicals as indicated in the figure legends. Cells were labeled with 27.5 ␮Ci of [35S]methionine per 1.0 ϫ 106 cells. The cells were permeabilized by addition of 0.028%

EXPERIMENTAL PROCEDURES
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