Journal of Biological Chemistry
Volume 284, Issue 16, 17 April 2009, Pages 10537-10545
Journal home page for Journal of Biological Chemistry

Protein Synthesis, Post-Translational Modification, and Degradation
The Ubiquitin Ligase E6-AP Is Induced and Recruited to Aggresomes in Response to Proteasome Inhibition and May Be Involved in the Ubiquitination of Hsp70-bound Misfolded Proteins*

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Cells are equipped with an efficient quality control system to selectively eliminate abnormally folded and damaged proteins. Initially the cell tries to refold the unfolded proteins with the help of molecular chaperones, and failure to refold leads to their degradation by the ubiquitin proteasome system. But how this proteolytic machinery recognizes the abnormally folded proteins is poorly understood. Here, we report that E6-AP, a HECT domain family ubiquitin ligase implicated in Angelman syndrome, interacts with the substrate binding domain of Hsp70/Hsc70 chaperones and promotes the degradation of chaperone bound substrates. The expression of E6-AP was dramatically induced under a variety of stresses, and overexpression of E6-AP was found to protect against endoplasmic reticulum stress-induced cell death. The inhibition of proteasome function not only increases the expression of E6-AP but also causes its redistribution around microtubule-organizing center, a subcellular structure for the degradation of the cytoplasmic misfolded proteins. E6-AP is also recruited to aggresomes containing the cystic fibrosis transmembrane conductance regulator or expanded polyglutamine proteins. Finally, we demonstrate that E6-AP ubiquitinates misfolded luciferase that is bound by Hsp70. Our results suggest that E6-AP functions as a cellular quality control ubiquitin ligase and, therefore, can be implicated not only in the pathogenesis of Angelman syndrome but also in the biology of neurodegenerative disorders involving protein aggregation.

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The abbreviations used are: UPS, ubiquitin proteasome system; CHIP, C terminus of Hsp70-interacting protein; MTT, 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide; HECT, homologous to E6-AP C terminus; ER, endoplasmic reticulum; CFTR, cystic fibrosis transmembrane conductance regulator; MTOC, microtubule-organizing center; HD, Huntington disease; GFP, green fluorescence protein; E1, ubiquitin-activating enzyme; E2, ubiquitin carrier protein; E3, ubiquitin-protein isopeptide ligase; GAPDH, glyceraldehyde-3-phosphate dehydrogenase.

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This work was supported by the Department of Biotechnology, Government of India.

The on-line version of this article (available at http://www.jbc.org) contains supplemental Figs. S1 and S2.

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Supported by research fellowship from Council of Scientific and Industrial Research, Government of India.