Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/27893
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorLim, J-
dc.creatorLachenmayer, ML-
dc.creatorWu, S-
dc.creatorLiu, W-
dc.creatorKundu, M-
dc.creatorWang, R-
dc.creatorKomatsu, M-
dc.creatorOh, YJ-
dc.creatorZhao, Y-
dc.creatorYue, Z-
dc.date.accessioned2015-07-13T10:34:55Z-
dc.date.available2015-07-13T10:34:55Z-
dc.identifier.issn1553-7390en_US
dc.identifier.urihttp://hdl.handle.net/10397/27893-
dc.language.isoenen_US
dc.publisherPublic Library of Scienceen_US
dc.rights© 2015 Lim et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are crediteden_US
dc.rightsThe following publication: Lim J, Lachenmayer ML, Wu S, Liu W, Kundu M, Wang R, et al. (2015) Proteotoxic Stress Induces Phosphorylation of p62/SQSTM1 by ULK1 to Regulate Selective Autophagic Clearance of Protein Aggregates. PLoS Genet 11(2): e1004987 is available at https://doi.org/10.1371/journal.pgen.1004987en_US
dc.titleProteotoxic stress induces phosphorylation of p62/SQSTM1 by ULK1 to regulate selective autophagic clearance of protein aggregatesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage1en_US
dc.identifier.epage28en_US
dc.identifier.volume11en_US
dc.identifier.issue2en_US
dc.identifier.doi10.1371/journal.pgen.1004987en_US
dcterms.abstractDisruption of proteostasis, or protein homeostasis, is often associated with aberrant accumulation of misfolded proteins or protein aggregates. Autophagy offers protection to cells by removing toxic protein aggregates and injured organelles in response to proteotoxic stress. However, the exact mechanism whereby autophagy recognizes and degrades misfolded or aggregated proteins has yet to be elucidated. Mounting evidence demonstrates the selectivity of autophagy, which is mediated through autophagy receptor proteins (e.g. p62/SQSTM1) linking autophagy cargos and autophagosomes. Here we report that proteotoxic stress imposed by the proteasome inhibition or expression of polyglutamine expanded huntingtin (polyQ-Htt) induces p62 phosphorylation at its ubiquitin-association (UBA) domain that regulates its binding to ubiquitinated proteins. We find that autophagy-related kinase ULK1 phosphorylates p62 at a novel phosphorylation site S409 in UBA domain. Interestingly, phosphorylation of p62 by ULK1 does not occur upon nutrient starvation, in spite of its role in canonical autophagy signaling. ULK1 also phosphorylates S405, while S409 phosphorylation critically regulates S405 phosphorylation. We find that S409 phosphorylation destabilizes the UBA dimer interface, and increases binding affinity of p62 to ubiquitin. Furthermore, lack of S409 phosphorylation causes accumulation of p62, aberrant localization of autophagy proteins and inhibition of the clearance of ubiquitinated proteins or polyQ-Htt. Therefore, our data provide mechanistic insights into the regulation of selective autophagy by ULK1 and p62 upon proteotoxic stress. Our study suggests a potential novel drug target in developing autophagy-based therapeutics for the treatment of proteinopathies including Huntington’s disease.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationPLoS genetics, 2015, v. 11, no. 2, e1004987, p. 1-28-
dcterms.isPartOfPLoS Genetics-
dcterms.issued2015-
dc.identifier.scopus2-s2.0-84924415434-
dc.identifier.pmid25723488-
dc.identifier.rosgroupid2014004779-
dc.description.ros2014-2015 > Academic research: refereed > Publication in refereed journalen_US
dc.description.validate201810_a bcmaen_US
dc.description.oaVersion of Recorden_US
dc.identifier.FolderNumberOA_IR/PIRAen_US
dc.description.pubStatusPublisheden_US
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