Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-5877
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dc.contributor.authorBesemer, Anna S.-
dc.contributor.authorMaus, Joanna-
dc.contributor.authorAx, Mirjam D. A.-
dc.contributor.authorStein, Anna-
dc.contributor.authorVo, Stella-
dc.contributor.authorFreese, Christian-
dc.contributor.authorNalbach, Karsten-
dc.contributor.authorHilchen, Christian von-
dc.contributor.authorPfalzgraf, Ines F.-
dc.contributor.authorKoziollek-Drechsler, Ingrid-
dc.contributor.authorSilva, Beate-
dc.contributor.authorHuesmann, Heike-
dc.contributor.authorBoukhallouk, Fatima-
dc.contributor.authorFlorin, Luise-
dc.contributor.authorKern, Andreas-
dc.contributor.authorBehl, Christian-
dc.contributor.authorClement, Albrecht M.-
dc.date.accessioned2021-05-10T07:33:42Z-
dc.date.available2021-05-10T07:33:42Z-
dc.date.issued2021-
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/5886-
dc.description.abstractThe cellular protein homeostasis (proteostasis) network responds effectively to insults. In a functional screen in C. elegans, we recently identified the gene receptor-mediated endocytosis 8 (rme-8; human ortholog: DNAJC13) as a component of the proteostasis network. Accumulation of aggregation-prone proteins, such as amyloid-β 42 (Aβ), α-synuclein, or mutant Cu/Zn-superoxide dismutase (SOD1), were aggravated upon the knockdown of rme-8/DNAJC13 in C. elegans and in human cell lines, respectively. DNAJC13 is involved in endosomal protein trafficking and associated with the retromer and the WASH complex. As both complexes have been linked to autophagy, we investigated the role of DNAJC13 in this degradative pathway. In knockdown and overexpression experiments, DNAJC13 acts as a positive modulator of autophagy. In contrast, the overexpression of the Parkinson’s disease-associated mutant DNAJC13(N855S) did not enhance autophagy. Reduced DNAJC13 levels affected ATG9A localization at and its transport from the recycling endosome. As a consequence, ATG9A co-localization at LC3B-positive puncta under steady-state and autophagy-induced conditions is impaired. These data demonstrate a novel function of RME-8/DNAJC13 in cellular homeostasis by modulating ATG9A trafficking and autophagy.en_GB
dc.language.isoengde
dc.rightsCC BY*
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/*
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.subject.ddc570 Biowissenschaftende_DE
dc.subject.ddc570 Life sciencesen_GB
dc.subject.ddc610 Medizinde_DE
dc.subject.ddc610 Medical sciencesen_GB
dc.titleReceptor-mediated endocytosis 8 (RME-8)/DNAJC13 is a novel positive modulator of autophagy and stabilizes cellular protein homeostasisen_GB
dc.typeZeitschriftenaufsatzde
dc.identifier.doihttp://doi.org/10.25358/openscience-5877-
jgu.type.dinitypearticleen_GB
jgu.type.versionPublished versionde
jgu.type.resourceTextde
jgu.organisation.departmentFB 04 Medizinde
jgu.organisation.number2700-
jgu.organisation.nameJohannes Gutenberg-Universität Mainz-
jgu.rights.accessrightsopenAccess-
jgu.journal.titleCellular and molecular life sciencesde
jgu.journal.volume78de
jgu.pages.start645de
jgu.pages.end660de
jgu.publisher.year2021-
jgu.publisher.nameSpringer International Publishing AGde
jgu.publisher.placeCham (ZG)de
jgu.publisher.urihttps://doi.org/10.1007/s00018-020-03521-yde
jgu.publisher.issn1420-9071de
jgu.organisation.placeMainz-
jgu.subject.ddccode540de
jgu.subject.ddccode570de
jgu.subject.ddccode610de
jgu.publisher.doi10.1007/s00018-020-03521-y
jgu.organisation.rorhttps://ror.org/023b0x485
Appears in collections:JGU-Publikationen

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