Evidence map›Paper›PMID 32322926›Full record

ArticleCellular and molecular life sciences : CMLS2021

Receptor-mediated endocytosis 8 (RME-8)/DNAJC13 is a novel positive modulator of autophagy and stabilizes cellular protein homeostasis.

Anna S Besemer, Joanna Maus, Mirjam D A Ax, Anna Stein, Stella Vo, Christian Freese, Karsten Nalbach, Christian von Hilchen, Ines F Pfalzgraf, Ingrid Koziollek-Drechsler and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular and molecular life sciences : CMLS, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 32 citations in OpenAlex.

  1. Article
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  5. SNX-3 confers lysosomal fusion-competence to sustain basal autophagy.Cellular and molecular life sciences : CMLS · 2026
    Article
  6. Review
  7. Article
  8. Article
  9. Progress on multifunctional transmembrane protein ATG9A.Cell communication and signaling : CCS · 2025
    Review
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  11. Article
  12. Article
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  14. Article
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  18. Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors at 1 institution in 1 country.

Anna S BesemerInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Joanna MausInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Mirjam D A AxInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Anna SteinInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Stella VoInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Christian FreeseInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Karsten NalbachInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Christian von HilchenInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Ines F PfalzgrafInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Ingrid Koziollek-DrechslerInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Beate SilvaInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Heike HuesmannInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Fatima BoukhalloukInstitute of Medical Microbiology and Hygiene, University Medical Center of the Johannes Gutenberg-University, 55101 Mainz, Germany.
Luise FlorinInstitute for Virology and Research Center for Immunotherapy (FZI), University Medical Center of the Johannes Gutenberg-University, 55101 Mainz, Germany.
Andreas KernInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany.
Christian BehlInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany. cbehl@uni-mainz.de.
Albrecht M ClementInstitute of Pathobiochemistry, University Medical Center of the Johannes Gutenberg-University, Duesbergweg 6, 55128, Mainz, Germany. clement@uni-mainz.de.ORCID http://orcid.org/0000-0002-6058-7507
Johannes Gutenberg University Mainz · DE

Funding

DFG CRC1080DFG CRC1177DFG FL 696/2-1
6 · The paper itself

Abstract

The 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.

Indexed as

AutophagyProteostasisAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsHEK293 CellsHeLa CellsHumansMolecular ChaperonesProtein AggregatesCaenorhabditis elegans ProteinsDNAJC13 protein, humanMolecular ChaperonesProtein AggregatesRME-8 protein, C elegansATG9AAutophagyC. elegansDNAJC13ProteostasisRecycling endosomeRME-8

Identifiers

PMID32322926
PMCPMC7873018
OpenAlexW3019923217

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.