Evidence map›Paper›PMID 36640308›Full record

ArticleCell reports2023

Consecutive functions of small GTPases guide HOPS-mediated tethering of late endosomes and lysosomes.

Ariane Schleinitz, Lara-Alina Pöttgen, Tal Keren-Kaplan, Jing Pu, Paul Saftig, Juan S Bonifacino, Albert Haas, Andreas Jeschke

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
10.4field-weighted citation impact, top 1% 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

32 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
  2. Late Endosome Transport by RILP-RAB7A Promotes Dendrite Arborization Independently of Degradation.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
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  8. Late endosome transport by RILP-RAB7A promotes dendrite arborization.bioRxiv : the preprint server for biology · 2025
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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

8 authors at 4 institutions in 2 countries.

Ariane SchleinitzCell Biology Institute, University of Bonn, 53121 Bonn, Germany.
Lara-Alina PöttgenCell Biology Institute, University of Bonn, 53121 Bonn, Germany.
Tal Keren-KaplanNeurosciences and Cellular and Structural Biology Division, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Jing PuDepartment of Molecular Genetics and Microbiology, and Autophagy, Inflammation, and Metabolism, Center of Biomedical Research Excellence, University of New Mexico, Albuquerque, NM 87131, USA.
Paul SaftigBiochemical Institute, University of Kiel, 24118 Kiel, Germany.
Juan S BonifacinoNeurosciences and Cellular and Structural Biology Division, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.
Albert HaasCell Biology Institute, University of Bonn, 53121 Bonn, Germany. Electronic address: ahaas@uni-bonn.de.
Andreas JeschkeCell Biology Institute, University of Bonn, 53121 Bonn, Germany. Electronic address: jeschke@uni-bonn.de.
University of Bonn · DENational Institutes of Health · USChristian-Albrechts-Universität zu Kiel · DEUniversity of New Mexico · US

Funding

Protein Trafficking In The Endosomal-Lysosomal SystemZIAHD001607 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BONIFACINO, JUAN · 2009 to 2025
$48.3M
REGULATION OF THE FATE OF NEWLY SYNTHESIZED PROTEINSZ01HD001607 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI BONIFACINO, JUAN · 1991 to 2008
$4.4M
Lysosome‐Lipid Droplet Interactions in Fatty Acid MetabolismR35GM147419 · NIGMS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI Jing Pu · 2022 to 2026
$1.9M
Intramural NIH HHS Z01 HD001607Intramural NIH HHS ZIA HD001607NIGMS NIH HHS R35 GM147419
6 · The paper itself

Abstract

The transfer of endocytosed cargoes to lysosomes (LYSs) requires HOPS, a multiprotein complex that tethers late endosomes (LEs) to LYSs before fusion. Many proteins interact with HOPS on LEs/LYSs. However, it is not clear whether these HOPS interactors localize to LEs or LYSs or how they participate in tethering. Here, we biochemically characterized endosomes purified from untreated or experimentally manipulated cells to put HOPS and interacting proteins in order and to establish their functional interdependence. Our results assign Rab2a and Rab7 to LEs and Arl8 and BORC to LYSs and show that HOPS drives LE-LYS fusion by bridging late endosomal Rab2a with lysosomal BORC-anchored Arl8. We further show that Rab7 is absent from sites of HOPS-dependent tethering but promotes fusion by moving LEs toward LYSs via dynein. Thus, our study identifies the topology of the machinery for LE-LYS tethering and elucidates the role of different small GTPases in the process.

Indexed as

EndocytosisEndosomesLysosomesMembrane Fusionrab GTP-Binding Proteinsrab GTP-Binding ProteinsautophagosomeautophagyCP: Cell biologydyneinendolysosomelysosome reformationmembrane fusionmembrane tetheringphagocytosisphosphoinositidesprotein trafficking

Identifiers

PMID36640308
PMCPMC10018218
OpenAlexW4313491541

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.