Evidence map›Paper›PMID 26169355›Full record

ArticleThe Journal of cell biology2015

Rme-8 depletion perturbs Notch recycling and predisposes to pathogenic signaling.

Maria J Gomez-Lamarca, Laura A Snowdon, Ekatarina Seib, Thomas Klein, Sarah J Bray

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

20 citing papers in PubMed, 32 citations in OpenAlex.

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  18. Extracellular vesicle budding is inhibited by redundant regulators of TAT-5 flippase localization and phospholipid asymmetry.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Maria J Gomez-LamarcaDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, England, UK.
Laura A SnowdonDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, England, UK.
Ekatarina SeibInstitute of Genetics, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Thomas KleinInstitute of Genetics, Heinrich Heine University Düsseldorf, 40225 Düsseldorf, Germany.
Sarah J BrayDepartment of Physiology, Development and Neuroscience, University of Cambridge, Cambridge CB2 3DY, England, UK sjb32@cam.ac.uk.
University of Cambridge · GBHeinrich Heine University Düsseldorf · DE

Funding

Drosophila Transgenic RNAi Resource ProjectR01GM084947 · NIGMS · HARVARD MEDICAL SCHOOL · PI PERRIMON, NORBERT · 2008 to 2019
$9.8M
Biotechnology and Biological Sciences Research CouncilMedical Research Council G0800034Medical Research Council MR/L007177/1NIGMS NIH HHS R01 GM084947
6 · The paper itself

Abstract

Notch signaling is a major regulator of cell fate, proliferation, and differentiation. Like other signaling pathways, its activity is strongly influenced by intracellular trafficking. Besides contributing to signal activation and down-regulation, differential fluxes between trafficking routes can cause aberrant Notch pathway activation. Investigating the function of the retromer-associated DNAJ protein Rme-8 in vivo, we demonstrate a critical role in regulating Notch receptor recycling. In the absence of Rme-8, Notch accumulated in enlarged tubulated Rab4-positive endosomes, and as a consequence, signaling was compromised. Strikingly, when the retromer component Vps26 was depleted at the same time, Notch no longer accumulated and instead was ectopically activated. Likewise, depletion of ESCRT-0 components Hrs or Stam in combination with Rme-8 also led to high levels of ectopic Notch activity. Together, these results highlight the importance of Rme-8 in coordinating normal endocytic recycling route and reveal that its absence predisposes toward conditions in which pathological Notch signaling can occur.

Indexed as

AnimalsDisintegrinsDrosophila melanogasterDrosophila ProteinsEndosomal Sorting Complexes Required for TransportGene Knockdown TechniquesMetalloendopeptidasesProtein TransportReceptors, NotchSignal TransductionVesicular Transport ProteinsWnt1 ProteinDisintegrinsDrosophila ProteinsEndosomal Sorting Complexes Required for TransportKUZ protein, DrosophilaMetalloendopeptidasesN protein, DrosophilaReceptors, NotchRme-8 protein, DrosophilaVesicular Transport ProteinsVps26 protein, Drosophilawg protein, DrosophilaWnt1 Protein

Identifiers

PMID26169355
PMCPMC4508892
OpenAlexW2995932662

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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 OpenQuestion graph.