Evidence map›Paper›PMID 12847087›Full record

ArticleThe Journal of cell biology2003

Hrs regulates early endosome fusion by inhibiting formation of an endosomal SNARE complex.

Wei Sun, Qing Yan, Thomas A Vida, Andrew J Bean

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

44 citing papers in PubMed, 96 citations in OpenAlex.

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  8. Diminished Neuronal ESCRT-0 Function Exacerbates AMPA Receptor Derangement and Accelerates Prion-Induced Neurodegeneration.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
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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

4 authors at 1 institution in 1 country.

Wei SunThe University of Texas Health Science Center, Dept. of Neurobiology and Anatomy, 6431 Fannin Street, MSB 7.208, Houston, TX 77030, USA.
Qing Yan
Thomas A Vida
Andrew J Bean
The University of Texas Health Science Center at Houston · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
MOLECULAR MECHANISMS OF NEUROTRANSMITTER SECRETIONR01MH058920 · NIMH · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI BEAN, ANDREW J · 1998 to 2010
$2.9M
MECHANISMS OF ENDOSOME TO LYSOSOME TRANSPORT IN YEASTR01GM052092 · NIGMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI VIDA, THOMAS A · 1995 to 2005
$947k
NCI NIH HHS CA 16672NCI NIH HHS P30 CA016672NIGMS NIH HHS GM 52092NIGMS NIH HHS R01 GM052092NIMH NIH HHS MH 58920NIMH NIH HHS R01 MH058920
6 · The paper itself

Abstract

Movement through the endocytic pathway occurs principally via a series of membrane fusion and fission reactions that allow sorting of molecules to be recycled from those to be degraded. Endosome fusion is dependent on SNARE proteins, although the nature of the proteins involved and their regulation has not been fully elucidated. We found that the endosome-associated hepatocyte responsive serum phosphoprotein (Hrs) inhibited the homotypic fusion of early endosomes. A region of Hrs predicted to form a coiled coil required for binding the Q-SNARE, SNAP-25, mimicked the inhibition of endosome fusion produced by full-length Hrs, and was sufficient for endosome binding. SNAP-25, syntaxin 13, and VAMP2 were bound from rat brain membranes to the Hrs coiled-coil domain. Syntaxin 13 inhibited early endosomal fusion and botulinum toxin/E inhibition of early endosomal fusion was reversed by addition of SNAP-25(150-206), confirming a role for syntaxin 13, and establishing a role for SNAP-25 in endosomal fusion. Hrs inhibited formation of the syntaxin 13-SNAP-25-VAMP2 complex by displacing VAMP2 from the complex. These data suggest that SNAP-25 is a receptor for Hrs on early endosomal membranes and that the binding of Hrs to SNAP-25 on endosomal membranes inhibits formation of a SNARE complex required for homotypic endosome fusion.

Indexed as

Vesicular Transport ProteinsAnimalsEndocytosisEndosomal Sorting Complexes Required for TransportEndosomesEukaryotic CellsFluorescence Resonance Energy TransferHeLa CellsHumansIntracellular MembranesMacromolecular SubstancesMembrane FusionMembrane ProteinsModels, BiologicalNerve Tissue ProteinsPhosphoproteinsEndosomal Sorting Complexes Required for Transporthepatocyte growth factor-regulated tyrosine kinase substrateMacromolecular SubstancesMembrane ProteinsNerve Tissue ProteinsPhosphoproteinsQa-SNARE ProteinsR-SNARE ProteinsSNAP25 protein, humanSnap25 protein, ratSNARE ProteinsSynaptosomal-Associated Protein 25Vesicular Transport Proteins

Identifiers

PMID12847087
PMCPMC2172712
OpenAlexW2129349918

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.