Evidence map›Paper›PMID 11101519›Full record

ArticleThe EMBO journal2000

Immobilization of the early secretory pathway by a virus glycoprotein that binds to microtubules.

A Xu, A R Bellamy, J A Taylor

Abstract read
In one paragraph

Article in The EMBO journal, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
–field-weighted citation impact
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

41 citing papers in PubMed.

  1. Article
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  6. Understanding the penetrance of intrinsic protein disorder in rotavirus proteome.International journal of biological macromolecules · 2020
    Article
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  8. 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

3 authors.

A XuMicrobiology and Virology Research Group, School of Biological Sciences, University of Auckland, Private Bag 92019, Auckland, New Zealand.
A R Bellamy
J A Taylor

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Membrane trafficking from the endoplasmic reticulum (ER) to the Golgi complex is mediated by pleiomorphic carrier vesicles that are driven along microtubule tracks by the action of motor proteins. Here we describe how NSP4, a rotavirus membrane glycoprotein, binds to microtubules and blocks ER-to-Golgi trafficking in vivo. NSP4 accumulates in a post-ER, microtubule-associated membrane compartment and prevents targeting of vesicular stomatitis virus glycoprotein (VSV-G) at a pre-Golgi step. NSP4 also redistributes beta-COP and ERGIC53, markers of a vesicular compartment that dynamically cycles between the ER and Golgi, to structures aligned along linear tracks radiating throughout the cytoplasm. This block in membrane trafficking is released when microtubules are depolymerized with nocodazole, indicating that vesicles containing NSP4 are tethered to the microtubule cytoskeleton. Disruption of microtubule-mediated membrane transport by a viral glycoprotein may represent a novel pathogenic mechanism and provides a new experimental tool for the dissection of early steps in exocytic transport.

Indexed as

DNA-Directed RNA PolymerasesMannose-Binding LectinsMembrane GlycoproteinsAnimalsAntineoplastic AgentsAntineoplastic Agents, PhytogenicCell LineCell MembraneCoatomer ProteinCOS CellsCytoplasmCytoskeletonDose-Response Relationship, DrugElectrophoresis, Polyacrylamide GelEndoplasmic ReticulumExocytosisAntineoplastic AgentsAntineoplastic Agents, PhytogenicCoatomer ProteinDNA-Directed RNA PolymerasesGlutathione TransferaseGlycoproteinsGlycoside HydrolasesG protein, vesicular stomatitis virusMannose-Binding LectinsMembrane GlycoproteinsMembrane ProteinsNocodazolePaclitaxelRecombinant Fusion ProteinsTubulinViral Envelope ProteinsViral Nonstructural Proteins

Identifiers

PMID11101519
PMCPMC305877

What OpenQuestion holds

Textmetadata
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.