Evidence map›Paper›PMID 16251359›Full record

ArticleMolecular biology of the cell2006

Cis-Golgi matrix proteins move directly to endoplasmic reticulum exit sites by association with tubules.

Gonzalo A Mardones, Christopher M Snyder, Kathryn E Howell

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
1.6field-weighted citation impact, top 19% 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

34 citing papers in PubMed, 59 citations in OpenAlex.

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  16. Golgi compartmentation and identity.Current opinion in cell biology · 2014
    Review
  17. 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

3 authors at 1 institution in 1 country.

Gonzalo A MardonesDepartment of Cell and Developmental Biology, University of Colorado School of Medicine, Aurora, CO 80045, USA.
Christopher M Snyder
Kathryn E Howell
University of Colorado Denver · US

Funding

The functional role of microRNAs in the normal mammary glandP01HD038129 · NICHD · UNIVERSITY OF COLORADO DENVER · PI ANDERSON, STEVEN M · 2000 to 2015
$15.2M
TARGETING OF VESICLES FROM THE TRANS GOLGI NETWORKR01GM042629 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI HOWELL, KATHRYN ELIZABETH · 1990 to 2002
$838k
NICHD NIH HHS P01 HD038129NIGMS NIH HHS GM-42629NIGMS NIH HHS R01 GM042629PHS HHS CHD038129
6 · The paper itself

Abstract

The role of cis-medial Golgi matrix proteins in retrograde traffic is poorly understood. We have used imaging techniques to understand the relationship between the cis-medial Golgi matrix and transmembrane proteins during retrograde traffic in control and brefeldin A (BFA)-treated cells. All five of the cis-medial matrix proteins tested were associated with retrograde tubules within 2-3 min of initiation of tubule formation. Then, at later time points (3-10 min), transmembrane proteins are apparent in the same tubules. Strikingly, both the matrix proteins and the transmembrane proteins moved directly to endoplasmic reticulum (ER) exit sites labeled with p58 and Sec13, and there seemed to be a specific interaction between the ER exit sites and the tips or branch points of the tubules enriched for the matrix proteins. After the initial interaction, Golgi matrix proteins accumulated rapidly (5-10 min) at ER exit sites, and Golgi transmembrane proteins accumulated at the same sites approximately 2 h later. Our data suggest that Golgi cis-medial matrix proteins participate in Golgi-to-ER traffic and play a novel role in tubule formation and targeting.

Indexed as

AnimalsBrefeldin ACell LineEndoplasmic ReticulumGolgi ApparatusIntracellular MembranesProteinsProtein TransportRatsBrefeldin AProteins

Identifiers

PMID16251359
PMCPMC1345687
OpenAlexW2083835208

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.