Evidence map›Paper›PMID 30986258›Full record

ArticlePloS one2019

Function of Golgi-centrosome proximity in RPE-1 cells.

Kati Tormanen, Celine Ton, Barbara M Waring, Kevin Wang, Christine Sütterlin

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

11 citing papers in PubMed, 15 citations in OpenAlex.

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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

5 authors at 1 institution in 1 country.

Kati TormanenDepartment of Developmental and Cell Biology, University of California, Irvine, Irvine, California, United States of America.ORCID 0000-0002-9240-9406
Celine TonDepartment of Developmental and Cell Biology, University of California, Irvine, Irvine, California, United States of America.
Barbara M WaringDepartment of Developmental and Cell Biology, University of California, Irvine, Irvine, California, United States of America.
Kevin WangDepartment of Developmental and Cell Biology, University of California, Irvine, Irvine, California, United States of America.
Christine SütterlinDepartment of Developmental and Cell Biology, University of California, Irvine, Irvine, California, United States of America.
University of California, Irvine · US

Funding

MEDICAL SCIENTIST TRAINING PROGRAMT32GM008620 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GOLDIN, ALAN L · 1999 to 2023
$8.1M
Mechanism of centrosome regulation from the GolgiR01GM089913 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI SUETTERLIN, CHRISTINE · 2010 to 2014
$1.4M
NIGMS NIH HHS R01 GM089913NIGMS NIH HHS T32 GM008620
6 · The paper itself

Abstract

The close physical proximity between the Golgi and the centrosome is a unique feature of mammalian cells that has baffled scientists for years. Several knockdown and overexpression studies have linked the spatial relationship between these two organelles to the control of directional protein transport, directional migration, ciliogenesis and mitotic entry. However, most of these conditions have not only separated these two organelles, but also caused extensive fragmentation of the Golgi, making it difficult to dissect the specific contribution of Golgi-centrosome proximity. In this study, we present our results with stable retinal pigment epithelial (RPE-1) cell lines in which GM130 was knocked out using a CRISPR/Cas9 approach. While Golgi and centrosome organization appeared mostly intact in cells lacking GM130, there was a clear separation of these organelles from each other. We show that GM130 may control Golgi-centrosome proximity by anchoring AKAP450 to the Golgi. We also provide evidence that the physical proximity between these two organelles is dispensable for protein transport, cell migration, and ciliogenesis. These results suggest that Golgi-centrosome proximity per se is not necessary for the normal function of RPE-1 cells.

Indexed as

A Kinase Anchor ProteinsAutoantigensCell LineCentrosomeCRISPR-Cas SystemsCytoskeletal ProteinsEpithelial CellsGene DeletionGolgi ApparatusHumansMembrane ProteinsRetinal Pigment EpitheliumAKAP9 protein, humanA Kinase Anchor ProteinsAutoantigensCytoskeletal ProteinsGolgin subfamily A member 2Membrane Proteins

Identifiers

PMID30986258
PMCPMC6464164
OpenAlexW2936312326

What OpenQuestion holds

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LicenceCC BY
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.