Evidence map›Paper›PMID 25847539›Full record

ArticleThe Journal of cell biology2015

G3BP1 promotes stress-induced RNA granule interactions to preserve polyadenylated mRNA.

Anaïs Aulas, Guillaume Caron, Christos G Gkogkas, Nguyen-Vi Mohamed, Laurie Destroismaisons, Nahum Sonenberg, Nicole Leclerc, J Alex Parker, Christine Vande Velde

Open 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. Cited by 66 papers.

0numbers the graph read from it
0cells of the map it votes in
66citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

66 citing papers in PubMed, 140 citations in OpenAlex.

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  19. Inhibition of Nonsense-Mediated Decay Induces Nociceptive Sensitization through Activation of the Integrated Stress Response.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  20. Article

6 more citing papers are in PubMed but not listed here.

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

9 authors at 4 institutions in 2 countries.

Anaïs AulasCentre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada Centre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada.
Guillaume CaronCentre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada Centre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada.
Christos G GkogkasPatrick Wild Centre and Centre for Integrative Physiology, University of Edinburgh, Edinburgh EH8 9XD, Scotland, UK Patrick Wild Centre and Centre for Integrative Physiology, University of Edinburgh, Edinburgh EH8 9XD, Scotland, UK.
Nguyen-Vi MohamedCentre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada Centre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada.
Laurie DestroismaisonsCentre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada.
Nahum SonenbergDepartment of Biochemistry and Goodman Cancer Research Centre, McGill University, Montréal, Quebec H3A 1A3, Canada Department of Biochemistry and Goodman Cancer Research Centre, McGill University, Montréal, Quebec H3A 1A3, Canada.
Nicole LeclercCentre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada Centre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada.
J Alex ParkerCentre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada Centre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada.
Christine Vande VeldeCentre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada Centre de recherché du Centre Hospitalier de l'Université de Montréal (CRCHUM), Department of Biochemistry, and Department of Neuroscience, Université de Montréal, Montréal, QC, H2X 0A9, Canada c.vande.velde@umontreal.ca.
Université de Montréal · CACentre Hospitalier de l’Université de Montréal · CAMcGill University · CAUniversity of Edinburgh · GB

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

G3BP1, a target of TDP-43, is required for normal stress granule (SG) assembly, but the functional consequences of failed SG assembly remain unknown. Here, using both transformed cell lines and primary neurons, we investigated the functional impact of this disruption in SG dynamics. While stress-induced translational repression and recruitment of key SG proteins was undisturbed, depletion of G3BP1 or its upstream regulator TDP-43 disturbed normal interactions between SGs and processing bodies (PBs). This was concomitant with decreased SG size, reduced SG-PB docking, and impaired preservation of polyadenylated mRNA. Reintroduction of G3BP1 alone was sufficient to rescue all of these phenotypes, indicating that G3BP1 is essential for normal SG-PB interactions and SG function.

Indexed as

AnimalsCarrier ProteinsCytoplasmic GranulesDNA-Binding ProteinsDNA HelicasesHeLa CellsHumansMice, Inbred C57BLPolyadenylationPoly-ADP-Ribose Binding ProteinsProtein BiosynthesisRNA HelicasesRNA, MessengerRNA Recognition Motif ProteinsRNA StabilityStress, PhysiologicalCarrier ProteinsDNA-Binding ProteinsDNA HelicasesG3BP1 protein, humanPoly-ADP-Ribose Binding ProteinsRNA HelicasesRNA, MessengerRNA Recognition Motif ProteinsTARDBP protein, human

Identifiers

PMID25847539
PMCPMC4395486
OpenAlexW1979042130

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.